No retraction, correction or concern found when last checked on Oct 19, 2026.
Determinants of metastatic competency in colorectal cancer
Daniele V. F. Tauriello, Alexandre Calon, Enza Lonardo and 1 more
Molecular Oncology · 2017 · Review · CC BY
Abstract
Colorectal cancer ( CRC ) is one of the most common cancer types and represents a major therapeutic challenge. Although initial events in colorectal carcinogenesis are relatively well characterized and treatment for early‐stage disease has significantly improved over the last decades, the mechanisms underlying metastasis – the main cause of death – remain poorly understood. Correspondingly, no effective therapy is currently available for advanced or metastatic disease. There is increasing evidence that colorectal cancer is hierarchically organized and sustained by cancer stem cells, in concert with various stromal cell types. Here, we review the interplay between cancer stem cells and their microenvironment in promoting metastasis and discuss recent insights relating to both patient prognosis and novel targeted treatment strategies. A better understanding of these topics may aid the prevention or reduction of metastatic burden.
Full text
From PubMed Central, U.S. National Library of Medicine, as current on Oct 19, 2026. Paragraph numbers are ours, so an answer can point at one.
American Joint Committee on Cancer
cancer‐associated fibroblast
consensus molecular subtype
colorectal cancer
colorectal cancer stem cell
circulating tumour DNA
cytotoxic T lymphocyte
epithelial–mesenchymal transition
endothelial–mesenchymal transition
hepatic stellate cell
intestinal stem cell
intratumoral heterogeneity
myeloid‐derived suppressor cell
metastatic stem cell
mesenchymal stem cell
microsatellite‐instable
stem cell
tumour‐associated macrophage
tumour‐associated neutrophil
tumour microenvironment
tumour, lymph node, metastasis
unfolded protein response
Introduction
Colorectal cancer (CRC) is one of the most frequent types of cancer worldwide, accounting for approximately 10% of all new cancer cases and 8.5% of all cancer deaths (Torre et al., 2015). Whereas the vast majority of primary cancers can be extirpated through surgical resection, only a fraction of the patients diagnosed with overt metastatic disease can be cured by surgery. About 20% of the patients with CRC present with metastasis at the time of diagnosis (stage IV). In addition, 35–45% of the patients with localized disease (stages II and III) succumb to recurrence within 5 years after surgery. Most of these relapses occur as metastases and are caused by residual tumour cells that have spread to distant organs prior to surgery. Clearly, current systemic therapies fail to eliminate latent disseminated tumour cells and are similarly ineffective in treating growing metastases, offering survival benefits of only a few months.
Metastasis is the spread of cancer to a distant organ, which in the case of patients with CRC involves mainly the liver and lungs. As described elsewhere (Massague and Obenauf, 2016; Oskarsson et al., 2014; Valastyan and Weinberg, 2011), to gain metastatic competence, cancer cells require the capacity to invade the surrounding tissues, survive in the circulation, colonize the foreign organ and eventually resume growth. Metastasis is an inefficient process owing to the fact that most tumour cells fail to acquire the necessary abilities to regenerate a tumour at a distant site (Massague and Obenauf, 2016; Oskarsson et al., 2014). Over the past few years, the main determinants of metastatic competence in CRC have begun to be characterized. In the absence of mutations that associate with the process of metastasis in CRC, it has become increasingly clear that the regeneration of the tumour in a foreign organ is tightly bound to the acquisition of a stemlike phenotype by cancer cells. These metastatic stem cells adopt multiple phenotypes and behaviours and critically depend on their interaction with the microenvironment to migrate, survive in the circulation and thrive in a foreign organ.
In Section 2, we will review the genetics of CRC development, to then discuss both the evidence that supports the notion of hierarchical organization throughout CRC progression and the ensuing implications in Section 5. We will also focus on the mechanisms involved in the multiple phenotypes and adaptations that tumour stem cells go through in the metastatic process. In Section 2.2, we will explore the current knowledge about the role of the tumour microenvironment in promoting and sustaining metastasis. This includes a dissection of the cell types and niches that support the survival and maintenance of metastatic stem cells, and an analysis of the ways that stromal features can improve disease prognosis. In Section 3, we will discuss the complexities and limitations imposed on clinical practice by the heterogeneous nature of both epithelial and stromal compartments. Finally, we will indicate how these emerging concepts are informing, and slowly transforming, therapeutic strategies to treat patients with metastatic disease.
From normal mucosa to colorectal cancer
The epithelium of the normal colon undergoes continuous renewal. At the base of glandular invaginations of the colonic mucosa, called crypts, a pool of rapidly diving intestinal stem cells (ISCs) sustains the homoeostatic regeneration of the epithelium throughout a lifetime (Clevers, 2013). Over the past decade, signals that regulate ISC renewal and proliferation have been extensively characterized: WNT, EGFR/MAPK and NOTCH signalling promote the undifferentiated proliferative state of ISCs in the niche, whereas BMP and TGF‐beta signalling induce cytostasis and differentiation (Clevers, 2013).
The elevated division rate of ISCs increases their probability to acquire mutations during DNA replication (Vogelstein et al., 2013). Additional environmental factors such as lifestyle, diet and microbiota can also greatly influence the transformation of the epithelium (Bishehsari et al., 2014). The most common genetic events in CRCs are alterations that inactivate the tumour suppressor gene APC. This triggers the constitutive activation of WNT signalling and imposes a continuous stemlike self‐renewing state at the onset of tumorigenesis, giving rise to benign outgrowths of the epithelium known as adenomas. Genetic experiments performed in mouse models support the hypothesis that Apc mutation in ISCs represents the origin of intestinal polyps (Barker et al., 2008; Tetteh et al., 2016), although chronic inflammation or dysregulation of BMP signalling has been shown to help convert non‐stem cells into CRC‐initiating cells (Davis et al., 2014; Schwitalla et al., 2013).
A small fraction of adenomas become progressively aggressive through acquisition of additional driver mutations, which mainly affect three additional signalling pathways (Cancer Genome Atlas Network, 2012; Seshagiri et al., 2012): (a) the MAPK pathway is often hit by activating mutations in KRAS, BRAF or PIK3CA and provides cell autonomous mitogenic and pro‐survival stimuli to cancer cells; (b) the p53 pathway is inactivated by mutations in the eponymous protein, or less commonly in ATM, facilitating acquisition of genomic instability; and (c) the TGF‐beta pathway is frequently silenced by loss‐of‐function mutations in TGFBR2, SMAD4, SMAD2 or SMAD3, which bypasses the suppressive effects of high TGF‐beta levels present in the tumour microenvironment (Fearon, 2011). Pioneer studies by Eric Fearon and Bert Vogelstein correlated these mutations with pathologically classifiable stages of adenoma malignancy and suggested a linear progression model, in which the compounding of the four mentioned pathway mutations associated with development of aggressive adenocarcinomas (Fearon and Vogelstein, 1990).
Acquisition of these mutations is a slow process, and consequently, the development of invasive CRC often takes decades (Jones et al., 2008; Vogelstein et al., 2013). Of note, the linear progression model based on four stepwise genetic alterations represents a simplification, as not every tumour carries genetic alterations in these four pathways or develops through the equivalent sequence of events. Moreover, full‐blown CRCs have a riche and complex mutational landscape that expands well beyond mutations in the four driver pathways (Cancer Genome Atlas Network, 2012; Seshagiri et al., 2012). Due to the acquisition of chromosomal instability or defects in the DNA mismatch repair system, tumours accumulate hundreds or even thousands of genetic alterations. Some of these are passenger mutations, as they do not confer advantages to tumour cells, but others drive the biology of the cancer and therefore give selective advantage. Beyond the context of the linear progression model, the role of many of these mutations remains poorly understood. Together, these issues of complexity and heterogeneity impinge upon the functional analysis of CRC and complicate the development and application of therapeutic approaches.
Progression to metastasis
As described above, the mutations that drive CRC progression affect the signalling pathways that regulate ISC behaviour, endowing cancer cells with self‐renewal and growth capacity, independently of crypt niche signals. Evidence obtained from the analysis of patient‐derived and CRISPR‐engineered CRC organoids has led to the hypothesis that acquisition of mutations in the four linear progression model pathways may be sufficient to facilitate the growth of tumour cells in unfavourable environments such as those encountered in foreign tissues (Drost et al., 2015; Fujii et al., 2016; Matano et al., 2015). Yet, while most CRCs carry genetic alterations in several of these four driver pathways, metastasis is a relatively inefficient process. This suggests that additional bottlenecks and dependencies limit the extent of tumour spread.
