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
收藏
页数:10
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