Chalcone Derivatives: Role in Anticancer Therapy

1Cancer is caused by the uncontrolled growth of cells and is a multifactorial disease that claims millions of lives each year worldwide. Its genesis and progression are extremely complex. A variety of strategies are applied to anticancer treatments, including surgery, chemotherapy, and radiotherapy used alone or in combination. However, multidrug resistance (MDR) and side effects constitute major impediments to effective cancer therapy. Phytochemicals, such as chalcones, have been shown to be inexpensive, readily available and relatively nontoxic. Certain chalcones can target key molecular reactions that may induce the genesis and progression of cancer. Thus, scientists are using traditional knowledge of medicinal plants and the sustainable exploitation of marine natural products to synthesize new, more powerful and effective therapeutic antitumor drugs by leveraging different molecular mechanisms.

2A chalcone is a simple chemical scaffold in many natural plant products, including spices, vegetables, fruits, teas. Chalcones, which belong to the flavonoid family and act as intermediates in the biosynthesis of flavonoids, exhibit structural heterogeneity and can act on various drug targets. Chalcone family members have received considerable attention not only because of the possibilities for their synthetic and biosynthetic production but also because of the scope of their biological activities, including anticancer, anti-inflammatory, antidiabetic, cancer chemopreventive, antioxidant, antimicrobial, antileishmanial and antimalarial activities. More importantly, several chalcone compounds have been approved for market and clinical use for various health conditions [e.g., as metochalcone-choleretic/diuretics (1); sofalcone-based anti-ulcer/mucoprotectives (2); and hesperidin methylchalcone-vascular protectives (3)], exemplifying the clinical potential of chalcones (Figure 1).

3Chalcone compounds have a chemical scaffold of 1,3-diaryl-2-propen-1-one, which can be conveniently modified to alter the biological activities of these molecules. By adding various functional groups (aryls, halogens, hydroxyls, carboxyls, phenyl, etc.), which enable chalcone binding with different molecular targets and, as compounds, interaction with other molecules, chalcones exhibit a broad spectrum of biological activities. Therefore, chalcones are useful templates for the development of novel anticancer agents. Moreover, hybridization of the chalcone moiety with other anticancer pharmacophores produces hybrids that have the potential to overcome drug resistance and improve therapeutic specificity, rendering it a promising strategy for developing novel anticancer agents. In this review, we focus on the medicinal chemistry strategies employed for the design and development of anticancer chalcones. The multiple mechanisms of anticancer activities exhibited by chalcones and their therapeutic potential are also summarized herein.

4Chalcone compounds have a chemical scaffold of 1,3-diaryl-2-propen-1-one in trans- (4) or cis- (5) isomers with two aromatic rings (rings A and B) that are joined by a three-carbon unsaturated α,β-carbonyl system (Figure 2). In most cases, the trans isomer is thermodynamically more stable, and therefore, it is the predominant configuration among chalcones. In addition, chalcones contain many replaceable hydrogens, which enables the use of various methods and schemes for the synthesis of chalcone derivatives. In each of these methods, the most important part is the condensation of two aromatic systems (with nucleophilic and electrophilic groups) to yield the chalcone scaffold. The reaction scheme used in the synthesis of the standard scaffold of chalcones (1,3-diphenyl-2-propen-1-one) includes Claisen–Schmidt condensation, carbonylative Heck coupling reaction, coupling reaction, Sonogashira isomerization coupling reaction, continuous-flow deuteraction reaction, Suzuki–Miyaura coupling reaction, one-pot synthesis and solid acid catalyst-mediated reaction. Amongst all methods, the Claisen–Schmidt condensation (Scheme 1) is one of the most common. Thus, the chalcone moiety is a useful template for the development of novel anticancer agents. In addition to the potent anticancer activity of naturally occurring chalcones, three-pronged strategies are employed for the synthesis of anticancer chalcone: structural manipulation of two aryl rings, the substitution of aryl rings to generate heteroaryl scaffolds, and/or molecular hybridization through conjugation with other pharmacologically interesting scaffolds to enhance the molecular anticancer properties (Figure 3).

5Chalcones constitute the core of many natural biological compounds and have been extensively studied for decades. The chalcone family has a wide range of structural diversity and can be roughly classified into two categories: simple/classical chalcones and hybrid chalcones with the core 1,3-diaryl-2-propen-1-one scaffold. They are widely distributed in various parts (roots, rhizomes, heartwood, buds, leaves, flowers, and seeds) of species of genera Angelica, Sophora, Glycyrrhiza, Humulus, Scutellaria, Parartocarpus, Ficus, Dorstenia, Morus, Artocarpus, and so forth. Most natural chalcones occur in monomeric form. Their great structural diversity stems from the number and position of various substituents. Some prominent examples of this class of anticancer chalcones have been isolated from natural sources, such as isoliquiritigenin, butein, and isobavachalcone, and their potential anticancer activities are described herein (Figure 4).

6Isoliquiritigenin (6) (2′,4′,4-trihydroxychalcone, ISL) is one of the most important bioactive compounds with a chalcone structure isolated from licorice roots. ISL is known to have therapeutic potential against various cancers, including breast cancer, colon cancer, gastrointestinal cancer, lung cancer, ovarian cancer, leukemia, and melanoma. Furthermore, ISL not only inhibits cancer cell migration and invasion by suppressing cell proliferation, inducing apoptosis and autophagy, arresting the cell cycle, inhibiting angiogenesis and obstructing metastasis, but can also enhance chemosensitivity.

7Butein (7), a biologically active flavonoid, is derived from the bark of Rhus verniciflua Stokes and exhibits significant anticancer activity in many types of cancers. Butein shows anticarcinogenic action in non-small cell lung cancer (NSCLC) through endoplasmic reticulum stress-dependent Reactive Oxygen Species (ROS) generation and an apoptosis pathway both in vivo and in vitro. In addition, butein induces G2/M phase cell cycle arrest by inhibiting Aurora B and histone H3 phosphorylation in hepatocellular carcinoma (HCC). Butein is also involved in G2/M phase arrest and apoptosis by increasing the phosphorylation of ataxia telangiectasia mutated (ATM) and checkpoint kinase-1 and 2 (Chk1/2), thereby reducing cell division cycle 25C (cdc25C) levels in HCC. Moreover, butein can attenuate angiogenesis, cell invasion/metastasis, and inflammation by inhibiting the nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) signal pathway.