It is worth considering that most CRCs are invasive at the time of diagnosis and, therefore, have had the opportunity to shed cells into circulation for months or longer. When disseminating CRC cells enter the portal circulation, they are transported to the liver sinusoids within minutes and can home into the liver parenchyma because of vessel fenestration. In the case of pulmonary metastases, CRC cells must first reach the general circulation and then infiltrate the lung parenchyma. It has been reported that this process requires active killing of lung capillary cells in a mechanism that involves the hormone PTHLH (Urosevic et al., 2014) and possibly necroptosis (Strilic et al., 2016). The capacity of disseminated CRC cells to infiltrate other organs such as the brain is less well characterized and may involve co‐option of invasion mechanisms described for other tumour types such as breast cancer (Valiente et al., 2014).
Work in experimental models has shown that the rate‐limiting step in the metastasis process is the capacity of circulating tumour cells to colonize the foreign organ (Massague and Obenauf, 2016; Obenauf and Massagué, 2015). Most tumour cells that survive in circulation and manage to infiltrate a distant organ will die for reasons that remain incompletely understood but that may include recognition and killing of tumour cells by the innate and adaptive immune system (Collignon et al., 2004; Strauss and Thomas, 2010). Those tumour cells that survive and adapt to the new environment can generate an overt metastasis (Fig. 1). However, not all venturing cancer cells that have successfully pervaded a distant site necessarily have the competency to establish a thriving colony in these hostile environments. Frequently, they remain latent for months to years before resuming growth (Sosa et al., 2014). Below we discuss tumour cell‐intrinsic and cell‐extrinsic aspects that facilitate metastatic colonization in CRC.
Colorectal cancer stem cells and their role in metastasis
Besides (genetic) diversity between patients, no individual CRC is a uniform, clonal mass of cancer cells: any given tumour consists of multiple cell populations with varying levels of phenotypic and genetic heterogeneity. Intratumoral heterogeneity (ITH) is a central concept to understand the phenomena of metastatic progression and therapeutic resistance. Three factors contribute to ITH: the hierarchical organization of cell lineages (Sections 3.1 to 3.3), their clonal diversification (Section 3.4) and the microenvironment (Section 4).
Hierarchical organization of cancer cells
More than 30 years ago, it was already proposed that the phenotypic diversity in cancers could arise from spontaneous differentiation of tumour cells (Pierce and Speers, 1988). The concept, originally developed by G. Barry Pierce in the 1970s, states: ‘[carcinomas] are composed of a mixture of malignant stem cells, which have a marked capacity for proliferation and a limited capacity for differentiation under normal homeostatic conditions, and of the differentiated, possibly benign, progeny of these malignant cells’ (Pierce and Speers, 1988). This hypothesis was long ignored, yet several laboratories have recently put forward evidence to support that CRC complies with this concept. Of note are studies by the groups of Ruggero de Maria (Ricci‐Vitiani et al., 2007), John Dick (O'Brien et al., 2007) and Michael Clarke (Dalerba et al., 2007), wherein each identified a population of tumour cells within human CRCs that has the rare capacity to propagate the disease upon inoculation into immunodeficient mice. Relaunching the idea that CRCs are organized through a hierarchy of cells with distinct tumorigenic potential, they named this population ‘tumour‐initiating cells’.
Subsequent investigation showed that tumour‐initiating cells (also referred to as CRC stem cells or CRC‐SCs) reside at the apex of a hierarchy of tumour cells. They self‐renew, display long‐term proliferation potential and are capable of initiating tumours when inoculated into mice. CRC‐SCs cells express a gene programme that to some extent overlaps with that of normal ISCs, and their progeny can undergo differentiation towards a phenotype similar to that of the normal mucosa. Differentiation coincides with loss of tumorigenic potential (Dalerba et al., 2011; Kreso et al., 2014; Merlos‐Suarez et al., 2011; Vermeulen et al., 2008, 2010). Furthermore, the existence of stem cell hierarchy in CRC has been backed by lineage tracing studies in adenomas (Kozar et al., 2013; Schepers et al., 2012) and by studies of fate‐mapping analysis using lentiviral marking of individual tumour cells (Dieter et al., 2011; Kreso et al., 2012).
The balance between stemness and differentiation in CRC depends upon the same pathways that regulate normal ISCs, including WNT (Vermeulen et al., 2010), BMP (Lombardo et al., 2011) and NOTCH (Lu et al., 2013) signalling. Many of these signals are provided by cells of the tumour stroma, a finding that somewhat contradicts the hypothesis that CRC progresses through gain of ISC niche independency by acquired mutations. Yet, it is worth considering that not every CRC carries alterations in all four driver pathways (WNT, EGFR, TGF‐beta/BMP and p53) and thus may still depend on stromal factors for further progression. As is discussed below, additional stromal‐derived cytokines and growth factors present at the sites of invasion can further promote self‐renewal of CRC‐SCs.
Tumour cell phenotypes at the invasion front
Because CRC‐SCs have both self‐renewal and tumour‐initiating capacity, they likely represent (or give rise to) the so‐called metastatic stem cells (Met‐SCs; Fig. 1), that is the cell of origin of metastasis (Oskarsson et al., 2014). Experimental evidence supports this hypothesis: the above‐mentioned study by the group of Hanno Glimm (Dieter et al., 2011) demonstrates that only cells that hold long‐term self‐renewing ability are capable of generating metastasis.
Most CRCs are a relatively disorganized mixture of stem‐ and differentiated‐like cells that reside into glandular structures reminiscent of the normal crypts (Merlos‐Suarez et al., 2011). Metastases often have an equivalent appearance (Merlos‐Suarez et al., 2011). However, whereas CRC‐SCs present in tumour glands are tumorigenic if isolated and xenografted into mice, naturally they will only be competent to generate metastasis if they first acquire phenotypic changes that enable their migration and extravasation. This process is thought to occur when cancer cells engage in communication with the adjacent tissues and the tumour stroma. A key example is the interaction with endothelial cells, which induce NOTCH signalling on cancer cells to facilitate transendothelial migration via the kinase ABL and RHO activity at invasion fronts (Sonoshita et al., 2011, 2015) (Fig. 2).
In the interest of defining Met‐SCs, there is a long‐standing focus on cancer cells at invasion fronts. A frequent finding in CRCs is the presence of tumour buds – small clusters of detached cancer cells at the invasive border. These budding cells typically possess attributes that help explain their invasive and migratory phenotype, including increased expression of genes involved in extracellular matrix degradation and in epithelial–mesenchymal transition (EMT) (Zlobec et al., 2010). Moreover, cancer cells present at invasion fronts and in tumour buds display increased accumulation of nuclear beta‐catenin (Brabletz et al., 1998), possibly marking stemness. Although most CRCs carry mutations that activate the WNT pathway constitutively, a number of signalling molecules emanating from stromal cells such as HGF (Vermeulen et al., 2010) and PGE2 (Li et al., 2012) have been shown to further elevate WNT signalling in adjacent areas (Fig. 2). In contrast, high levels of nuclear beta‐catenin at invasion fronts do not always correlate with tumour budding and various stem cell markers have been found in only a small fraction of budding cells, casting some doubt on their general representation of Met‐SCs (reviewed in Dawson and Lugli, 2015). Notwithstanding these caveats, tumour budding has consistently been linked to poor survival and is a prognostic factor poised to refine standard clinical risk assessment of early‐stage CRC (van Wyk et al., 2015).
Additional factors derived from the tumour microenvironment that help sustain invasiveness and self‐renewal of CRC‐SCs include IL‐22, expressed by a subset of T cells (Kryczek et al., 2014), and fibroblast‐derived IL‐17A (Lotti et al., 2013). Perhaps the best example connecting invasion and stemness in CRC is the work by Giorgio Stassi, de Maria and colleagues, who found that a subpopulation of CRC‐SCs expressing the surface marker CD44‐v6 is present at invasion fronts and gives rise to metastatic lesions in experimental models (Todaro et al., 2014). CD44‐v6 is required for cell migration, and its expression is increased by factors secreted by stromal cells such as HGF, OPN and SDF‐1 (Todaro et al., 2014). Together with the above‐mentioned WNT‐stimulating mechanisms, these data imply that the microenvironment instructs the formation of migratory CRC‐SCs, or putative Met‐SCs (Fig. 2).
