Antitumor activity and pharmacology of a selective focal adhesion kinase inhibitor, PF-562,271
about
Actomyosin-mediated cellular tension drives increased tissue stiffness and β-catenin activation to induce epidermal hyperplasia and tumor growthFAK and paxillin, two potential targets in pancreatic cancerNuclear FAK: a new mode of gene regulation from cellular adhesionsFAK in cancer: mechanistic findings and clinical applicationsAltering FAK-paxillin interactions reduces adhesion, migration and invasion processesCrystal Structures of the FAK Kinase in Complex with TAE226 and Related Bis-Anilino Pyrimidine Inhibitors Reveal a Helical DFG ConformationFocal Adhesion Kinase Inhibitors in Combination with Erlotinib Demonstrate Enhanced Anti-Tumor Activity in Non-Small Cell Lung CancerIntegrin-matrix clusters form podosome-like adhesions in the absence of traction forcesMyosin II activity regulates vinculin recruitment to focal adhesions through FAK-mediated paxillin phosphorylation.Activation of focal adhesion kinase through an interaction with β4 integrin contributes to tumorigenicity of colon cancerEvolving Therapies and FAK Inhibitors for the Treatment of CancerAdhesion to fibronectin regulates Hippo signaling via the FAK-Src-PI3K pathway.Cooperation between c-Met and focal adhesion kinase family members in medulloblastoma and implications for therapy.Inhibition of focal adhesion kinase by PF-562,271 inhibits the growth and metastasis of pancreatic cancer concomitant with altering the tumor microenvironment.Myosin IIA/IIB restrict adhesive and protrusive signaling to generate front-back polarity in migrating cellsDifferential requirement for focal adhesion kinase signaling in cancer progression in the transgenic adenocarcinoma of mouse prostate modelFocal adhesion kinase and endothelial cell apoptosis.Regulation of focal adhesion turnover by ErbB signalling in invasive breast cancer cells.Knock-in mutation reveals an essential role for focal adhesion kinase activity in blood vessel morphogenesis and cell motility-polarity but not cell proliferation.Down-regulation of epithelial cadherin is required to initiate metastatic outgrowth of breast cancer.Molecular and cellular impact of Psoriasin (S100A7) on the healing of human wounds.Inhibiting the interaction of cMET and IGF-1R with FAK effectively reduces growth of pancreatic cancer cells in vitro and in vivoGrowth activation alone is not sufficient to cause metastatic thyroid cancer in a mouse model of follicular thyroid carcinomaAnalyses of merlin/NF2 connection to FAK inhibitor responsiveness in serous ovarian cancerInhibition of focal adhesion kinase decreases tumor growth in human neuroblastomaFocal adhesion kinase: an alternative focus for anti-angiogenesis therapy in ovarian cancer.Role of kinase-independent and -dependent functions of FAK in endothelial cell survival and barrier function during embryonic development.Adrenergic signaling regulates mitochondrial Ca2+ uptake through Pyk2-dependent tyrosine phosphorylation of the mitochondrial Ca2+ uniporterHeat shock protein 90β stabilizes focal adhesion kinase and enhances cell migration and invasion in breast cancer cellsFAK 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.PND-1186 FAK inhibitor selectively promotes tumor cell apoptosis in three-dimensional environments.FAK deletion promotes p53-mediated induction of p21, DNA-damage responses and radio-resistance in advanced squamous cancer cells.Targeting Pyk2 for therapeutic interventionMerlin deficiency predicts FAK inhibitor sensitivity: a synthetic lethal relationshipFocal adhesion kinase is required for synovial fibroblast invasion, but not murine inflammatory arthritisPyk2 promotes tumor progression in multiple myelomaNuclear FAK controls chemokine transcription, Tregs, and evasion of anti-tumor immunity.Role for NUP62 depletion and PYK2 redistribution in dendritic retraction resulting from chronic stressTailoring tyrosine kinase inhibitors to fit the lung cancer genome.
