4.6 Article

Molecular pathogenesis, targeted therapies, and future perspectives for gastric cancer

期刊

SEMINARS IN CANCER BIOLOGY
卷 86, 期 -, 页码 566-582

出版社

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.semcancer.2021.12.004

关键词

Cancer organoids; Paligenosis; Precision oncology; Cyclical hit model; Mouse models

类别

资金

  1. American Society of Clinical Oncology (ASCO)
  2. NIH
  3. [DefenseW81XWH-20-PRCRP-CDA]
  4. [2021YIA-8674301298]
  5. [NCIU54 CA163060]

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Gastric cancer is a major cause of global cancer mortality, characterized by molecular diversity and heterogeneous pathogenesis. By studying molecular targeted therapies, immunotherapies, single-cell molecular analyses, and organoid technologies, personalized treatments for gastric cancer can be advanced to improve outcomes and future prevention strategies.
Gastric cancer is a major source of global cancer mortality with limited treatment options and poor patient survival. As our molecular understanding of gastric cancer improves, we are now beginning to recognize that these cancers are a heterogeneous group of diseases with incredibly unique pathogeneses and active oncogenic pathways. It is this molecular diversity and oftentimes lack of common oncogenic driver mutations that bestow the poor treatment responses that oncologists often face when treating gastric cancer. In this review, we will examine the treatments for gastric cancer including up-to-date molecularly targeted therapies and immuno-therapies. We will then review the molecular subtypes of gastric cancer to highlight the diversity seen in this disease. We will then shift our discussion to basic science and gastric cancer mouse models as tools to study gastric cancer molecular heterogeneity. Furthermore, we will elaborate on a molecular process termed palige-nosis and the cyclical hit model as key events during gastric cancer initiation that impart nondividing mature differentiated cells the ability to re-enter the cell cycle and accumulate disparate genomic mutations during years of chronic inflammation and injury. As our basic science understanding of gastric cancer advances, so too must our translational and clinical efforts. We will end with a discussion regarding single-cell molecular analyses and cancer organoid technologies as future translational avenues to advance our understanding of gastric cancer heterogeneity and to design precision-based gastric cancer treatments. Elucidation of interpatient and intratumor heterogeneity is the only way to advance future cancer prevention, diagnoses and treatment.

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