Following local invasion, CRC cells that enter the vasculature are termed circulating tumour cells (CTCs). From a theoretical perspective, both CRC‐SCs and non‐SCs may be able to enter the circulation. Yet, few studies have assessed the heterogeneity of CTCs in regard to their stem cell properties, such as CD133 expression (Iinuma et al., 2011). Still, CTCs have attracted considerable attention for their diagnostic potential, although many challenges – including heterogeneity – impede their robust detection and thus exploitation (reviewed in Hardingham et al., 2015). In contrast, analysing mutations in circulating tumour DNA (ctDNA) appears to be a more straightforward and robust method to detect residual disease and thus to assess risk of relapse after therapy in patients with localized disease (Tie et al., 2016).
Slow‐proliferating and dormant tumour cells
As described in the introductory section, metastasis often develops after a period of latency, which in CRC typically ranges up to 5 years. Latency is the consequence of disseminated cells remaining in a dormant state at distant sites. The current therapeutic strategy to eliminate these residual cells is treatment with standard chemotherapy, which has a limited benefit for the patients. Indeed, dormant and slow‐proliferating cells are largely resistant to chemotherapy, as this typically targets rapidly proliferating cells. In addition, dormant cells remain in a particular state of resilience against cell death‐inducing signals and may even be protected against attacks of the immune system (Ghajar, 2015; Malladi et al., 2016; Massague and Obenauf, 2016). Metastatic latency likely includes two distinct mechanisms: population dormancy, a condition in which tumour cell proliferation and death are balanced, thus leading to micrometastatic lesions that do not expand; or a state of cellular quiescence or temporary mitotic arrest (Ghajar, 2015; Massague and Obenauf, 2016).
The characterization of these mechanisms is of key importance, as a better understanding offers opportunities to cure patients by eliminating the residual disease (or preventing its outgrowth) before appearance of overt metastasis. Although progress in this area has been made for other cancer types (for excellent reviews on this topic, see Ghajar, 2015; Massague and Obenauf, 2016), these processes remain poorly elucidated in CRC. Concerning the latter mechanism, fate‐mapping experiments with xenografts support the existence of slow‐proliferating cells in the tumour bulk. Specifically, not all tumour‐initiating cells responsible for secondary and tertiary transplants had detectably contributed to primary xenografts, implying the existence of dormant cells that can reactivate in tumour re‐initiation (Dieter et al., 2011). Through a similar strategy, such dormant or minor clones were found to gain predominance upon chemotherapy treatment (Kreso et al., 2012).
Whereas the origin, identity and regulation of dormant cell populations in CRCs remain unclear, advances in the understanding of cellular diversity of the normal intestinal epithelium may provide some clues. In the crypts, most cells positive for ISC marker Lgr5 proliferate at high rates and are therefore sensitive to treatment with radio‐ and chemotherapy (Metcalfe et al., 2014; Yan et al., 2012). Douglas Winton and colleagues showed that a subset of Lgr5+ cells that are differentiating towards secretory lineages have slow proliferation kinetics and are relatively chemoresistant (Buczacki et al., 2013). Although these cells are not clonogenic in homoeostasis, they regain stemness and contribute to regenerating the epithelium after ISC pool depletion by treatment with cytostatic drugs. Likewise, lineage tracing experiments in similar settings have shown that differentiated cells of the absorptive and secretory lineage can undergo a process of dedifferentiation and repopulate the ISC niche, gaining self‐renewal capacity (van Es et al., 2012; Tetteh et al., 2015, 2016). Thus, differentiated cells constitute a reservoir of facultative stem cells in normal mucosa. Given the other parallels with CRC, such as cellular hierarchy, it would be clinically relevant to test whether these concepts of (population) dormancy and plasticity also apply to cancer and metastasis. For example, do latent metastatic cells share characteristics – other than chemoresistance – with quiescent crypt cells? And does dedifferentiation facilitate CRC recurrence after treatment?
Linking clonal diversity to cancer stem cell architecture
As a result of genomic instability, cancers acquire hundreds of genetic and epigenetic alterations that impose distinct phenotypes and fates on tumour cells, potentially leading to clonal expansion. This evolutionary phenomenon is the basis for the striking capacity of cancer to adapt to different environments, colonize foreign organs and resist therapy (Boland and Goel, 2005; Nowell, 1976; Swanton, 2012). In CRC, a Big Bang‐like model has been proposed in which tumours go through extensive clonal diversification at early stages, with little indication for stringent selection or clonal expansion. Additionally, malignant behaviour appears to be determined early, and can be inferred from analysing subclone intermixing events (Sottoriva et al., 2015). From this initial genetic diversity, artificial selection pressure in the form of chemotherapy might select for the rise of pre‐existing resistant clones (reviewed in Greaves and Maley, 2012). For instance, minor populations of KRAS mutant cells already present in the primary CRC will expand upon anti‐EGFR therapy, leading to resistant relapses (Diaz et al., 2012).
At the conceptual level, the phenotypic heterogeneity resulting from tumour cell hierarchy and clonal diversity is not necessarily independent. CRC‐SCs likely represent the unit of clonal selection, as mutations occurring in more differentiated cells may have a lower chance of being selected given the relatively short life span of this population (reviewed in Greaves and Maley, 2012; Kreso and Dick, 2014; Valent et al., 2012). A particularly interesting aspect that has been seldom explored is how the genotype affects cellular hierarchy. The WNT (Vermeulen et al., 2010), PI3K (Tenbaum et al., 2012), BMP/TGF‐beta (Lombardo et al., 2011) signalling pathways all affect self‐renewal and differentiation capacity of CRC stem cells, and thus, mutations in these pathways likely regulate the frequency of CRC‐SCs. It is thus possible that successive accumulation of genetic alterations in these pathways increases frequencies of CRC‐SCs, progressively increasing the probability of mutation being selected and thus accelerating evolution, up to a point where full compound mutant tumours contain abundant, variegated populations of CRC‐SCs with limited capacity to produce differentiated progeny. Testing this hypothesis will require analysing how the tumour hierarchy changes in distinct mutational backgrounds.
Although clonal diversity has been linked to therapeutic resistance, somatic evolution and increased metastatic competency, sequencing of primary CRC and metastases has revealed no specific genetic alterations associated with tumour dissemination per se (Jones et al., 2008; Mlecnik et al., 2016b). While equivalent studies analysing epigenetic marks have not been performed, the similarities between primary tumour and metastasis suggest that nongenetic factors might be of particular relevance in this process.
The microenvironment during progression to metastasis
Heterogeneity between patients and within the CRC epithelial compartment already raises significant challenges and opportunities for patient diagnosis and treatment. Yet, further augmenting the complexity, ITH also includes the numerous additional cell types that permeate the tumour and are collectively referred to as stroma or tumour microenvironment (TME). Stromal‐associated functions are linked to all steps of cancer progression and metastasis, and a picture has emerged in which cancer cells and the stroma cross‐communicate and co‐evolve during cancer progression (Hanahan and Coussens, 2012; Quail and Joyce, 2013). Conceptually, transformed cancer cells strongly change the nature and composition of the stroma, to the point that this altered microenvironment forms an adapted niche, providing protection and stimulation, essentially fostering cancer stem cells (Fig. 3).
With the emergence of the TME as a critical player in cancer progression, an increasing effort goes into the characterization of specific stromal cell populations that are held responsible for tumour malignization and metastatic colonization. Several mechanisms have issued from this endeavour, providing potential targets for the design of new anticancer therapies.
Cancer‐associated fibroblasts
Cancer‐associated fibroblasts (CAFs) are a heterogeneous group of fibroblasts that are redirected towards tumour promotion. As in other cancer types, CRC‐associated fibroblasts differ from neighbouring normal fibroblasts and express specific markers including alpha‐smooth muscle actin (alpha‐SMA), fibroblast surface protein (FSP‐1) and fibroblast‐activated protein (FAP) (reviewed in Calon et al., 2014). CAFs provide CRC cells with an array of cytokines that promote cancer cell survival and tumour initiation (Kalluri, 2016). Mechanistically, co‐inoculated CAFs enhance in vivo tumour growth of cancer cells more than normal colon fibroblasts, and soluble factors secreted by the former increase self‐renewal and migration of epithelial cancer cells to a greater extent than those secreted by the latter (Berdiel‐Acer et al., 2014). In addition, gene expression signatures derived from CAFs correlate with poor outcome in colorectal cancer (Becht et al., 2016; Calon et al., 2015; Herrera et al., 2013; Isella et al., 2015). Thus, CAFs constitute an important cell population in the TME and provide a permissive niche for cancer progression (Figs 2 and 3).
