Search Results - "Yemma, Michael"
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MiR-138 and MiR-135 directly target focal adhesion kinase, inhibit cell invasion, and increase sensitivity to chemotherapy in cancer cells
Published in Anti-cancer agents in medicinal chemistry (01-01-2014)“…Focal Adhesion Kinase is a 125 kDa non-receptor kinase and overexpressed in many types of tumors. Recently, short noncoding RNAs, called microRNAs have been…”
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Pharmacologic blockade of FAK autophosphorylation decreases human glioblastoma tumor growth and synergizes with temozolomide
Published in Molecular cancer therapeutics (01-02-2013)“…Malignant gliomas are characterized by aggressive tumor growth with a mean survival of 15 to 18 months and frequently developed resistance to temozolomide…”
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Abstract C211: Demonstration of the efficacy of compound CFAK-C4, Targeting FAK-VEGFR-3 protein-protein interaction in animal models of gastric cancer
Published in Molecular cancer therapeutics (01-11-2013)“…While the emerging data strongly suggests that FAK is an excellent target for developmental therapeutics of cancer, small molecule kinase inhibitors of FAK…”
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A small molecule focal adhesion kinase (FAK) inhibitor, targeting Y397 site: 1-(2-hydroxyethyl) -3, 5, 7-triaza-1-azoniatricyclo [3.3.1.13,7]decane; bromide effectively inhibits FAK autophosphorylation activity and decreases cancer cell viability, clonogenicity and tumor growth in vivo
Published in Carcinogenesis (New York) (01-05-2012)“…Focal adhesion kinase (FAK) is a protein tyrosine kinase that is overexpressed in most solid types of tumors and plays an important role in the survival…”
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A FAK scaffold inhibitor disrupts FAK and VEGFR-3 signaling and blocks melanoma growth by targeting both tumor and endothelial cells
Published in Cell cycle (Georgetown, Tex.) (18-08-2014)“…Melanoma has the highest mortality rate of all skin cancers and a major cause of treatment failure is drug resistance. Tumors heterogeneity requires novel…”
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Targeting the C-terminal focal adhesion kinase scaffold in pancreatic cancer
Published in Cancer letters (28-10-2014)“…Highlights • C-terminal FAK scaffold inhibitor C10 selectively targets cancer cells with high FAK-Y925 and VEGFR3 expression levels. • FAK inhibitor C10…”
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Demonstration of the efficacy of compound CFAK-C4 targeting FAK-VEGFR3 protein-protein interaction in gastric cancer
Published in Journal of clinical oncology (20-05-2013)“…Abstract only e22143 Background: While the emerging data strongly suggest that FAK is an excellent target for developmental therapeutics of cancer, kinase…”
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The FAK scaffold inhibitor C4 disrupts FAK-VEGFR-3 signaling and inhibits pancreatic cancer growth
Published in Oncotarget (01-10-2013)“…Even with successful surgical resection and perioperative chemotherapy and radiation, pancreatic ductal adenocarcinoma (PDA) has a high incidence of…”
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Abstract B3: Anti-angiogenic properties of FAK-VEGFR3 scaffold inhibitors, C9 and C10
Published in Molecular cancer therapeutics (01-11-2013)“…Introduction: Focal adhesion kinase (FAK) and vascular endothelial growth factor receptor 3 (VEGFR3) are tyrosine kinases, which function as key modulators of…”
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Abstract A293: Novel allosteric small molecule FAK inhibitors effectively inhibit cancer cell viability and clonogenicity
Published in Molecular cancer therapeutics (01-11-2013)“…Introduction: Focal Adhesion Kinase is overexpressed and activated in many types of tumors and plays an important role in survival. Recently, we developed FAK…”
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Abstract 3247: Novel small molecule inhibitors C9 and C10 specifically disrupt the FAK-VEGFR3 signaling axis in cancer cells
Published in Cancer research (Chicago, Ill.) (15-04-2013)“…Introduction: FAK functions as both, a critical signaling kinase and a scaffolding protein to collectively mediate proliferation, survival, cell adhesion and…”
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Abstract 3756: Structure activity relationship studies of novel FAK inhibitor C4
Published in Cancer research (Chicago, Ill.) (15-04-2012)“…Introduction: FAK and VEGFR3 have stirred considerable interest in recent years as attractive anti-cancer targets, owing to their high expression across…”
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Pharmacological blockade of FAK autophosphorylation decreases human glioblastoma tumor growth and synergizes with temozolomide
Published in Molecular cancer therapeutics (12-12-2012)“…Malignant gliomas are characterized by aggressive tumor growth with a mean survival of 15–18 months and frequently developed resistance to temozolomide…”
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Abstract C191: Preclinical investigation of the antitumor efficacy in lung cancer of Y15, a novel focal adhesion kinase inhibitor
Published in Molecular cancer therapeutics (12-11-2011)“…Introduction: Focal adhesion kinase (FAK) is a nonreceptor tyrosine kinase that associates with a number of cell adhesion components, such as integrins,…”
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Abstract B244: The small molecule focal adhesion kinase inhibitor Y15 decreases human glioblastoma cell viability, clonogenicity, and tumor growth
Published in Molecular cancer therapeutics (12-11-2011)“…Introduction: Glioblastomas are the third most frequent cause of cancer-associated deaths due to the cancer cell rapid growth and high invasion and novel…”
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Abstract C124: Development of novel FAK inhibitors targeting the FAK-VEGFR3 protein-protein interaction site
Published in Molecular cancer therapeutics (12-11-2011)“…Introduction: FAK and VEGFR-3 have stirred considerable interest in recent years as attractive anti-cancer targets, owing to their high expression across…”
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