8Isobavachalcone (8) (IBC) is one of the most useful active compounds among numerous chalcones, and it is predominantly found in plants of the Fabaceae and Moraceae families. IBC exhibits antitumor activity against numerous cancer types. IBC has been found to exhibit antiproliferative and proapoptotic activities in HCC by targeting the extracellular signal-regulated kinases (ERKs)/ribosomal S6 kinase 2 (RSK2) signaling pathway. Moreover, IBC has been found to induce ROS-mediated apoptosis by targeting thioredoxin reductase 1 (TrxR1) in human prostate cancer. IBC has also been demonstrated to inhibit cell proliferation and induce apoptosis by suppressing the AKT/glycogen synthase kinase 3β (GSK3β)/β-catenin pathway in colorectal cancer cells. Additionally, IBC can inhibit estrogen receptor alpha (ERα) and decrease CD44 antigen expression, which leads to decreased paclitaxel resistance in ER+ breast cancer. Studies have also reported that IBC inhibits tumor formation in mouse skin cancer and induces apoptosis in neuroblastoma.

9The successful and significant use of naturally occurring chalcones as potential anticancer agents has inspired many efforts directed to developing novel synthetic chalcones with anticancer properties. Furthermore, investigations into the molecular modification of the chalcone structure have promoted chemical alterations, which lead to improved chalcone physicochemical properties and biological profiles. Among the molecular modification strategies used, structural manipulation of both aryl rings, replacement of aryl rings with heteroaryl/alicyclic/steroidal scaffolds and molecular hybridization are the most widely used examples. The standard scaffold in chalcones (1,3-diphenyl-2-propen-1-one) is the most widely researched chalcone structure for its potential anticancer activity. Structural manipulations of 1,3-diphenyl-2-propen-1-one are mostly focused on the phenyl rings (A and B). We summarize the effects of structure–activity relationship (SAR) substitution patterns on chalcone anticancer properties in the next section, including electron-donating (-OH and -OCH3), electron-withdrawing (-Cl, -Br, and -F) and chalcone–metal complexes (Figure 5).

10Similar to naturally occurring chalcones, hydroxyl and methoxy groups added to specific positions on the phenyl ring contribute to the anticancer activity of synthetic compounds. A recent study found that 2′-hydroxy-2,5-dimethoxychalcone (9, half-maximal inhibitory concentration [IC50]: 9.76-40.83 µM) and 2′-hydroxy-4′,6′-dimethoxychalcone (10, IC50: 9.18–46.11 µM) exhibit antiproliferative and proapoptotic activity in a panel of canine lymphoma and leukemia cell lines. Elkhalifa et al. reported that ((E)-3-(4-(Bis(2-chloroethyl)amino)phenyl)-1-(3-methoxyphenyl)prop-2-en-1-one) (11, IC50: 3.94–9.22 µM) significantly inhibit tumor invasion and migration in triple-negative breast cancer (TNBC) by inducing cell cycle arrest and promoting apoptosis. Moreover, Kachadourian et al. demonstrated that (E)-3-(2-chlorophenyl)-1-(2-hydroxy-4,6-dimethoxyphenyl)prop-2-en-1-one (12), an alternate structure of 30 synthetic chalcone derivatives, can induce NF-E2-related factor 2 (Nrf2) transcriptional activity and increase intracellular levels of glutathione (GSH). Kong et al. sought to determine whether methoxylated chalcone analogs of combretastatin A-4, the boronic acid chalcone (13, the concentration that causes 50% growth inhibition [GI50]: 10–200 nm), which involve reversible, high-affinity binding at the colchicine site of tubulin, show prominent anticancer activity in a variety of cancer cell lines. These methoxylated chalcone studies indicated that the number and position of methoxy substituents on the aromatic rings seem to play important roles in cytotoxicity.

11A series of halogen-bearing chalcones (14, the median cytotoxic concentration [CC50]: 1.6–18.4 µM) that combine a basic chalcone framework with a halogen moiety (F, Cl, Br, etc.) have been found to exhibit significant, remarkable cytotoxic potencies and selective toxicity for tumors. Zhang et al. reported a novel brominated chalcone derivative (15, IC50: 3.57–5.61 µM) with antiproliferative activity in gastric cancer cells in vitro and in vivo involving ROS-mediated upregulation of death receptors death receptors 5 (DR5) and DR4 expression and apoptosis. Moreover, Padhye et al. found that fluorinated chalcones (16, IC50: 18.67 µM and 26.43 µM) show more potent antioxidant and antiproliferative activity against human pancreatic BxPC-3 cancer cells and human breast cancer BT-20 cells than their hydroxyl counterparts.

12In recent years, chalcone–metal complexes have attracted widespread attention in bioinorganic medicinal chemistry due to their chelation/coordination properties with various metals and their regulatory effects on various anticancer targets. A recent study found that new Ru(II)-DMSO (17, IC50: 15–28.64 µM) complexes with substituted chalcone ligands show significant anti-breast-cancer activity by inhibiting DNA topoisomerase. Similarly, Jovanovic et al. reported that two thiophene-substituted chalcone–ruthenium complexes with the general formula cis-[Ru(S-DMSO)3(R-CO-CH=CH-R’)Cl] (18, IC50: 22.9–76.8 µM) act as anticancer agents in HeLa cells (human cervical cancer cells) with cytotoxic and proapoptotic activity that can remarkably inhibit topoisomerase II and strongly bind with DNA. Moreover, Samia et al. synthesized palladium (19a), platinum (19b), gold (19c), and copper (19d) complexes with (E)-3-(4-bromophenyl)-1-(pyridin-2-yl)prop-2-en-1-one thiosemicarbazone (HPyCT4BrPh) and explored the cytotoxic potential against HL-60 (human promyelocytic leukemia), THP-1 (human monocytic leukemia) cells, MDAMB-231 (human metastatic breast cancer cell line) and MCF-7 (Michigan Cancer Foundation-7 human breast adenocarcinoma) cell lines (IC50: 0.16–1.27 µM). The coordination of HPyCT4BrPh complexes to copper and gold has been proven to lead to high antitumor activity.

