DLC1 interaction with S100A10 mediates inhibition of in vitro cell invasion and tumorigenicity of lung cancer cells through a RhoGAP-independent mechanism - Wikidata - awgldk - TriplyDB

DLC1 interaction with S100A10 mediates inhibition of in vitro cell invasion and tumorigenicity of lung cancer cells through a RhoGAP-independent mechanism

DLC1 interaction with S100A10 mediates inhibition of in vitro cell invasion and tumorigenicity of lung cancer cells through a RhoGAP-independent mechanism

http://www.wikidata.org/entity/Q28387959

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Deleted in liver cancer-1 (DLC1): an emerging metastasis suppressor gene Angiogenin interacts with the plasminogen activation system at the cell surface of breast cancer cells to regulate plasmin formation and cell migration Cooperative antiproliferative effect of coordinated ectopic expression of DLC1 tumor suppressor protein and silencing of MYC oncogene expression in liver cancer cells: Therapeutic implications DLC1 interaction with α-catenin stabilizes adherens junctions and enhances DLC1 antioncogenic activity Role of DLC1 tumor suppressor gene and MYC oncogene in pathogenesis of human hepatocellular carcinoma: potential prospects for combined targeted therapeutics (review)Silencing of DLC1 upregulates PAI-1 expression and reduces migration in normal prostate cells Mass spectrometric identification of ancient proteins as potential molecular biomarkers for a 2000-year-old osteogenic sarcoma Forced expression of S100A10 reduces sensitivity to oxaliplatin in colorectal cancer cells Solution structure of the phosphotyrosine binding (PTB) domain of human tensin2 protein in complex with deleted in liver cancer 1 (DLC1) peptide reveals a novel peptide binding mode.Annexin A2 silencing induces G2 arrest of non-small cell lung cancer cells through p53-dependent and -independent mechanisms.Annexin A2 heterotetramer: structure and function Functions of S100 proteins.S100 protein family in human cancer.The biochemistry and regulation of S100A10: a multifunctional plasminogen receptor involved in oncogenesis.Joining S100 proteins and migration: for better or for worse, in sickness and in health.Regulation of deleted in liver cancer 1 tumor suppressor by protein-protein interactions and phosphorylation.GAP-independent functions of DLC1 in metastasis.Inhibition of cell migration and invasion mediated by the TAT-RasGAP317-326 peptide requires the DLC1 tumor suppressor.Loss of DLC1 is an independent prognostic factor in patients with oral squamous cell carcinoma.Deleted in liver cancer 1 expression and localization in hepatocellular carcinoma tissue sections.Integrative analysis of miRNA and mRNA paired expression profiling of primary fibroblast derived from diabetic foot ulcers reveals multiple impaired cellular functions.PKA-induced dimerization of the RhoGAP DLC1 promotes its inhibition of tumorigenesis and metastasis.Regulation of cell surface protease receptor S100A10 by retinoic acid therapy in acute promyelocytic leukemia (APL)

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P2860

DLC1 interaction with S100A10 mediates inhibition of in vitro cell invasion and tumorigenicity of lung cancer cells through a RhoGAP-independent mechanism

http://www.wikidata.org/entity/Q28387959

description

2011 nî lūn-bûn

@nan

2011 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի ապրիլին հրատարակված գիտական հոդված

@hy

2011年の論文

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2011年論文

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2011年論文

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2011年論文

@zh-hk

2011年論文

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2011年論文

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2011年论文

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name

DLC1 interaction with S100A10 ...... a RhoGAP-independent mechanism

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DLC1 interaction with S100A10 ...... a RhoGAP-independent mechanism

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DLC1 interaction with S100A10 ...... a RhoGAP-independent mechanism

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type

label

DLC1 interaction with S100A10 ...... a RhoGAP-independent mechanism

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DLC1 interaction with S100A10 ...... a RhoGAP-independent mechanism

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DLC1 interaction with S100A10 ...... a RhoGAP-independent mechanism

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prefLabel

DLC1 interaction with S100A10 ...... a RhoGAP-independent mechanism

@ast

DLC1 interaction with S100A10 ...... a RhoGAP-independent mechanism

@en

DLC1 interaction with S100A10 ...... a RhoGAP-independent mechanism

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P356

0008-5472.CAN-10-2158

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Cancer Research

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DLC1 interaction with S100A10 ...... a RhoGAP-independent mechanism

@en

P2093

Drazen B Zimonjic

http://www.w3.org/2001/XMLSchema#string

Nicholas C Popescu

http://www.w3.org/2001/XMLSchema#string

Xuyu Yang

http://www.w3.org/2001/XMLSchema#string

P2860

DLC-1: a Rho GTPase-activating protein and tumour suppressor

DLC-1, a GTPase-activating protein for Rho, is associated with cell proliferation, morphology, and migration in human hepatocellular carcinoma

DLC-1 suppresses non-small cell lung cancer growth and invasion by RhoGAP-dependent and independent mechanisms

Interaction of deleted in liver cancer 1 with tensin2 in caveolae and implications in tumor suppression

p120Ras-GAP binds the DLC1 Rho-GAP tumor suppressor protein and inhibits its RhoA GTPase and growth-suppressing activities

The SAM domain of the RhoGAP DLC1 binds EF1A1 to regulate cell migration

The phosphotyrosine-independent interaction of DLC-1 and the SH2 domain of cten regulates focal adhesion localization and growth suppression activity of DLC-1

Protein-protein recognition via short amphiphilic helices; a mutational analysis of the binding site of annexin II for p11

Endothelial cell annexin A2 regulates polyubiquitination and degradation of its binding partner S100A10/p11

Oncogenic inhibition by a deleted in liver cancer gene requires cooperation between tensin binding and Rho-specific GTPase-activating protein activities

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2916-25

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scholarly article

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10.1158/0008-5472.CAN-10-2158

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8

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71

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2011-04-15T00:00:00Z

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50270934

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21372205

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3078213

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