TGF‐beta has been linked to poor prognosis in CRC as an independent biomarker across AJCC (American Joint Committee on Cancer) stages, and ligand expression levels correlate with TGF‐beta‐activated stromal cells that secrete a cocktail of additional pro‐metastatic factors (Calon et al., 2012) (Fig. 3). Although TGF‐beta activates a wide range of tumour stroma cell types (Pickup et al., 2013), CAFs are the main contributors to the association of stromal TGF‐beta‐driven programmes with poor clinical outcome in CRC, suggesting a predominant role of TGF‐beta‐activated CAFs during progression to metastasis (Calon et al., 2015). These activated CAFs express several known pro‐metastatic secreted factors including angiopoietin‐like‐4 (ANGPTL‐4) (Padua et al., 2008), connective tissue growth factor (CTGF) (Kang et al., 2003), tenascin C (TNC) (Oskarsson et al., 2011) – functionally described in breast cancer – and periostin (POSTN), a promoter of metastatic growth in colon cancer that increases cell survival via the AKT pathway (Bao et al., 2004). In addition to these factors, we found that TGF‐beta‐activated CAFs secrete interleukin‐11 (IL‐11), which leads to enhanced STAT‐3‐dependent survival and initiation of metastatic cancer cells (Calon et al., 2012). To support the role of this cytokine in CRC progression, an IL‐11 antagonist was shown to reduce both proliferation and invasive capacity of CRC cells (Putoczki et al., 2013). A recent study described an additional function for TGF‐beta in promoting liver metastasis by the adhesion of cancer cells to CAFs, followed by their subsequent codissemination to the metastatic site (Gonzalez‐Zubeldia et al., 2015).
Besides the above‐mentioned TGF‐beta targets, also modifiers of TGF‐beta signalling may be therapeutically relevant in the context of CAFs and liver metastasis. Under physiological condition, hepatic stellate cells (HSCs) are maintained unresponsive to TGF‐beta through degradation of TGF‐beta receptor type‐2, by a process involving IQGAP1 (IQ motif‐containing GTPase‐activating protein). During cancer progression, paracrine signalling emanating from cancer cells decreases IQGAP1 expression in HSCs, which promotes HSC activation into myofibroblasts as well as metastatic outgrowth (Liu et al., 2013). These data indicate that CRC‐SCs are capable of initiating the formation of a metastatic niche by reprogramming resident mesenchymal cells into CAFs. Furthermore, TGF‐beta signalling in HSCs was shown to be modulated by platelet‐derived growth factor receptor (PDGFR)‐alpha, leading to paracrine effects on CRC cell proliferation and migration (Liu et al., 2014). This adds to the rationale for the inhibition of the PDGFR signalling pathway with imatinib, a compound targeting tyrosine kinases including PDGFRs. This drug was previously proposed as a therapeutic agent in CRC for its effects on impairing migration of bone marrow‐derived mesenchymal stem cells (MSCs) to the tumour site, resulting in decreased metastatic intake (Shinagawa et al., 2013). Incidentally, MSCs have also been reported to be differentiated into CAF‐like cells in the TME (Shinagawa et al., 2010).
Endothelial cells
The stromal niche surrounding cancer cells comprises a constantly developing network of blood vessels, supplying the growing tumour with oxygen and nutrients. Secreted factors produced in the tumour stimulate proliferation and survival of endothelial cells, thus enhancing angiogenesis. Tumour‐associated angiogenesis gives rise to abnormal blood vessels characterized by a chaotic network, excessive branching, decreased pericyte coverage and leakiness (Dudley, 2012). The latter has been associated with metastasis and poor prognosis in patients with CRC (Yonenaga et al., 2005).
VEGFA is a key regulator of endothelial cell proliferation in most human tumours, inducing the MAPK/ERK signalling pathway. Tumoral VEGFA expression correlates with invasiveness, increased vascular density and progression to metastasis. Accordingly, bevacizumab, a monoclonal antibody against VEGFA and an inhibitor of angiogenesis, has been shown to increase survival of patients with stage IV CRC when combined with chemotherapy (Ferrara and Adamis, 2016; Hurwitz et al., 2004; Mathonnet, 2014) (Figs 2 and 3). Besides blocking neo‐angiogenesis, the clinical benefit of a dual‐targeting approach may involve the reprogramming of tumour‐associated blood vessels into normalized blood vessels by bevacizumab, decreasing vessel permeability and improving anticancer drug bioavailability into the tumour mass (Jain, 2005).
Interleukin‐33 (IL‐33), a cytokine secreted by endothelial and epithelial cells to activate NF‐κB and MAPK signalling, may also hold therapeutic interest for the reprogramming of endothelial cells and normalization of tumour vasculature in CRC. Tumour‐derived IL‐33 dramatically enhances neo‐angiogenesis by increasing endothelial cell proliferation, migration and differentiation into blood vessels to robustly increase metastatic spreading of CRC cells to the liver (Zhang et al., 2016). Conversely, blockade of IL‐33 signalling suppresses angiogenesis and reduces tumorigenesis (Maywald et al., 2015).
Endothelial cells are a part of perivascular niches that have been reported to foster cancer stem cells (Butler et al., 2010). A mechanism in which endothelial cells directly promote the formation of CRC‐SCs involves a soluble form of Jagged‐1 to activate NOTCH signalling in cancer cells (Lu et al., 2013) (Fig. 2). Another way in which endothelial cells might participate more directly in niche formation is their conversion into CAF‐like cells, through a TGF‐beta‐driven mechanism called endothelial–mesenchymal transition (EndMT). This process is associated with the upregulation of fibroblast‐specific protein‐1 (FSP‐1) and downregulation of the endothelial marker CD31 (Zeisberg et al., 2007). Although the existence of EndMT in CRC remains elusive, a similar mechanism was reported in response to inflammation in the colon (Rieder et al., 2011).
Immune cells
As the immune system can be a powerful weapon against tumorigenesis through coordinated elimination of aberrant cells, successful cancers find a way to circumvent tumour immunity; this is recognized as a hallmark of cancer (Hanahan and Weinberg, 2011). In fact, it has become increasingly clear that the immune system has a dual role in cancer, able to both suppress and promote cancer progression (Schreiber et al., 2011). Even if a thriving cancer suggests inhibition of the former and exploitation of the latter, there is evidence for a continued battle between the immune system and cancer cells. First, there is a positive prognostic value of the presence of infiltrating immune cells such as T cells (Galon et al., 2006) and dendritic cells (Gulubova et al., 2012), as well as high levels of gene signatures of active immune responses (Galon et al., 2006). Conversely, the presence in blood and tumour of immunosuppressive myeloid‐derived suppressor cells (MDSCs) (Solito et al., 2011; Sun et al., 2012) correlates with a poor prognosis. Second, cancers show signs of immunoselection, where the number of neoantigens is lower than expected based on mutation rates. This can be caused by T cell‐mediated killing of cells or clones expressing immunogenic neoantigens (Matsushita et al., 2012) or by loss of antigen expression or presentation (DuPage et al., 2012; Rooney et al., 2015).
Together, this indicates that evasion from antitumour immunity is only partial, local or reversible and that immunity is likely a key hurdle to overcome in the metastatic process. Relatedly, metastatic latency and population dormancy have been linked to immunosurveillance in a melanoma model, where (micro)metastasis growth was equilibrated by immunologic cancer cell killing (Eyles et al., 2010) (reviewed in Giancotti, 2013; Sosa et al., 2014). Although many of these important concepts are emerging for cancer in general (Vinay et al., 2015), less is known about the specific situation in CRC. Nevertheless, below are some recently described mechanisms that together have an important impact on the prospects of immunotherapies.