13Hybrid molecules have the potential not only to overcome drug resistance but also to exhibit increased activity and enhanced specificity. Therefore, hybridization of the chalcone moiety with other anticancer pharmacophores is a promising method for developing novel anticancer agents. Recently, a number of chalcone hybrids have been prepared and evaluated for their anticancer activity; some were found to have remarkable activity both in vitro and in vivo, exhibiting their potential as anticancer drugs.

14Artemisinin derivatives bear a peroxide-containing sesquiterpene lactone moiety and can produce highly reactive free radicals (peroxyl free radicals and ROS) in the presence of ferrous ions (Fe[II]). As tumor cells contain a much higher level of Fe[II] ions than healthy tissue cells, artemisinin derivatives can induce the formation of peroxyl free radicals and ROS and oxidative stress, DNA damage and selective apoptosis of cancer cells. Therefore, hybridization of artemisinin and chalcone may provide novel anticancer candidates that not only induce potent toxicity in cancer cells but also exhibit high safety levels in normal cells. The chemical structures of artemisinin–chalcone hybrids are shown in Figure 6.

15Smit et al. synthesized a series of artemisinlcone hybrids (20, IC50: 1.02–53.7 µM) and found not only a potent effect against intraerythrocytic Plasmodium falciparum parasites but also considerable activity against TK-10 (renal), UACC-62 (melanoma), and MCF-7 cancer cell lines. α-Configurated artemisinin–chalcone hybrids (22, IC50: 0.10–29 µM) and β-configurated analogs (21, IC50: 1.7–27 µM; 23, IC50: 0.09–23 µM) also showed greater antiproliferative and cytotoxic effects than dihydroartemisinin against HT-29 (human colon cancer cell), A549, MDA-MB-231, HeLa, and H460 (human lung cancer cell) cancer cell lines. Similarly, a novel series of artemisinlcone hybrids (24, 25) prepared by Gaur et al. showed potent activity against HL-60 (leukemia), Mia PaCa-2 (pancreatic cancer), PC-3 (prostate cancer), LS180 (colon cancer) and HEPG2 (hepatocellular carcinoma) cancer cell lines with a high selectivity index. Kapkoti et al. designed 1,2,3-triazole-containing artemisinin–chalcone hybrids (26, IC50: 7.16–57.18 µM; 27, IC50: 17.14–69.67 µM) displaying remarkable activity against K562 (human chronic myeloid leukemia cell), PC-3 (human prostate cancer cell), A431 (human skin squamous cell carcinoma), MDA-MB-231 (human metastatic breast cancer cell line), COLO-205 (human colon cancer cell), A549 (human lung cancer cell), and HEK-293 (human embryonic kidney cell) cancer cell lines with significant induction of ROS formation. Moreover, a toxicity study on human erythrocytes revealed that these molecules are nontoxic (IC50: >100 μg/mL).

16Azoles constitute a class of five-membered nitrogen-containing heterocyclic compounds with electron-rich properties that includes imidazole, oxadiazole, pyrazole, tetrazole, thiazole, 1,2,3-triazole, and 1,2,4-triazole. Azoles are common pharmacophores used in the development of novel anticancer agents. Recently, a chalcone hybridized with an azole moiety showed significant potential as a novel anticancer agent (Figure 7). A series of chalcone–imidazole hybrids (28, IC50: 1.123–20.134 µM) bearing benzamide or benzenesulfonamide moieties (29, IC50: 0.597–19.995 µM) synthesized by Wang et al. display potential activity against HCT116, MCF-7, and 143B cancer cell lines in vitro. Molecular docking studies and enzymatic assays demonstrated that cathepsin (Cat) L and Cat K might be potential targets for these hybrids. Chalcone–oxadiazole hybrids (30, GI50: 0.32–11.0 µM) have also shown broad spectrum activity against a series of 60 cancer cell lines, particularly leukemia cells. Furthermore, these synthesized compounds can inhibit epidermal growth factor receptor (EGFR) (IC50: 0.24 µM), proto-oncogene tyrosine-protein kinase (Src) (IC50: 0.96 µM), and interleukin-6 (IL-6) (% of control: 20%) and might play anticancer roles in various cancers.

17Moreover, Hawash et al. reported that chalcone-pyrazole hybrids (31, IC50: 0.5–4.8 µM) cause cell cycle arrest in G2/M phase followed by apoptotic cell death and impaired cell growth in HCC cell lines, indicating that these hybrids may be considered potential chemotherapeutic agents for the treatment of HCC. A majority of chalcone–tetrazole hybrids (32, IC50: 0.6–3.7 μg/mL; 33, IC50: 2.5–31.4 μg/mL; 34, IC50: 12.0–42.4 μg/mL) have been shown to exert superior activity against colon HCT116, prostate PC-3, and breast MCF-7 cancer cell lines than cisplatin or fluorouracil.

18Treatment with drug-resistant cell lines (CEM/ADR5000, MDA-MB-231/BCRP, HCT116(p53−/−), and U87MG/ΔEGFR cells) with thiazole-containing chalcone derivatives (35, IC50: 2.72–41.04 µM) was found to induce significant hypersensitivity effects, suggesting that these compounds are suitable molecules to combat the drug resistance of cancer cells. Triazole has two structures: 1,2,3-triazole and 1,2,4-triazole. Both of these forms have shown potential as novel anticancer candidates. Both of them have shown their potential as novel anticancer candidates. Hussaini et al. synthesized a series of chalcone-1,2,3-triazole hybrids (36, GI50: 1.3–186.2 µM) with the same substituents as combretastatin-A4, which can lead to the accumulation of A549, HeLa, DU145, and HepG2 cancer cell lines in the G2/M phase, inhibit tubulin polymerization, and trigger apoptosis by inducing changes to the mitochondrial membrane potential and activating caspases 3 and 9. Moreover, Ahmed et al. prepared a series of novel 1,2,4-triazole/chalcone hybrids (37, IC50: 4.4–16.04 µM) that can induce the apoptosis of human lung adenocarcinoma A549 cells through a caspase-3-dependent pathway.

