Skip to content
naulon
Not checkedNot checked for notices yet.

Progress in targeted therapy for breast cancer

Jie Ju, An-Jie Zhu, Peng Yuan

Chronic Diseases and Translational Medicine · 2018

doi:10.1016/j.cdtm.2018.04.002 (opens in a new tab)

We email you when a new notice or a question about this paper appears.

Abstract

Breast cancer is a multistep, multifactorial, and heterogeneous disease. Significant transformations have occurred in the systemic management of breast cancer in the past decade. Due to the further understanding of pathogenesis, scientists have found plenty of signaling pathways and correspondingly therapeutic targets in breast cancer, such as hormone receptor, human epidermal growth factor receptor 2 (HER2), epidermal growth factor receptor (EGFR), vascular endothelial growth factor (VEGF), phosphoinositide‐3‐kinase (PI3K), v‐akt murine thymoma viral oncogene homolog (AKT), mechanistic target of rapamycin (mTOR), cyclin‐dependent kinase 4/6 (CDK4/6), poly (adenosine diphosphate‐ribose) polymerase (PARP), and programmed death‐1 (PD‐1). Targeted therapy, which optimizes the accuracy of antitumor activity and minimizes toxicity to normal tissues, plays a crucial role in breast cancer treatment in the era of precision medicine. In this review, we aimed to summarize the latest developments in targeted therapy for breast cancer and discuss the existing problems.

Abstract licence: CC BY-NC-ND

References54

    40 more references, whose wording the paper’s licence keeps private.

    All 54 references

    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.