Innate immune cells
Besides their role in innate immunity and the coordination of adaptive immune responses, several bone marrow‐derived myeloid cells have been linked to tumour progression (Taketo, 2009). Chemokine signalling may play an important role in their recruitment and subsequent communication with CRC cells and other TME residents, often promoting both cancer progression and metastasis (Itatani et al., 2016) (Fig. 3). Immature myeloid cells positive for C‐C chemokine receptor type 1 (CCR1) have been linked to CRC progression and liver metastasis (Kitamura et al., 2007, 2010), in a mechanism that involves the loss of SMAD4 in CRC cells, triggering CCL15‐mediated recruitment of CCR1+ myeloid cells (Hirai et al., 2014; Itatani et al., 2013). Similar mechanisms link MDSCs to CRC progression through the action of CCL15 (Inamoto et al., 2016) or CCL2 (Chun et al., 2015).
Macrophages, one of the most abundant tumour‐infiltrating cell types, have been ascribed many tumour suppressor roles in CRC, ranging from direct cytotoxicity to orchestrating and sustaining adaptive responses (Braster et al., 2015). Besides this classical functional state (often called M1), alternative activation states such as M2 (also referred to as tumour‐associated macrophages or TAMs) have been described; these are characterized by mostly pro‐tumorigenic potential (reviewed in Mantovani et al., 2009). Polarization of macrophages is incompletely understood but appears to be plastic and largely dependent on the TME (reviewed in Braster et al., 2015). Recently, much attention has gone towards the clinical implication of the presence, plasticity and dual functions of TAMs (Braster et al., 2015; Mantovani and Allavena, 2015). For example, their accumulation at the liver metastatic periphery was recently shown to lend itself for exploitation, when a gene transfer strategy delivered interferon‐alpha to the TME via Tie2+ monocytes/macrophages in a mouse model for CRC metastasis, resulting in reduced tumour growth and enhanced survival (Catarinella et al., 2016) (Fig. 3).
Like macrophages, neutrophils (a class of granulocytes) have been found to undergo functional repolarization in the TME, a process that involves TGF‐beta (Fridlender et al., 2009) and converts them into a pro‐tumorigenic state (N2 vs. N1). Tumour‐associated neutrophils (TANs), like MDSCs, can be recruited to SMAD4‐mutant metastatic cancer cells by CCL15 and help promote lung colonization (Yamamoto et al., 2016). In addition, a recent report links neutrophils to cancer recurrence after surgery through a defence mechanism involving the release of neutrophil chromatin strands: neutrophil extracellular traps (Tohme et al., 2016). These may be possible explanations for the emergence of a high neutrophil‐to‐lymphocyte ratio as a potential poor‐prognosis marker for patients with CRC (Li et al., 2014).
Adaptive immune cells
Specialized, adaptive immune responses heavily rely on cells from the lymphoid lineage, including T cells and B cells. Central mediators of adaptive responses are CD8+ cytotoxic T lymphocytes (CTLs) that recognize specific antigens. For their function, they require assistance and reinforcement from CD4+ T‐helper cells as well as from myeloid cells. CTL infiltration in CRC is a factor for good prognosis, and lack thereof indicates poor disease outcome (Galon et al., 2006; Naito et al., 1998; Ropponen et al., 1997), indicating that T cell‐mediated immune surveillance plays an important role in CRC metastasis. Therefore, microsatellite‐instable (MSI) cancers, bearing multiple mutations that can translate into aberrant (peptide) antigens, may be linked to good prognosis – in large measure – because of effective adaptive immune responses (Kloor and von Knebel Doeberitz, 2016; Rooney et al., 2015).
A growing number of recent therapeutic strategies aim to enhance existing T‐cell responses, and early results point to successes mainly in MSI cancers (see Section 5.4). Besides reprogramming neutrophils, TGF‐beta has been shown to repolarize various other immune cell types, including natural killer cells, dendritic cells, macrophages and T cells (Flavell et al., 2010), and to directly inhibit T‐cell mechanisms (Chen et al., 2005; Thomas and Massague, 2005; Yang et al., 2010; Zhang et al., 2005). Moreover, dendritic cells, MDSCs and tumour‐associated macrophages are all, like CAFs, sources for stromal TGF‐beta (Gabrilovich and Nagaraj, 2009), indicating a mechanism in which TGF‐beta reprogrammes a variety of stromal cells, amplifying its own signal, and impeding anticancer immune responses in a concerted way.
Heterogeneity of the TME as a tool to stratify patients with CRC
As described above, an understanding of the extent of intra‐ and intertumour variegation helps frame the limited accuracy of the generic AJCC staging system in predicting disease outcome, and has provided a number of additional parameters for prognostic use. Numerous findings underscore the prognostic value of immune cells in the tumour stroma during cancer progression. As mentioned above, the work by Jérôme Galon and colleagues showed that an index evaluating the type and localization of immune cells (Immunoscore) can predict disease outcome. Indeed, they demonstrated a stronger prognostic power than the classical TNM (tumour, lymph node, metastasis) system (Galon et al., 2006, 2014; Mlecnik et al., 2016a,b).
Furthermore, since the development of DNA microarray technology, there has been a growing interest in refining CRC patient stratification with unbiased molecular classification based on gene expression profiles (Blanco‐Calvo et al., 2015; Golub et al., 1999). A series of recent studies have identified between three and six molecular subtypes of CRCs associated with distinct outcome and response to treatment (Budinska et al., 2013; De Sousa E Melo et al., 2013; Marisa et al., 2013; Roepman et al., 2014; Sadanandam et al., 2013; Schlicker et al., 2012). To consolidate the various classifiers, a consortium of experts in the field of molecular classification integrated these molecular stratifications of CRC into four consensus molecular subtypes (CMS) (Guinney et al., 2015). CMS1 includes most of the MSI and CpG island methylator phenotype (CIMP)‐high CRCs, whereas CMS2, CMS3 and CMS4 are generally chromosome‐instable tumours displaying roughly equivalent genotypes yet distinct expression profiles. CRCs belonging to CMS2 express a gene programme that suggests elevated WNT/MYC activation, and thus, they may represent the canonical class of CRC. CMS3 cancers express signatures that reflect particular metabolic reprogramming, and those of CMS4 display elevated expression of mesenchymal genes.
Importantly, CMS4 is associated with poor outcome. Whereas mesenchymal gene expression was initially attributed to cancer cells undergoing EMT, two studies revealed that the signatures that identified patients with the worst outcome were in fact of stromal origin (Calon et al., 2015; Isella et al., 2015). Recent analysis also suggests that the gene expression profile of the CMS4 subtype reflects immunosuppression (Becht et al., 2016). Importantly, the power of stromal gene signatures to predict disease relapse outperforms both the classical AJCC staging system and the consensus molecular stratification of patients (Calon et al., 2015; Isella et al., 2015). As mentioned in earlier sections, further investigation within these prognostic stromal gene signatures identified a prominence of TGF‐beta target genes expressed by CAFs in the most aggressive tumours, which are promising poor‐prognosis biomarkers that can be assessed using either transcriptomic or immunohistochemical techniques (Calon et al., 2012, 2015). Altogether, these data suggest that stromal evaluation will greatly benefit upcoming patient classification systems and may translate to better clinical assessment of the disease, while also providing new avenues for therapeutic intervention.
Specific targeting of cell types to treat metastasis
For many years, the standard of care for advanced disease had been 5‐fluorouracil – commonly supplemented with folinic acid – which only conferred a marginal survival advantage. Somewhat more encouraging results emerged from the addition of oxaliplatin or irinotecan to the regimen (FOLFOX or FOLFIRI, respectively) both in metastatic disease (Douillard et al., 2000; de Gramont et al., 2000) and, as adjuvant therapy, in some stage II and most stage III CRC patients (André et al., 2009; Van Cutsem et al., 2016). However, these systemic chemotherapies in effect indiscriminately kill proliferative cells and their therapeutic index is limited for many patients. Moreover, this approach neither targets dormant CRC‐SCs nor offers an answer to resistance or stromal mitigation. Understanding intratumoral heterogeneity and the biology of the different cell types that populate the tumour is guiding the development of new therapeutic strategies to treat advanced disease.
Targeted therapies
Standard systemic chemotherapy is increasingly combined with targeted treatments that eliminate specific dysregulated pathways crucial for cancer growth or survival. For example, inhibitors of EGFR signalling such as cetuximab and panitumumab improve survival in patients with CRC (Van Cutsem et al., 2016) (Fig. 3). Unfortunately, these therapies are met with both intrinsic and acquired resistance in the vast majority of cases, often involving mutations downstream to EGFR (including in KRAS and BRAF genes), but also in other mitogenic protein kinase receptor signalling pathways (Bertotti et al., 2015).