19Coumarin derivatives have been shown to exhibit a variety of anticancer mechanisms, and some of these derivatives, such as irosustat, are in clinical trials for multiple cancer treatments, exhibiting their potential as putative anticancer drugs. Thus, hybridization of chalcone with coumarin may produce attractive novel anticancer candidate agents (Figure 8). A recent report by Wang et al. demonstrated that a series of coumarlcone hybrids can decrease TrxR expression and significantly induce ROS accumulation to activate the mitochondrial apoptosis pathway. The representative hybrids (38, IC50: 3.6 μM) have exhibited higher antitumor activity against HCT116 cells than xanthohumol (Xn). Sinha et al. also reported chalcone–coumarin hybrids (39, S009-131) that show potential antiproliferation activity against cervical cancer cells (HeLa (IC50: 4.7 μM) and C33A (IC50: 7.6 μM)) by inducing apoptosis and arresting the cell cycle at G2/M phase. This molecule induces an increase in the Bax/Bcl-2 ratio and intracellular ROS and then releases cytochrome c into the cytosol to activate the initiator caspase-9 and executioner caspase-3/7. Moreover, the tumor suppressor protein p53 and its transcriptional target p53 upregulated modulator of apoptosis (PUMA) are upregulated, suggesting their role in mediating cell death. In addition, chalcone–coumarin hybrids (40, IC50: 0.65–2.02 μM) have been shown to exert significant cytotoxic activity against HEPG2 liver cancer and K562 leukemia cells. Interestingly, these hybrids can also induce apoptosis by activating caspases 3 and 9. In addition, chalcone–coumarin hybrids (41, GI50: 22.11–41.08 μM) have been found to have antiproliferative activity in breast cancer cell lines (MDA-MB231, MDA-MB468, and MCF7 cells), which is comparable to cisplatin (GI50: 23.65–31.02 μM).

20Due to the versatile nature of indoles, a variety of indole derivatives have been recently designed as anticancer agents that act via different mechanisms of action as histone deacetylases (HDACs), sirtuins, and DNA topoisomerase, etc.. Several indole-containing drugs, such as semaxanib and sunitinib, have been used in the clinic for cancer treatment, and chalcone–ndole hybrids may represent a promising strategy to produce novel anticancer candidates (Figure 9). Chalcone–indole hybrids (42, IC50: 0.23–1.8 μM) synthesized by Wang et al. have been shown to display potent cytotoxic activity against all tested cancer cell lines, including drug-sensitive HepG2, SMMC-7221, PC-3, A549, K562, HCT116, SKOV3, and MCF-7, drug-resistant HCT-8/T (resistant to paclitaxel) and HCT-8/V (resistant to vincristine) cancer cells. The growth of tumors in hybrid-treated mice has been shown to be inhibited in an in vivo HepG2 hepatocarcinoma mouse model. Moreover, these molecules markedly induce cell cycle arrest in the G2/M phase and inhibit the polymerization of tubulin. Yan et al. also reported indole-chalcone derivatives (43, IC50: 45–782 nM; 44, IC50: 23–77 nM; 45, IC50: 3–679 nM) that exhibit potent antiproliferation activity in A549, HeLa, Bel-7402, MCF-7, A2780, and HCT-8 cancer cells. A further mechanistic study demonstrated that this hybrid induces low levels of cytotoxicity in normal human cells and exhibit metabolic stability in mouse liver microsomes. It also can inhibit tumor growth in xenograft models in vivo without apparent toxicity. Cellular mechanism studies elucidated that this hybrid is a novel tubulin polymerization inhibitor that binds to the colchicine site, arresting the cell cycle in the G2/M phase and inducing apoptosis along with a decrease in the mitochondrial membrane potential. Cong et al. explored the anticancer potential of indole-chalcone derivatives (46, FC77, GI50: 1–53.4 nM) against a panel of MDR cancer cell lines, including HL60/DOX (doxorubicin-resistant), K562/HHT300 (homoharringtonine-resistant), CCRF-CEM/VLB100 (vinblastine-resistant), A549/T (paclitaxel-resistant), A549/DDP (cisplatin-resistant) and HCT-116/L (oxaliplatin-resistant) cells. Several of these MDR cancer cell lines show no resistance to these indole-chalcone derivatives. Further investigation revealed that this molecule can arrest cells that are involved in tubulin-binding and inhibit microtubule dynamics. Taken together, these studies show that chalcone-indole hybrids can potentially serve as novel microtubule-targeting agents for the further development of potential drug candidates for the treatment of MDR cancers.

21In addition to the aforementioned chalcone hybrids, other hybrids, such as chalcone–ferrocene, chalcone–furan/thiophene hybrids, chalcone–pyridine/pyrimidine hybrids, chalcone–quinoline/quinolone hybrids, chalcone–quinoxaline/quinazolinone hybrids, chalcone-quinone hybrids, chalcone–triazine hybrids, and chalcone–dithiocarbamate hybrids also showed certain anticancer activity.

22Many efforts have been made to characterize the mechanism of action of chalcone compounds. Their multitarget and broad-spectrum biological activities have been reviewed in previous papers. On the other hand, the extensive biological activity spectrum of chalcones also indicates their potential for confounding targeted treatment, posing a challenge to chalcone clinical development. Thus, understanding the mechanisms of chalcones and their direct molecular targets is particularly important for the development of clinically useful chalcone compounds in the future. This section, therefore, presents a summarizes of the representative mechanisms of the anticancer action of chalcones reported in recent years (Figure 10).

23The tumor protein p53 modulates the cell cycle and functions as a tumor suppressor. p53 plays important roles in maintaining cellular and genomic integrity and preventing the proliferation of incipient cancer cells. p53 is degraded by various compounds, such as the mouse double minute 2 (MDM2) and Sirtuin-1. Inhibition of p53 protein degradation is a critical strategy in anticancer therapy (Table 1).

