Current advances of targeting HGF/c-Met pathway in gastric cancer

被引:30
|
作者
Anestis, Aristomenis [1 ]
Zoi, Ilianna [1 ]
Karamouzis, Michalis V. [1 ,2 ]
机构
[1] Univ Athens, Med Sch, Mol Oncol Unit, Dept Biol Chem,Laiko Gen Hosp, Athens, Greece
[2] Univ Athens, Med Sch, Laiko Gen Hosp, Dept Internal Med 1, Athens, Greece
关键词
Gastric cancer; hepatocyte growth factor (HGF); c-Met; molecular targeted therapy; personalized medicine; HEPATOCYTE GROWTH-FACTOR; METASTATIC COLORECTAL-CANCER; TYROSINE KINASE INHIBITORS; LABEL PHASE-3 TRIAL; C-MET; FACTOR-RECEPTOR; DOWN-REGULATION; SIGNALING PATHWAY; MEDIATES RESISTANCE; MONOCLONAL-ANTIBODY;
D O I
10.21037/atm.2018.04.42
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Despite the advances in systemic chemotherapy, gastric adenocarcinoma (GC) remains the third most common cause of cancer-related deaths with poor prognosis. The heterogeneity of GC indicates that novel biomarkers should be established in order to further classify tumors and develop individual targeted therapies. High-quality preclinical and clinical research has demonstrated that growth factor (HGF)-hepatocyte growth factor receptor (c-Met) pathway plays a pivotal role on the growth, survival and invasiveness of GC. In particular, aberrant activation of HGF/c-Met signaling pathway has been associated with poor clinical outcomes, suggesting the therapeutic potential of c-Met. This has stimulated the development and evaluation of a number of c-Met targeted agents in an advance disease setting. In this review, we summarize the current state of the art in the advances on the inhibition of c-Met pathway, with particular emphasis on the clinical testing of c-Met targeted therapeutic agents. Furthermore, we discuss the challenges facing the incorporation of c-Met targeted agents in randomized trials, with the idea that the definition of the appropriate genetic and molecular context for the use of these agents remains the priority.
引用
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页数:10
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