As additional targeted therapies become available, the development of increasingly adding cancer genome and transcriptome sequencing to regular clinical practice might help in this systematic approach of targeting signalling networks most relevant to individual tumours. However, clonal diversity can severely complicate this class of analysis (see Section 3.4). Additionally, signalling networks perturbed in one way can rewire elsewhere and confer resistance, indicating a challenge in providing straightforward biomarkers for response for targeted therapies (Prahallad et al., 2012). Therapies combining multiple pathway inhibitors are being tested as a way to prevent resistance to individual drugs, but these strategies may face important toxic effects on normal tissues that limit their implementation.
Therapies against cancer stem cells
The hierarchical organization of CRC has led to the hypothesis that the cause of disease relapse is that standard chemotherapy eliminates the tumour bulk while sparing CRC‐SCs. While formal proof for this idea is still lacking, several initiatives to develop anti‐CRC‐SC therapies are currently ongoing. There are three classes of such therapies. First, targeting the key pathways that regulate the behaviour of CRC‐SCs – including WNT, NOTCH, EGFR and TGF‐beta/BMP – is an obvious approach to prevent the maintenance or expansion of this cell population. Whereas inhibitors and agonist of these pathways exist, they are not always effective, given the fact that CRCs carry genetic alterations that alter many or all of these pathways. For instance, CRC‐SCs depend on WNT signalling to sustain self‐renewal, and inhibitors of WNT secretion and of WNT receptors are in advanced stages of testing. Yet, the vast majority of CRCs carry mutations in the tumour suppressor gene APC, which constitutively activate the pathway downstream of the receptor. Unfortunately, developing inhibitors that target pathway components downstream of APC has proven to be tremendously challenging (Anastas and Moon, 2012; Kahn, 2014), although two recent studies reported promising compounds. The first, called NCB‐0846, inhibits TNIK (an essential regulatory component of WNT/beta‐catenin signalling (Mahmoudi et al., 2009)) and effectively abrogates CRC stemness in vitro and polyp formation in mice (Masuda et al., 2016). The second (called MSAB) binds to beta‐catenin and promotes its proteasomal degradation, inhibiting the growth of xenograft tumours in mice (Hwang et al., 2016) (Fig. 2). A drawback of this class of strategies is the fact that normal ISCs also critically depend on the same pathways as CRC‐SCs, which may lead to strong side effects.
A second therapeutic strategy is to deplete CRC‐SCs through the use of antibodies–drug conjugates (ADCs) designed to bind surface antigens expressed by this cell population. As recently shown, antibodies targeting Lgr5 coupled to different toxins demonstrated potent antitumour efficacy in preclinical models of CRC (Junttila et al., 2015) (Fig. 3). Again, this strategy may also have significant side effects given the fact that many surface makers of CRC‐SCs are shared with normal ISCs. Furthermore, as discussed in Section 3.3, if stress‐induced dedifferentiation in the normal crypt has its parallel in cancer, regeneration of CRC‐SCs pool by conversion of non‐SCs cells upon cessation of the treatment may also limit the effectiveness of this strategy (Fig. 3).
A third strategy relies on identifying molecules and dependencies specific for CRC‐SCs that can be targeted therapeutically, supposedly without major toxicities. For instance, targeting self‐renewal of CRC‐SCs using an inhibitor of BMI1 (PTC‐209) has been shown to have robust therapeutic effects (Kreso et al., 2014). ER‐stress‐induced activation of the unfolded protein response (UPR) forces CRC‐SCs to differentiate, and therefore, drugs that induce UPR could have therapeutic activity against this cell population (Wielenga et al., 2015). Furthermore, a low dose of the DNA‐demethylating agent 5‐AZA‐CdR induces viral‐like response in CRC‐SCs by triggering the expression of double‐stranded RNAs derived from endogenous retroviral elements, which has an antitumoral effect (Roulois et al., 2015) (Fig. 3).
Stromal therapies
In line with the growing realization that a large number of stromal cells are actively involved in driving CRC progression (including maintenance of CRC‐SCs), new strategies are taking shape wherein either the TME is the main target or a combination of agents attacks both cancer cells and stromal cells, to improve therapeutic response and prevent acquired resistance (Fang and Declerck, 2013). For example, a recent study suggested that HGF secreted by fibroblasts might decrease the response to irinotecan. The successful reversion of such resistance using anti‐HGF‐targeted therapy (Woo et al., 2015) emphasizes the promises of multitargeted treatments for patients (Fig. 3). This strategy might also be of high value for CRC patients with nonmutated KRAS gene where resistance to inhibitors of EGFR is associated with increased levels of HGF (Liska et al., 2011; Takahashi et al., 2014).
As mentioned in Section 4.2, another group of widely applied agents for CRC treatment in fact target the TME. These drugs inhibit VEGF signalling in endothelial cells and thereby oppose tumour vascularization. Besides monoclonal antibodies, also a recombinant fusion protein (aflibercept, blocking VEGFA, VEGFB and placental growth factor signalling) was shown to improve survival in phase III trials on selected patients with metastatic CRC (Van Cutsem et al., 2012). However, the majority of responsive patients tend to develop resistance to anti‐angiogenic therapies over time, in part because the hypoxic conditions established during treatment may independently cause further malignization of cancer cells (Ulivi et al., 2016). Nevertheless, anti‐angiogenic therapies are likely to continue to be part of future combinatory treatment strategies.
Instead of targeting elements in the TME for depletion or destruction, an attractive alternative is the repolarization of stromal cells into a nonpermissive state, for instance by blocking or reverting the corruptive signals from cancer cells. In this perspective, stromal reprogramming might have a lower toxicity than destructive therapies and can thus be a powerful tool to combine with more conventional treatments. The many stromal pro‐tumorigenic functions associated with TGF‐beta in CRC (and other cancers) suggest that its successful and safe inhibition would be an invaluable therapeutic goal. In a mouse model of metastatic initiation, stromal TGF‐beta signalling enhanced metastatic spreading, while therapeutic inhibition of this pathway in the stroma with galunisertib abrogated liver metastasis initiation by CRC cells (Calon et al., 2012, 2015) (Fig. 3). Extensive discussion on the implementation of anti‐TGF‐beta therapies for advanced CRC can be found elsewhere (Tauriello and Batlle, 2016).
Immunotherapies
It has been proposed that conventional chemotherapy may in large part rely on immune components to be efficient, for instance by causing immunologic cell death (Zitvogel et al., 2013). Consequently, T‐cell infiltration of both the primary tumour and liver metastases has been associated with response to chemotherapy in patients with metastatic CRC (Halama et al., 2009, 2011). Immunotherapies – which aim to directly induce immune responses, or to enhance pre‐existing ones – have seen impressive efficacies in a growing number of cancer types (Palucka and Coussens, 2016). Designed to activate tumour‐specific CD8+ CTL immune responses, cancer vaccines have demonstrated benefit in prostate cancer, melanoma and other cancer types (Butterfield, 2015), and several strategies have been developed for CRC (Xiang et al., 2013). Many such treatments focussed on advanced (metastatic) disease have had disappointing responses, possibly in part because of the progressively immunosuppressive TMEs of those tumours, suggesting a higher benefit at earlier stages (Merika et al., 2010). Recently, promising results were reported for a vaccine based on a mucin‐1 peptide in prophylactic treatment of patients with precancerous adenomas (Kimura et al., 2013). Even in this study, treatment failure was linked to the presence of high levels of immunosuppressive MDSCs already at this early stage, which might be a useful biomarker for further exploration of similar strategies. Furthermore, these cells can be therapeutic target themselves. To circumvent both the requirement of in situ activation and the problem of tumoral immune tolerance, a passive form of immunotherapy can be used, where in vitro‐activated immune effectors (most often T cells) are administered to the patient. However, early trials with adoptive cell therapy resulted in severe toxicities and were not efficacious (Xiang et al., 2013).