24MDM2 is the most notable negative regulator of p53. MDM2, an E3 ubiquitin ligase, downregulates p53 activity by constantly monoubiquitinating p53, which is an important step in mediating its degradation by nuclear and cytoplasmic proteasomes. Thus, disruption of p53-MDM2 is the key event in p53 activation. Silva et al. found that trans-chalcone (TChal) (1) could downregulate Specificity proteins 1 (Sp1), a transcription factor involved in cell proliferation and differentiation, and upregulate p53 expression in U2OS osteosarcoma cells. However, Dos et al. reported that series of chalcones with halogens on ring B and additional benzene rings (47 IC50: 13.2–34.7 μM, Figure 11) showed antiproliferative activity against breast cancer cells (MCF-7 and MDA-MB-231), with upregulation of p53 and showed no effect on Sp1 protein expression. Further mechanistic studies demonstrated that TChal could bind and degrade chromosome region maintenance 1 (CRM1), a nuclear export receptor involved in the active transport of tumor suppressors, and increase heat-shock protein 40 (HSP40) expression in U2OS osteosarcoma cells; the interaction of HSP40 with MDM2 blocked MDM2-mediated ubiquitination of p53, leading to the enhanced stability and activation of p53. Moreover, Siqueira et al. reported that TChal could reestablish the p53 pathway and prevent the overexpression of Wnt/β-catenin tumor development, inducing autophagy-related cell death and decreasing the metastatic capacity of HCC HuH7.5 cells. Seba et al. reported that the chalcone derivative 4′-aminochalcone (48) inhibited the migration and invasion of osteosarcoma cells through the inhibition of extracellular matrix enzymatic degradation and the modulation of p53, regulating the epithelial-mesenchymal transition (EMT)-related genes.

25A coumarlcone hybrid (39, S009-131) synthesized by Sashidhara et al. could induce the DNA damage response and trigger p53 activation through the phosphorylation of its key residues. Further mechanistic studies showed that the p53-MDM2 interaction was disrupted by DNA damage-induced phosphorylation. In addition, docking studies demonstrated that this hybrid could occupy the p53-binding pocket of MDM2 and increase cellular p53 levels. Interestingly, Cabral et al. reported that a novel chalcone-like compound (49, LQFM064) exhibited cytotoxic activity against MCF7 cells (IC50: 21 μM) by inducing cell cycle arrest at the G0/G1 phase with increased p53 and p21 expression. However, the compound did not interfere directly with p53/MDM2 complexation in MCF7 cells but activated both apoptotic pathways via the modulation of proteins involved in the extrinsic and intrinsic pathways, exhibiting an increase in tumor necrosis factor receptor-1 (TNF-R1), Fas ligand (Fas-L) and Bax levels and a reduction in Bcl-2 expression. Taken together, these studies suggested that the diverse chemical structures of chalcones may contribute to their differential effects mediated through the p53 pathway.

26Tubulin is a dimeric protein consisting of two similar, nonidentical subunits: α and β. The discovery of chalcones as antimitotic agents was first reported nearly 30 years ago. Based on the understanding of the colchicine-tubulin structure–activity relationship, chalcone derivatives are modeled as colchicine analogs, which can bind to tubulin and prevent its polymerization, leading to abrupt interruption of mitotic spindle assembly, interference with the function of the cytoskeleton, and interrupted mitosis. The structure–activity relationships of numerous chalcone derivatives have since been studied with colchicine and vinblastine as controls (Table 2).

27Numerous chalcones have demonstrated a capacity for binding β-tubulin similar to that of combretastatin 4A, destabilizing microtubule polymers and thus serving as combretastatin 4A analogs. Ducki et al. synthesized and developed CA-4 type chalcones SD400 (50) and α-phenyl chalcone (51) (Figure 12), which displayed potent inhibition of tubulin polymerization with arrest in the G2/M phase and showed promising antivascular activity. Kamal et al. reported that a series of phenstatin/isocombretastatin–chalcones (52, GI50: 0.11–19.0 μM) displayed potent antiproliferative activity in a panel of sixty human cancer cell lines. A competitive binding assay suggested that these compounds were bound to the colchicine-binding site of tubulin, inducing potent inhibitory effects on tubulin assembly and leading to arrest in the G2/M phase and apoptotic cell death. Moreover, Kode et al. found that new phenstatin-based indole-linked chalcone compounds (53, GI50 < 0.1 µM) showed anticancer activity in SCC-29B human oral cancer cells, spheroids and AW13516 oral cancer xenograft model mice. Further mechanistic studies revealed that these compounds destabilized tubulin, leading to loss of cell integrity and affecting glucose metabolism. In addition, surface plasmon resonance confirmed direct molecular interactions between tubulin and these compounds. A novel chalcone-1,2,3-triazole derivative (54) synthesized by Yan et al. showed significant antitumor activity against liver cancer HepG2 cells in vitro with an IC50 value of 0.9 μM and in vivo with low toxicity in mice. Moreover, they found that this derivative might be a potent tubulin polymerization inhibitor. Canela et al. reported a new chalcone, called TUB091 (55), that binds to the colchicine site of tubulin, as shown by X-ray crystallography. TUB091 inhibited cancer and endothelial cell growth and induced G2/M phase arrest and apoptosis at 1-10 nM. Furthermore, TUB091 showed vasculature disruption both in vitro and in melanoma and breast cancer xenograft models. Alswah et al. reported that triazoloquinoxaline-chalcone derivatives (56, IC50: 1.65–34.28 µM) displayed significant antiproliferative effects against MCF-7, HCT-116 and HEPG-2 cells. A molecular docking study demonstrated that the binding modes of these chalcones were targeted to epidermal growth factor receptor tyrosine kinase (EGFR-TK) and tubulin. Moreover, Mphahlele and his coworkers found that 2-arylbenzo[c]furan-chalcone hybrids (58) showed the potential to exhibit inhibitory effects against tubulin polymerization and EGFR-TK phosphorylation. In summary, chalcones can be considered attractive tubulin polymerization inhibitor candidates for developing anticancer therapeutics.

