PND-1186 FAK inhibitor selectively promotes tumor cell apoptosis in three-dimensional environments.
about
FAK in cancer: mechanistic findings and clinical applicationsEvolving Therapies and FAK Inhibitors for the Treatment of CancerN-WASP-directed actin polymerization activates Cas phosphorylation and lamellipodium spreading.Knock-in mutation reveals an essential role for focal adhesion kinase activity in blood vessel morphogenesis and cell motility-polarity but not cell proliferation.Analyses of merlin/NF2 connection to FAK inhibitor responsiveness in serous ovarian cancerFAK Inhibition disrupts a β5 integrin signaling axis controlling anchorage-independent ovarian carcinoma growth.Oral delivery of PND-1186 FAK inhibitor decreases tumor growth and spontaneous breast to lung metastasis in pre-clinical models.Merlin deficiency predicts FAK inhibitor sensitivity: a synthetic lethal relationshipPyk2 promotes tumor progression in multiple myelomaUnderstanding the roles of FAK in cancer: inhibitors, genetic models, and new insightsFAK activity protects nucleostemin in facilitating breast cancer spheroid and tumor growthTarget modulation by a kinase inhibitor engineered to induce a tandem blockade of the epidermal growth factor receptor (EGFR) and c-Src: the concept of type III combi-targetingProstaglandins in cancer cell adhesion, migration, and invasionNuclear-localized focal adhesion kinase regulates inflammatory VCAM-1 expression.Focal Adhesion Kinase: Insight into Molecular Roles and Functions in Hepatocellular CarcinomaFocal adhesion kinase contributes to proliferative potential of ErbB2 mammary tumour cells but is dispensable for ErbB2 mammary tumour induction in vivoModulation of FAK and Src adhesion signaling occurs independently of adhesion complex composition.Pharmacologic blockade of FAK autophosphorylation decreases human glioblastoma tumor growth and synergizes with temozolomide.Inhibition of focal adhesion kinase (FAK) activity prevents anchorage-independent ovarian carcinoma cell growth and tumor progression.Mitoxantrone targets the ATP-binding site of FAK, binds the FAK kinase domain and decreases FAK, Pyk-2, c-Src, and IGF-1R in vitro kinase activitiesSynergism of FAK and tyrosine kinase inhibition in Ph+ B-ALL.Targeting the p53 pathway.A non-canonical role for Rgnef in promoting integrin-stimulated focal adhesion kinase activation.Focal adhesion kinase autophosphorylation inhibition decreases colon cancer cell growth and enhances the efficacy of chemotherapy.Inhibition of endothelial FAK activity prevents tumor metastasis by enhancing barrier function.Targeted inhibition of Src kinase with dasatinib blocks thyroid cancer growth and metastasis.Stromal Modulators of TGF-β in Cancer.Kinase inhibitors as potential agents in the treatment of multiple myeloma.Ambivalent role of pFAK-Y397 in serous ovarian cancer--a study of the OVCAD consortium.Focal adhesion kinase as a cancer therapy target.Influence of stress on extracellular matrix and integrin biology.Targeting FAK in human cancer: from finding to first clinical trials.RhoGEFs in cell motility: novel links between Rgnef and focal adhesion kinase.Meaningful prevention of breast cancer metastasis: candidate therapeutics, preclinical validation, and clinical trial concerns.Initial testing of VS-4718, a novel inhibitor of focal adhesion kinase (FAK), against pediatric tumor models by the Pediatric Preclinical Testing Program.Oncogenic Receptor Tyrosine Kinases Directly Phosphorylate Focal Adhesion Kinase (FAK) as a Resistance Mechanism to FAK-Kinase Inhibitors.Deciphering the effect of an oxovanadium(iv) complex with the flavonoid chrysin (VOChrys) on intracellular cell signalling pathways in an osteosarcoma cell line.Molecular Pathways: Endothelial Cell FAK-A Target for Cancer Treatment.Multiplexed high content screening reveals that cigarette smoke condensate-altered cell signaling pathways are accentuated through FAK inhibition in human bronchial cells.Angiogenesis biomarkers and their targeting ligands as potential targets for tumor angiogenesis.
P2860
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P2860
PND-1186 FAK inhibitor selectively promotes tumor cell apoptosis in three-dimensional environments.
description
2010 nî lūn-bûn
@nan
2010 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
PND-1186 FAK inhibitor selecti ...... hree-dimensional environments.
@ast
PND-1186 FAK inhibitor selecti ...... hree-dimensional environments.
@en
PND-1186 FAK inhibitor selecti ...... hree-dimensional environments.
@nl
type
label
PND-1186 FAK inhibitor selecti ...... hree-dimensional environments.
@ast
PND-1186 FAK inhibitor selecti ...... hree-dimensional environments.
@en
PND-1186 FAK inhibitor selecti ...... hree-dimensional environments.
@nl
prefLabel
PND-1186 FAK inhibitor selecti ...... hree-dimensional environments.
@ast
PND-1186 FAK inhibitor selecti ...... hree-dimensional environments.
@en
PND-1186 FAK inhibitor selecti ...... hree-dimensional environments.
@nl
P2093
P2860
P356
P1476
PND-1186 FAK inhibitor selecti ...... three-dimensional environments
@en
P2093
Ainhoa Mielgo
Alok Tomar
Cheni Kwok
Colin Walsh
Congxin Liang
Connie Sun
David D Schlaepfer
Dwayne G Stupack
Gerald McMahon
Isabelle Tanjoni
P2860
P304
P356
10.4161/CBT.9.10.11434
P577
2010-05-01T00:00:00Z