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- W2016579969 abstract "The receptor tyrosine kinase, c-MET and its ligand hepatocyte growth factor/scatter factor (HGF/SF) have become leading candidates for targeted cancer therapies. Inappropriate c-MET signaling through autocrine, paracrine, amplification, and mutational activation occurs in virtually all types of solid tumors (http://www.vai.org/met), contributing to one or a combination of proliferative, invasive, survival, or angiogenic cancer phenotypes. c-MET and HGF/SF participate in all stages of malignant progression and represent promising drug targets in a variety of cancer types, including carcinomas, sarcomas, and brain tumors. While many are in pre-clinical testing, a few inhibitors have entered clinical trials. With hundreds of thousands of potential responding cancers that express c-MET, the interest in this molecule as a drug target is not surprising. However, the cognate c-MET diagnostic tests lag behind. In addition, despite the great enthusiasm based on response rates in phase I trials, there is a need for caution. It is almost without question that combination therapies with c-MET-HGF/SF inhibitors will be required for most cancers to achieve a cytotoxic tumor response." @default.
- W2016579969 created "2016-06-24" @default.
- W2016579969 creator A5026220299 @default.
- W2016579969 creator A5060130342 @default.
- W2016579969 date "2008-02-01" @default.
- W2016579969 modified "2023-10-16" @default.
- W2016579969 title "Showering c-MET-dependent cancers with drugs" @default.
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- W2016579969 doi "https://doi.org/10.1016/j.gde.2008.02.001" @default.
- W2016579969 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/18406132" @default.