28The nuclear factor kappa B (NF-κB) is a crucial transcription factor that plays an important role in inflammation, innate immunity and carcinogenesis. NF-κB signaling was shown to contribute to cancer progression through the upregulation of tumor-promoting cytokines and survival genes (e.g., Bcl-2), inhibition of apoptosis, and promotion of angiogenic factors, and it manifests a migratory and invasive phenotype. Thus, NF-κB inhibitors mediated effects that could lead to an antitumor response or to moresensitive antitumor drug action. NF-κB activity is regulated primarily by IκB kinases (IKKs), which are recognized as the central mediators of immune responses and inflammation. Interference of NF-κB function through IKK inhibition is expected to suppress NF-κB protein translocation to the nucleus and is considered a promising strategy for disease treatment, especially against inflammation and inflammation-related cancer.

29Chalcones demonstrate NF-κB inhibitory activity by inducing the covalent modification of IKK proteins via an α,β-unsaturated ketone with Michael-type activity (Table 3). Indeed, Pandey et al. reported that butein (3,4,2’,4’-tetrahydroxy chalcone) (7) suppressed NF-κB activity and NF-κB-regulated gene expression by conjugating the cysteine 179 residue of IKK and then blocking the phosphorylation and degradation of IκBα. Similarly, 2-hydroxy-3’,5,5’-trimethoxychalcone (DK-139) (58, Figure 13) inhibited the Toll-like receptor 4-mediated inflammatory response through suppression of the Akt//IKK/NF-κB signaling pathway in BV2 microglial cells. In addition, isoliquiritigenin, flavokawain A and B, licochalcone A, cardamonin and xanthohumol all showed anti-inflammatory and anticancer activities by preventing the degradation of IκBα and in turn blocking NF-κB activation. Moreover, Venkateswararao et al. evaluated the inhibitory activity of a series of chalcone derivatives (59, IC50: 1.17–3.43 µM) against NF-κB and their in vitro antiproliferative activity against various human cancer cell lines, and they found a good correlation between NF-κB inhibition through these derivatives and antiproliferative activity. Gan et al. also designed two novel dihydrotriazine-chalcone compounds (60) previously found to exert antiproliferative effects through dual targeting of dihydrofolate reductase (DHFR) and TrxR, which could inhibit the in vitro migration of MDA-MB-231 breast carcinoma cells through dose-dependent downregulation of matrix metalloproteinase-9 (MMP-9) expression and secretion. Moreover, these chalcone-based compounds inhibited inflammatory mediator expression, including inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) and tumor necrosis factor alpha (TNF-α), through suppression of the NF-κB signaling pathway. In conclusion, chalcones can be developed as novel scaffolds that target both invasion and inflammation to develop chemopreventive and/or anticancer therapies.

30Angiogenesis is a promising target for cancer treatment due to its important role in cancer progression and metastasis. Chalcones were recently documented to modulate several steps in angiogenesis, such as vascular endothelial factor (VEGF), basic fibroblast growth factor (bFGF), transforming growth factor-β (TGF-β) signaling pathway or hypoxia-inducible factor-1 (HIF-1), MMP activity or endothelial cell proliferation and migration (Table 4).

31Ma et al. found that a 3′,5′-diprenylated chalcone (61, Figure 14) likely showed friend leukemia integration-1 (Fli-1) agonism and regulation of the expression of VEGF-1, TGF-β2, intercellular cell adhesion molecule-1 (ICAM-1), p53, and MMP-1 genes, which are associated with tumor apoptosis, migration, and invasion in prostate cancer cells. Iheagwam et al. performed a molecular docking analysis, also showing that flavonoids (62) isolated from young Caesalpinia bonduc twigs and leaves displayed strong interactions with TK, VEGF, and MMP. Wang et al. screened nearly 36,043 compounds and found that isoliquiritigenin (6) exhibited the most potent antiangiogenic activities in zebrafish with the concentration for 50% of maximal effect (EC50) values of 5.9 μM. Mechanistically, isoliquiritigenin inhibited arachidonic acid (AA) metabolic enzymes, including COX-2, microsomal prostaglandin E synthase-1 (mPGES-1) and cytochrome P450 (CYP) 4A11, in glioma and resulted in the inhibition of the angiogenic Akt-FGF-2/TGF-β/VEGF signaling pathway through ceRNA effects on miR-194-5p and lncRNA NEAT1. Moreover, Wang et al. also found that isoliquiritigenin could inhibit breast cancer growth and neoangiogenesis accompanied by VEGF/VEGFR-2 signaling suppression, an elevated apoptosis rate and few toxicity effects both in vitro and in vivo. Molecular docking simulation indicated that isoliquiritigenin could stably form hydrogen bonds and aromatic interactions within the ATP-binding region of VEGFR-2. Kwon et al. demonstrated that the oral administration of licochalcone E (LicE) (63) significantly inhibited solid tumor growth and lung metastasis of mammary cancer cells, which was associated with suppression of tumor angiogenesis and lymphangiogenesis, as well as a decrease in inflammatory status in the tumor and lung (the target organ) tissues. In addition, Saito et al. found that xanthohumol (64), a prenylated chalcone in hops (Humulus lupulus L.), blocked angiogenesis in pancreatic cancer by reducing both NF-κB activity and the subsequent production of angiogenic factors VEGF and IL-8 in vitro and in vivo.

32In addition to the inhibitory effect of chalcones on VEGF, chalcones also demonstrated potential inhibitory activity against other angiogenic factors. Wang et al. synthesized a novel series of chalcone derivatives (65), and a tested compound exhibited significant inhibitory effects on HIF-1. In addition, the tested compound inhibited tumor invasion and angiogenesis in vitro and in vivo with good tolerance and presented a good therapeutic window. Wang and colleagues reported that FLA-16 (66), a novel chalcone-type flavonoid isolated from Glycyrrhiza glabra roots, inhibited CYP4A, prolonged the survival and normalized the vasculature of glioma by decreasing the production of tumor-associated macrophages (TAMs) and endothelial progenitor cell (EPC)-derived VEGF and TGF-β in vitro and in vivo. Jeong et al. also reported that an improved analog of chalcone (67) could suppress the TGF-β1-induced EMT of human A549 lung cancer cells. Stanojkovic et al. found a series of highly selective anthraquinone–chalcone hybrids (68, IC50: 3.87–5.99 μM) showing anti-invasive, antimetastatic, and antiangiogenic properties by decreasing the expression levels of MMP2, MMP9, and VEGF against K562 cells. Moreover, a number of chalcone analogs of combretastatin 4A demonstrated significant effects in tumor blood vessels (for details, see Section 3.2). In summary, the use of chalcones is a potential therapeutic strategy to reduce inflammation and tumor angiogenesis.