Early clinical trials with a different type of immunotherapy – checkpoint inhibition, which unblocks T cell‐mediated adaptive anticancer responses – have shown benefit in at least a subset of patients with CRC (Puzzoni et al., 2016; Zumwalt and Goel, 2015) (Fig. 3). Notably responsive are hypermutated MSI tumours, which commonly carry many neoantigens, are heavily infiltrated by T lymphocytes and express relatively high levels of various checkpoints (Diaz and Le, 2015; Kloor et al., 2010; Llosa et al., 2015). However, even in microsatellite‐stable CRCs, there is a correlation between mutational/neoantigen load, immune infiltration and survival (Giannakis et al., 2016), offering a perspective on successful future exploitation of immunotherapies. Several clinical trials are ongoing, evaluating the benefit of checkpoint inhibitors such as anti‐CTLA‐4 or anti‐PD‐1 antibodies (Moehler et al., 2016). In addition, combinations of multiple checkpoint inhibitors, or of such agents with other strategies such as vaccines and/or chemotherapy, are likely to increase the number of patients with good responses (Sharma and Allison, 2015).
Alternatively, immunotherapy can be designed to inhibit pro‐tumorigenic interactions between immune cells and neoplastic CRC cells. In a phase I trial, cancer–stromal crosstalk through accumulating myeloid cells and T cells, and pro‐tumorigenic cytokine signalling, was successfully targeted using anti‐CCR5 therapy in patients with advanced/metastatic CRC (Halama et al., 2016) (Fig. 3). As TGF‐beta is a classical immune suppressor as well as a key modulator of cellular crosstalk, the discovery that high levels of TGF‐beta correlate with poor prognosis may imply that colorectal cancer exploits this cytokine in tumoral immune evasion, besides affecting CAF‐mediated secretion of pro‐tumorigenic factors (Tauriello and Batlle, 2016). It will be of great interest to study the effects of this therapeutic strategy in immunocompetent models, as well as explore the putative role of CAFs as immunosuppressors (Feig et al., 2013; Kraman et al., 2010). Indeed, TGF‐beta inhibition, for which several approaches are in clinical trials (Akhurst and Hata, 2012; Neuzillet et al., 2015; Smith et al., 2012), might act as or synergize with immunotherapy.
Concluding remarks
Taken together, recent data discussed here emphasize the importance of tumour heterogeneity – in terms of cellular hierarchy, clonal diversity and tumour microenvironment – in modulating CRC progression and metastasis (Fig. 1). These factors have strong implications for patient stratification as well as for the development, optimization and application of therapeutic strategies (Figs 2 and 3). While key mechanisms and dependencies in cancer progression and metastasis are increasingly being translated into targeted therapies, it is vital to integrate these emerging concepts both in the selection of patients for clinical testing of new agents and in combining approved therapies for the treatment of individual patients.
All types of heterogeneity play a role in generating and maintaining colorectal cancer stem cells (CRC‐SCs) with chemoresistance and metastatic competency, and particularly, the TME supports metastatic colonization (Figs 2 and 3). Therefore, therapies that target any or several of the mechanisms discussed here may potentially be able to prevent metastasis from developing in the 40–50% of patients with early‐stage disease at risk of distant recurrence. Moreover, several of these therapies may be very beneficial for patients with advanced/metastatic CRC. Among these promising therapeutic strategies are treatments that target CRC‐SCs directly or through their dependency on the TME. In addition, a deeper understanding of colorectal cancer immunity may lead to a better exploitation of immunotherapeutic options, as well as offering opportunities in targeting immunosuppressive mechanisms.
The fast pace of progress as well as the high number of open questions in each of the research fields we have borrowed from assures that there will be significant challenges ahead in our understanding of the full complexity of CRC as a heterogeneous disease. Breaking our inability to effectively treat metastasis requires the concerted effort of a large number of researchers and clinicians and will likely involve patient‐specific combination of therapies aimed at targeted elimination of metastatic competency mechanisms.
References 194
- 1.
Akhurst RJ and Hata A (2012 ) Targeting the TGFbeta signalling pathway in disease. Nat Rev Drug Discov 11, 790–811.
Not in our library10.1038/nrd3810
- 2.
Anastas JN and Moon RT (2012 ) WNT signalling pathways as therapeutic targets in cancer. Nat Rev Cancer 13, 11–26.
Not in our library10.1038/nrc3419
- 3.
André T, Boni C, Navarro M, Tabernero J, Hickish T, Topham C, Bonetti A, Clingan P, Bridgewater J, Rivera F et al (2009 ) Improved overall survival with oxaliplatin, fluorouracil, and leucovorin as adjuvant treatment in stage II or III colon cancer in the MOSAIC trial. J Clin Oncol 27, 3109–3116.
Not in our library10.1200/jco.2008.20.6771
- 4.
Bao S, Ouyang G, Bai X, Huang Z, Ma C, Liu M, Shao R, Anderson RM, Rich JN and Wang XF (2004 ) Periostin potently promotes metastatic growth of colon cancer by augmenting cell survival via the Akt/PKB pathway. Cancer Cell 5, 329–339.
Not in our library10.1016/s1535-6108(04)00081-9
- 5.
Barker N, Ridgway RA, van Es JH, van de Wetering M, Begthel H, van den Born M, Danenberg E, Clarke AR, Sansom OJ and Clevers H (2008 ) Crypt stem cells as the cells‐of‐origin of intestinal cancer. Nature 457, 608–611.
Not in our library10.1038/nature07602
- 6.
Becht E, de Reyniès A, Giraldo NA, Pilati C, Buttard B, Lacroix L, Sèlves J, Sautès‐Fridman C, Laurent‐Puig P and Fridman W‐H (2016 ) Immune and stromal classification of colorectal cancer is associated with molecular subtypes and relevant for precision immunotherapy. Clin Cancer Res 22, 4057–4066.
Not in our library10.1158/1078-0432.ccr-15-2879
- 7.
Berdiel‐Acer M, Sanz‐Pamplona R, Calon A, Cuadras D, Berenguer A, Sanjuan X, Paules MJ, Salazar R, Moreno V, Batlle E et al (2014 ) Differences between CAFs and their paired NCF from adjacent colonic mucosa reveal functional heterogeneity of CAFs, providing prognostic information. Mol Oncol 8, 1290–1305.
Not in our library10.1016/j.molonc.2014.04.006
- 8.
Bertotti A, Papp E, Jones S, Adleff V, Anagnostou V, Lupo B, Sausen M, Phallen J, Hruban CA, Tokheim C et al (2015 ) The genomic landscape of response to EGFR blockade in colorectal cancer. Nature 526, 263–267.
Not in our library10.1038/nature14969
- 9.
Bishehsari F, Mahdavinia M, Vacca M, Malekzadeh R and Mariani‐Costantini R (2014 ) Epidemiological transition of colorectal cancer in developing countries: environmental factors, molecular pathways, and opportunities for prevention. World J Gastroenterol 20, 6055–6072.
Not in our library10.3748/wjg.v20.i20.6055
- 10.
Blanco‐Calvo M, Concha Á, Figueroa A, Garrido F and Valladares‐Ayerbes M (2015 ) Colorectal cancer classification and cell heterogeneity: a systems oncology approach. Int J Mol Sci 16, 13610–13632.
Not in our library10.3390/ijms160613610
- 11.
Boland CR and Goel A (2005 ) Somatic evolution of cancer cells. Semin Cancer Biol 15, 436–450.
Not in our library10.1016/j.semcancer.2005.06.001
- 12.
Brabletz T, Jung A, Hermann K, Günther K, Hohenberger W and Kirchner T (1998 ) Nuclear overexpression of the oncoprotein beta‐catenin in colorectal cancer is localized predominantly at the invasion front. Pathol Res Pract 194, 701–704.
Not in our library10.1016/s0344-0338(98)80129-5
- 13.
Braster R, Bögels M, Beelen RHJ and van Egmond M (2015 ) The delicate balance of macrophages in colorectal cancer; their role in tumour development and therapeutic potential. Immunobiology 222, 21–30.
Not in our library10.1016/j.imbio.2015.08.011
- 14.
Buczacki SJA, Zecchini HI, Nicholson AM, Russell R, Vermeulen L, Kemp R and Winton DJ (2013 ) Intestinal label‐retaining cells are secretory precursors expressing Lgr5. Nature 495, 65–69.
Not in our library10.1038/nature11965
- 15.
- 16.
Butler JM, Kobayashi H and Rafii S (2010 ) Instructive role of the vascular niche in promoting tumour growth and tissue repair by angiocrine factors. Nat Rev Cancer 10, 138–146.
Not in our library10.1038/nrc2791
- 17.
Butterfield LH (2015 ) Cancer vaccines. BMJ 350, h988.
Not in our library10.1136/bmj.h988
- 18.
