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c-MET as a potential therapeutic target and biomarker in cancer
by
Tsao, Ming-Sound
, Sierra, J. Rafael
in
Angiogenesis
/ Breast
/ c-Met protein
/ Cell activation
/ Cell proliferation
/ Colon
/ Head and neck carcinoma
/ Hepatocyte growth factor
/ Kidney cancer
/ Lung carcinoma
/ Non-small cell lung carcinoma
/ Pancreas
/ Pancreatic carcinoma
/ Protein-tyrosine kinase receptors
/ Reviews
/ Signal transduction
/ Small cell lung carcinoma
/ Therapeutic applications
/ Thyroid
2011
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c-MET as a potential therapeutic target and biomarker in cancer
by
Tsao, Ming-Sound
, Sierra, J. Rafael
in
Angiogenesis
/ Breast
/ c-Met protein
/ Cell activation
/ Cell proliferation
/ Colon
/ Head and neck carcinoma
/ Hepatocyte growth factor
/ Kidney cancer
/ Lung carcinoma
/ Non-small cell lung carcinoma
/ Pancreas
/ Pancreatic carcinoma
/ Protein-tyrosine kinase receptors
/ Reviews
/ Signal transduction
/ Small cell lung carcinoma
/ Therapeutic applications
/ Thyroid
2011
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Do you wish to request the book?
c-MET as a potential therapeutic target and biomarker in cancer
by
Tsao, Ming-Sound
, Sierra, J. Rafael
in
Angiogenesis
/ Breast
/ c-Met protein
/ Cell activation
/ Cell proliferation
/ Colon
/ Head and neck carcinoma
/ Hepatocyte growth factor
/ Kidney cancer
/ Lung carcinoma
/ Non-small cell lung carcinoma
/ Pancreas
/ Pancreatic carcinoma
/ Protein-tyrosine kinase receptors
/ Reviews
/ Signal transduction
/ Small cell lung carcinoma
/ Therapeutic applications
/ Thyroid
2011
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c-MET as a potential therapeutic target and biomarker in cancer
Journal Article
c-MET as a potential therapeutic target and biomarker in cancer
2011
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Overview
The receptor tyrosine kinase c-MET and its ligand, hepatocyte growth factor (HGF), regulate multiple cellular processes that stimulate cell proliferation, invasion and angiogenesis. This review provides an overview of the evidence to support c-MET or the HGF/c-MET signaling pathway as relevant targets for personalized cancer treatment based on high frequencies of c-MET and/or HGF overexpression, activation, amplification in non-small cell lung carcinoma (NSCLC), gastric, ovarian, pancreatic, thyroid, breast, head and neck, colon and kidney carcinomas. Additionally, the current knowledge of small molecule inhibitors (tivantinib [ARQ 197]), c-MET/HGF antibodies (rilotumumab and MetMAb) and mechanisms of resistance to c-MET-targeted therapies are discussed.
Publisher
SAGE Publications,Sage Publications Ltd,SAGE Publishing
Subject
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