33Numerous studies have focused on the ability of chalcone to mediate resistance to conventional chemotherapeutic drugs by modulating multidrug efflux transporters, which are essential components of intracellular drug accumulation. Most of the investigated chalcones showed the ability to inhibit three well-characterized members of the ATP-binding cassette (ABC) transporter family: P-glycoprotein (P-gp, ABCB1), multidrug resistance-associated protein 1 (MRP1, also known as ABCC1), and breast cancer-resistance protein (BCRP, ABCG2), main contributors to the MDR in cancer cells. Therefore, chalcones have received considerable attention as chemosensitizers for clinical drug resistance and for improving the pharmacokinetics of poorly absorbed chemotherapeutic cancer drugs (Table 5).

34In the late 1990s, Bois et al. explored the structural requirements of chalcones for P-gp regulation and found that 2′,4′,6′-trihydroxy-4-iodochalcone and 4-alkoxy-2′,4′,6′-trihydroxychalcones exhibited high-affinity binding for P-gp. Recently, using computer-aided drug design (CADD) methods, including 2D- and 3D-quantitative structure–activity relationships (QSAR), molecular modeling, and docking analyses, Parveen et al. and Ngo et al., reported a series of novel synthesized chalcones (69, IC50: 42 nM; Figure 15) showing high levels of biological activity and indicating the importance of specific groups for P-gp inhibitory effects. Other authors explored the ability of chalcone derivatives to regulate the effects of P-gp on MDR. For example, Gu and colleagues synthesized a series of bifendate–chalcone hybrids (70) and found that the best compound with minimal intrinsic cytotoxicity (IC50 > 200 μM) could increase the accumulation of rhodamine-123 in K562/A02 human leukemia cells more potently than bifendate or verapamil (VRP) by inhibiting P-gp efflux function. Moreover, Yin et al. also reported that a novel chalcone derivative, MY3 (71, IC50: 1.02 μM), not only induced little intrinsic cytotoxicity but also reversed DOX resistance in MCF-7/DOX cells via suppression of P-gp. More importantly, MY3 markedly enhanced the efficacy of DOX treatment in MCF-7 tumor xenografts, without changed model body weight. Li et al. reported that flavokawain A (FKA) (72, IC50: 21 µM) inhibited P-gp protein expression by blocking the PI3K/Akt pathway in paclitaxel (PTX)-resistant A549 (A549/T) cells, indicating that FKA combined with PTX reversed PTX resistance. Furthermore, they used national medical product administration (NMPA)-approved aescinate (Aes) to prepare twin-like nanoparticles (NPs) such as PTX-A NPs and FKA-A NPs, which reversed PTX resistance both in vitro and in vivo by inhibiting P-gp expression in A549/T cells.

35Moreover, the potential modulatory effect of bioactive compounds of chalcones on ABCG2-mediated multidrug resistance has been investigated for years. Wu et al. reported that licochalcone A (LCA) (73), a natural chalcone isolated from the root of Glycyrrhiza inflata, inhibited the drug transport function of ABCG2 and reversed ABCG2-mediated multidrug resistance in human multidrug-resistant cancer cell lines in a concentration-dependent manner. An in silico docking analysis used to discern the role of LCA in the inward-open conformation of human ABCG2 revealed LCA binding ABCG2 in the transmembrane substrate-binding pocket. Kraege et al. synthesized a series of novel heterodimeric modulators based on the combination of chalcones with quinazolines (74), and the most potent ABCG2 inhibitor in this series (IC50: 0.19 μM) was selective, nontoxic (GI50: 93 μM) and able to reverse MDR. Winter and colleagues synthesized symmetric bis-chalcones with different substituted groups and screened them to determine their ability to inhibit mitoxantrone efflux from ABCG2-transfected HEK293 cells. The best derivative (75) was selective for ABCG2 over P-glycoprotein and MRP1 and stimulated ABCG2 basal ATPase activity. Peña-Solórzano et al. found that tariquidar-related chalcones (76) exhibited selectivity for ABCG2 to a greater extent than the transporters ABCB1 and ABCC1. Notably, novel quinolone chalcones (77) synthesized by Lindamulage et al. could overcome multidrug resistance by impeding MRP1 function while maintaining strong inhibition of microtubule activity. This compound exhibited strong anticancer activity, alone or in combination with paclitaxel, without causing any notable side effects in mice engrafted with MDA-MB-231 triple-negative breast cancer cells.

36Interestingly, some studies demonstrated the effect of a dual ABCG2/ABCB1 inhibitor. For example, Boumendjel et al. reported a novel chalcone derivative, JAI-51 (78), acting not only as a microtubule-depolymerizing agent but also as an inhibitor of P-gp and BCRP in vitro and in vivo in glioblastoma models. Han et al. and Cai et al. found that nonbasic chalcone (79) served as a dual ABCG2/ABCB1 inhibitor by inhibiting ABCG2 and ABCB1 ATPase activities, not by altering the expression or localization of the ABCG2 or ABCB1 transporters. Silbermann et al. described two novel chalcone and flavone derivatives (80). One of these inhibitors (80a, IC50: 3.37 μM) was a highly potent reverser of ABCG2-mediated MDR and a parallel dual ABCC1/ABCG2 inhibitor. Another was a highly potent dual ABCB1/ABCG2 MDR reverser. In summary, chalcones might be promising lead compounds to develop as chemosensitizers for clinical drug resistance, as well as for improving the pharmacokinetics of poorly absorbed chemotherapeutic cancer drugs.