P2860
Q24613142-F7A628D9-5807-4C9B-ACBF-25AAF2108A4BQ26765360-3A07C5C8-4B00-43C6-8D36-FCADC29E0A35Q26864184-EC7F9422-D4B3-45F5-AE93-88BCE234FA47Q27026533-40728330-F639-423E-9928-6838A4B1EDB4Q27314883-1B3776C8-F2E1-4C9F-860B-C23E24E1B61FQ27652985-F303939D-61F3-4E28-820E-5396806B36B6Q28550689-855F6BF8-3DB9-48E3-80B6-77B7349D82F4Q28568664-79FB112D-3A6B-44C9-974D-58E2B324FAF4Q28586815-4EEFF155-D120-4097-AF01-D98D01FC6382Q28771754-0E90FDAE-30DD-4761-BB0E-DEC204E93220Q28972291-56AE827F-BD44-4707-B74F-953E0562CC4CQ30278951-6A9D2907-85BD-456B-B104-FC3988BE2D61Q30422676-DE64D50B-D013-44FD-A90A-F040601D6028Q30424344-5ABF3C15-53F0-4201-8213-98793832653EQ30430251-0F69F659-4817-4E67-84BB-DE0EB436ECA5Q30435351-04B06548-6C80-48FC-8A88-92A6E53F745DQ30459602-EF6F03BF-528B-40A8-B5DF-23EBE274B897Q30486408-91AA2DB7-857D-4A4E-A223-4F23A2F314D6Q30495320-27900C80-39CC-4451-9C1D-F33441F5D40CQ30502431-A2931BA6-8892-4F86-88CA-790FC9407E4CQ33724031-BA0775E9-BEA1-4C52-A6B7-4B158694FB30Q33737191-0E1F29AD-A1D3-47F1-A9E8-6F7C67F9B932Q33775577-FE1E6249-5463-465C-8576-747255E277C7Q33787214-B5F92023-0819-4C0E-8D1E-D7348D268E74Q33794045-9FC0B09C-1901-498D-AC5B-A73653762956Q33911213-87AA19E7-7871-4EAC-810D-6D490092A3DFQ33916059-C7A8C5A8-7887-4F34-935B-2C81E1B822BDQ33974822-ECA31228-A138-460B-8DA4-C754C557797FQ33998634-F2AF7EEF-D645-4C6D-A5FB-370BFFD5518CQ34021043-E0AAE48C-DEDE-43CC-8064-4CE164EAABA6Q34103876-779A7FAA-6261-4796-977E-685A470ECB58Q34103928-816CB375-DC56-41F2-9811-DA75599E3C79Q34109901-AF6A6E27-7E59-4F0B-AB58-2D9AB28CBFF4Q34146883-A71CA0C1-C1A0-4B92-8235-9E604A614618Q34193347-83FA9ADC-013D-4E87-AD46-A25F5508C341Q34374676-CAD6AAC0-7D25-4C63-912A-843148A79787Q34398382-189DFDF9-A43D-40D3-BFD0-FDB17BDB6A07Q34495723-E163FCF6-6B51-42DF-B51F-D3FAFEE1E8A0Q34525933-F3D2CEBF-D3A0-4CFD-B546-F4EDE2D74C3BQ34754045-E07D0ADC-91EB-4976-A6A7-BE08AB4C1EA3
P2860
Antitumor activity and pharmacology of a selective focal adhesion kinase inhibitor, PF-562,271
description
2008 nî lūn-bûn
@nan
2008 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի մարտին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Antitumor activity and pharmac ...... n kinase inhibitor, PF-562,271
@ast
Antitumor activity and pharmac ...... n kinase inhibitor, PF-562,271
@en
Antitumor activity and pharmac ...... n kinase inhibitor, PF-562,271
@nl
type
label
Antitumor activity and pharmac ...... n kinase inhibitor, PF-562,271
@ast
Antitumor activity and pharmac ...... n kinase inhibitor, PF-562,271
@en
Antitumor activity and pharmac ...... n kinase inhibitor, PF-562,271
@nl
prefLabel
Antitumor activity and pharmac ...... n kinase inhibitor, PF-562,271
@ast
Antitumor activity and pharmac ...... n kinase inhibitor, PF-562,271
@en
Antitumor activity and pharmac ...... n kinase inhibitor, PF-562,271
@nl
P2093
P3181
P1433
P1476
Antitumor activity and pharmac ...... n kinase inhibitor, PF-562,271
@en
P2093
Beth Cooper
Catherine Hulford
Christofer Autry
Daniel Richter
Earling Emerson
Erika Schmitt
Felix Vajdos
P304
P3181
P356
10.1158/0008-5472.CAN-07-5155
P407
P577
2008-03-15T00:00:00Z