| Literature DB >> 26049023 |
Luigi Marano1, Rita Chiari2, Alessio Fabozzi3, Ferdinando De Vita3, Virginia Boccardi4, Giandomenico Roviello5, Roberto Petrioli5, Daniele Marrelli6, Franco Roviello6, Alberto Patriti7.
Abstract
Despite significant improvements in systemic chemotherapy over the last two decades, the prognosis of patients with advanced gastric and gastroesophageal junction adenocarcinoma (GC) remains poor. Because of molecular heterogeneity, it is essential to classify tumors based on the underlying oncogenic pathways and to develop targeted therapies acting on individual tumors. High-quality research and advances in technology have contributed to the elucidation of molecular pathways underlying disease progression and have stimulated many clinical studies testing target therapies in an advanced disease setting. In particular, strong preclinical evidence for the aberrant activation of the HGF/c-Met signaling pathways in GC cancers exists. This review will cover the c-Met pathway, the mechanisms of c-Met activation and the different strategies of its inhibition. Next, we will focus on the current state of the art in the clinical evaluation of c-Met-targeted therapies and the description of ongoing randomized trials with the idea that in this disease, high quality translational research to identify and validate biomarkers is a priority task.Entities:
Keywords: Advanced gastric cancer; Anti-c-Met drugs; Hepatocyte growth factor; Molecularly targeted agents; c-Met positive gastric cancer
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Year: 2015 PMID: 26049023 DOI: 10.1016/j.canlet.2015.05.028
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679