37Chalcones have been shown to exhibit anticancer activity through their inhibitory potential against various targets, such as 5α-reductase, aromatase, histone deacetylase inhibitors (HDAC), proteasome, JAK/STAT signaling pathways, cell division cycle 25 (CD25), cathepsin-K, topoisomerase-II, Wnt, ROS/MAPK, p38 and mTOR. However, these studies are not covered in this review because not enough evidence has been provided to indicate that these proteins or pathways are direct targets of chalcones. Therefore, the identification and confirmation of the molecular target(s) of chalcones are important steps in pharmaceutical research. Researchers have invested tremendous effort to explore direct-binding targets of chalcones using a variety of strategies. We discuss the most commonly used experimental methods for target recognition, such as computer strategies.

38Computer strategies, such as QSARs assessments, molecular docking, and virtual screening, have been widely used in research aimed to find the targets of natural and synthetic chalcones. Marquina et al. designed and synthesized eleven 4′-alkoxy chalcones that could induce the mitochondrial apoptotic pathway by regulating Bax and Bcl-2 transcripts and by increasing caspase 3/7 activation. This QSAR model study revealed that the double bond of the α,β-unsaturated carbonyl and the planar structure geometry was important to the biological activity of synthetized chalcones. Song et al. discovered human carboxylesterase 2 (hCES2A) inhibitors obtained from Glycyrrhiza inflata through a combination of docking-based virtual screening and fluorescence-based inhibition assays. hCES2A is a key target to ameliorate the intestinal toxicity triggered by irinotecan, which causes severe diarrhea in 50–80% of patients receiving this anticancer agent. Following the screening of 73 herbal products, Song et al. found that licochalcone C, chalcones and isolicoflavonol in licorice were the key compounds critical for hCES2A inhibition, which will be very helpful in developing new herbal remedies or drugs for ameliorating hCES2A-associated drug toxicity. Molecular docking with corresponding chalcones has also been applied to predict the binding mode and explain the phenotypic activity of EGFR, aurora kinase, anaplastic xanthine oxidase (XO), the colchicine binding site of the tubulin, the estrogen receptor and acetylcholinesterase (AChE). The advantage of using a computational strategy is the convenience of predicting the binding target(s) of chalcones before biological validation. However, the binding site and binding specificity need to be validated.

39Chalcones play central roles in the flavonoid synthesis pathway and are ubiquitous in many natural products. Chalcones exhibit a broad spectrum of biological activity, probably due to their small structure and Michael-acceptor features, making them tolerant of different biological molecules, allowing their ready or reactive binding with certain molecules. In addition, chalcone compounds have a chemical scaffold that can be conveniently modified to alter their overall biological activity. In different screening assays, chalcones have been able to target multiple cellular molecules, such as MDM2/p53, tubulin, NF-κB, ABCG2/P-gp/BCRP, VEGF, VEGFR-2 kinase, and MMP-2/9.

40Despite medicinal applications of chalcones, their wide bioactivity spectrum indicates a potentially promiscuous targeting profile, which presents a challenge for clinical development. Recently, Xing and colleagues found a hepatotoxic risk for flavokawain A (58) and B (59) (Figure 4), two chalcone derivatives isolated from kava used for their anxiolytic and sedative effects and that show hepatotoxic synergism with acetaminophen. Using in silico tools, Tugcu et al. also illustrated the hepatotoxicity potential of kava. According to the experimental results and predictions, kava constituents play substantial roles in hepatotoxicity by mechanisms involving glutathione depletion, CYP inhibition, reactive metabolite formation, mitochondrial toxicity and/or cyclooxygenase activity. Moreover, Qian et al. reported that a licorice monomer compound (2′-HC) at a concentration of ≥20 µM resulted in excess ROS production and inadequate Cu/Zn Superoxide Dismutase (SOD1) expression in hepatocytes. Therefore, the design and synthesis of new analogs are particularly important for the future development of clinically useful chalcone derivatives. Computer strategies and CADD approaches represent time-, labor-, and cost-effective strategies for identifying lead compounds in the early stages of drug discovery.

41Notably, metochalcone has been approved as a choleretic drug, and sofalcone is an anti-ulcer agent that increases the amount of mucosal prostaglandin, conferring a gastroprotective effect against Helicobacter pylori. These drugs represent a promising strategy for developing chalcones as novel anticancer agents. Recently, Jeong et al. and Oh et al. have shown that synthetic chalcones can have a heat-shock protein 90 (HSP90)-induced inhibitory effect, which opens new perspectives into cancer treatment through the destabilization proteins by which cancer cells survive and multiply (tumorigenesis). Several phase II clinical trials of new anticancer molecules that have two hydroxyl groups at positions 1 and 3 have revealed the inhibition of interactions between HSP90 and patient proteins through the binding of these molecules to the ATP site in HSP90. Perhaps in the future, phase III clinical trials will be conducted to support the anticancer potential of chalcones and their derivatives. Interestingly, Song et al. have shown that the combining licochalcone C with irinotecan can ameliorate the intestinal toxicity induced by irinotecan by suppressing hCES2A. Therefore, the combination of chalcones and other therapies is expected to be an effective way to improve anticancer therapeutic efficacy.

42Moreover, for more than half a century, global marine sources have proven to be a rich source of a vast array of new medicinally valuable compounds. However, there is a lack of research on chalcones in marine natural products. De Luca et al. analyzed the microalgal transcriptomes available in the Marine Microbial Eukaryotic Transcriptome Sequencing Project (MMETSP) database for an in silico search of chalcone synthase and 4-Coumarate: CoA ligase, an upstream enzyme in the synthesis of chalcones. They first report the occurrence of these enzymes in specific microalgal taxa. This study gives new insights into possible biotechnological applications for the production of bioactive compounds, such as chalcones.

43In general, chalcones are easy to chemically modify and synthesize to generate compounds with a wide variety of structural diversities. This property makes chalcones very attractive as basic building blocks for the synthesis of molecule-targeting agents. In the coming era of molecularly targeted therapy and personalized medicine, both naturally occurring and synthetic chalcones may be very useful tools for studying basic mechanisms of cancer treatment and prevention and for developing novel agents for targeted cancer therapies.