Calon A, Espinet E, Palomo‐Ponce S, Tauriello DVF, Iglesias M, Céspedes MV, Sevillano M, Nadal C, Jung P, Zhang XH‐FF et al (2012 ) Dependency of colorectal cancer on a TGF‐β‐driven program in stromal cells for metastasis initiation. Cancer Cell 22, 571–584.
Not in our library10.1016/j.ccr.2012.08.013
- 19.
Calon A, Lonardo E, Berenguer‐llergo A, Espinet E, Hernando‐momblona X, Iglesias M, Sevillano M, Palomo‐ponce S, Tauriello DVF, Byrom D et al (2015 ) Stromal gene expression defines poor‐prognosis subtypes in colorectal cancer. Nat Genet 47, 320–329.
Not in our library10.1038/ng.3225
- 20.
Calon A, Tauriello DVF and Batlle E (2014 ) TGF‐beta in CAF‐mediated tumor growth and metastasis. Semin Cancer Biol 25, 15–22.
Not in our library10.1016/j.semcancer.2013.12.008
- 21.
Cancer Genome Atlas Network (2012 ) Comprehensive molecular characterization of human colon and rectal cancer. Nature 487, 330–337.
Not in our library10.1038/nature11252
- 22.
Catarinella M, Monestiroli A, Escobar G, Fiocchi A, Tran NL, Aiolfi R, Marra P, Esposito A, Cipriani F, Aldrighetti L et al (2016 ) IFNα gene/cell therapy curbs colorectal cancer colonization of the liver by acting on the hepatic microenvironment. EMBO Mol Med 8, 155–170.
Not in our library10.15252/emmm.201505395
- 23.
Chen ML, Pittet MJ, Gorelik L, Flavell RA, Weissleder R, von Boehmer H and Khazaie K (2005 ) Regulatory T cells suppress tumor‐specific CD8 T cell cytotoxicity through TGF‐beta signals in vivo. Proc Natl Acad Sci USA 102, 419–424.
Not in our library10.1073/pnas.0408197102
- 24.
Chun E, Lavoie S, Michaud M, Gallini CA, Kim J, Soucy G, Odze R, Glickman JN and Garrett WS (2015 ) CCL2 promotes colorectal carcinogenesis by enhancing polymorphonuclear myeloid‐derived suppressor cell population and function. Cell Rep 12, 244–257.
Not in our library10.1016/j.celrep.2015.06.024
- 25.
Clevers H (2013 ) The intestinal crypt, a prototype stem cell compartment. Cell 154, 274–284.
Not in our library10.1016/j.cell.2013.07.004
- 26.
Collignon FP, Holland EC and Feng S (2004 ) Organ donors with malignant gliomas: an update. Am J Transplant 4, 15–21.
Not in our library10.1046/j.1600-6143.2003.00289.x
- 27.
Dalerba P, Dylla SJ, Park I‐K, Liu R, Wang X, Cho RW, Hoey T, Gurney A, Huang EH, Simeone DM et al (2007 ) Phenotypic characterization of human colorectal cancer stem cells. Proc Natl Acad Sci USA 104, 10158–10163.
Not in our library10.1073/pnas.0703478104
- 28.
Dalerba P, Kalisky T, Sahoo D, Rajendran PS, Rothenberg ME, Leyrat AA, Sim S, Okamoto J, Johnston DM, Qian D et al (2011 ) Single‐cell dissection of transcriptional heterogeneity in human colon tumors. Nat Biotechnol 29, 1120–1127.
Not in our library10.1038/nbt.2038
- 29.
Davis H, Irshad S, Bansal M, Rafferty H, Boitsova T, Bardella C, Jaeger E, Lewis A, Freeman‐Mills L, Giner FC et al (2014 ) Aberrant epithelial GREM1 expression initiates colonic tumorigenesis from cells outside the stem cell niche. Nat Med 21, 62–70.
Not in our library10.1038/nm.3750
- 30.
Dawson H and Lugli A (2015 ) Molecular and pathogenetic aspects of tumor budding in colorectal cancer. Front Med (Lausanne) 2, 11.
Not in our library10.3389/fmed.2015.00011
- 31.
de Gramont A, Figer A, Seymour M, Homerin M, Hmissi A, Cassidy J, Boni C, Cortes‐Funes H, Cervantes A, Freyer G et al (2000 ) Leucovorin and fluorouracil with or without oxaliplatin as first‐line treatment in advanced colorectal cancer. J Clin Oncol 18, 2938–2947.
Not in our library10.1200/jco.2000.18.16.2938
- 32.
De Sousa E Melo F, Wang X, Jansen M, Fessler E, Trinh A, de Rooij LPMH, de Jong JH, de Boer OJ, van Leersum R, Bijlsma MF et al (2013 ) Poor‐prognosis colon cancer is defined by a molecularly distinct subtype and develops from serrated precursor lesions. Nat Med 19, 614–618.
Not in our library10.1038/nm.3174
- 33.
Diaz LA Jr and Le DT (2015 ) PD‐1 blockade in tumors with mismatch‐repair deficiency. N Engl J Med 373, 1979.
Not in our library10.1056/nejmc1510353
- 34.
Diaz LA Jr, Williams RT, Wu J, Kinde I, Hecht JR, Berlin J, Allen B, Bozic I, Reiter JG, Nowak MA et al (2012 ) The molecular evolution of acquired resistance to targeted EGFR blockade in colorectal cancers. Nature 486, 537.
Not in our library10.1038/nature11219
- 35.
Dieter SM, Ball CR, Hoffmann CM, Nowrouzi A, Herbst F, Zavidij O, Abel U, Arens A, Weichert W, Brand K et al (2011 ) Distinct types of tumor‐initiating cells form human colon cancer tumors and metastases. Cell Stem Cell 9, 357–365.
Not in our library10.1016/j.stem.2011.08.010
- 36.
Douillard J, Cunningham D, Roth A, Navarro M, James R, Karasek P, Jandik P, Iveson T, Carmichael J, Alakl M et al (2000 ) Irinotecan combined with fluorouracil compared with fluorouracil alone as first‐line treatment for metastatic colorectal cancer: a multicentre randomised trial. Lancet 355, 1041–1047.
Not in our library10.1016/s0140-6736(00)02034-1
- 37.
Drost J, van Jaarsveld RH, Ponsioen B, Zimberlin C, van Boxtel R, Buijs A, Sachs N, Overmeer RM, Offerhaus GJ, Begthel H et al (2015 ) Sequential cancer mutations in cultured human intestinal stem cells. Nature 521, 43–47.
Not in our library10.1038/nature14415
- 38.
Dudley AC (2012 ) Tumor endothelial cells. Cold Spring Harb Perspect Med 2, a006536.
Not in our library10.1101/cshperspect.a006536
- 39.
DuPage M, Mazumdar C, Schmidt LM, Cheung AF and Jacks T (2012 ) Expression of tumour‐specific antigens underlies cancer immunoediting. Nature 482, 405–409.
Not in our library10.1038/nature10803
- 40.
Eyles J, Puaux AL, Wang X, Toh B, Prakash C, Hong M, Tan TG, Zheng L, Ong LC, Jin Y et al (2010 ) Tumor cells disseminate early, but immunosurveillance limits metastatic outgrowth, in a mouse model of melanoma. J Clin Invest 120, 2030–2039.
Not in our library10.1172/jci42002
Cited by papers we hold 6
- Colorectal liver metastasis: molecular mechanism and interventional therapy · 2022No notice
- A single-cell atlas of liver metastases of colorectal cancer reveals reprogramming of the tumor microenvironment in response to preoperative chemotherapy · 2021Corrected
- Epithelial NOTCH Signaling Rewires the Tumor Microenvironment of Colorectal Cancer to Drive Poor-Prognosis Subtypes and Metastasis · 2019No notice
- EphB2 stem-related and EphA2 progression-related miRNA-based networks in progressive stages of CRC evolution: clinical significance and potential miRNA drivers · 2018Not checked
- CMScaller: an R package for consensus molecular subtyping of colorectal cancer pre-clinical models · 2017No notice
- NLRP3 inflammasome activation promotes inflammation-induced carcinogenesis in head and neck squamous cell carcinoma · 2017No notice
Reads
Read by people on this page
None yet.
Checked or read by AI through naulon
None yet.
A person counts once a day per paper. We keep no cookie and no address: a reader is a hash that changes every day. Any month under five reads shows no number.
Are you an author?
Is this your paper?
Claim it to add your note and be paid when agents cite it. Free.