SIRT1 induces EMT by cooperating with EMT transcription factors and enhances prostate cancer cell migration and metastasis. - Wikidata - wikimedia - TriplyDB

SIRT1 induces EMT by cooperating with EMT transcription factors and enhances prostate cancer cell migration and metastasis.

SIRT1 induces EMT by cooperating with EMT transcription factors and enhances prostate cancer cell migration and metastasis.

http://www.wikidata.org/entity/Q34149920

about

Sirtuins and Cancer: Role in the Epithelial-Mesenchymal Transition MicroRNA Regulation of Epithelial to Mesenchymal Transition Transcriptional control of cancer metastasis Epigenetic plasticity: a central regulator of epithelial-to-mesenchymal transition in cancer Sirtuins in epigenetic regulation High SIRT1 expression is a negative prognosticator in pancreatic ductal adenocarcinoma Regulation of epithelial-mesenchymal transition through epigenetic and post-translational modifications Epigenetic determinants of metastasis The sirtuins promote Dishevelled-1 scaffolding of TIAM1, Rac activation and cell migration Plumbagin elicits differential proteomic responses mainly involving cell cycle, apoptosis, autophagy, and epithelial-to-mesenchymal transition pathways in human prostate cancer PC-3 and DU145 cells Alisertib induces cell cycle arrest and autophagy and suppresses epithelial-to-mesenchymal transition involving PI3K/Akt/mTOR and sirtuin 1-mediated signaling pathways in human pancreatic cancer cells Causes of genome instability: the effect of low dose chemical exposures in modern society Pro-apoptotic and pro-autophagic effects of the Aurora kinase A inhibitor alisertib (MLN8237) on human osteosarcoma U-2 OS and MG-63 cells through the activation of mitochondria-mediated pathway and inhibition of p38 MAPK/PI3K/Akt/mTOR signaling pat Emerging Roles of SIRT1 in Cancer Drug Resistance Sirt1-deficient mice have hypogonadotropic hypogonadism due to defective GnRH neuronal migration.GSK3β controls epithelial-mesenchymal transition and tumor metastasis by CHIP-mediated degradation of Slug DACH1 inhibits SNAI1-mediated epithelial-mesenchymal transition and represses breast carcinoma metastasis.Frizzled 7 expression is positively regulated by SIRT1 and β-catenin in breast cancer cells.Epigenetic regulation of epithelial-mesenchymal transition NUBPL, a novel metastasis-related gene, promotes colorectal carcinoma cell motility by inducing epithelial-mesenchymal transition.IBP regulates epithelial-to-mesenchymal transition and the motility of breast cancer cells via Rac1, RhoA and Cdc42 signaling pathways.ATM-mediated stabilization of ZEB1 promotes DNA damage response and radioresistance through CHK1.Identification of a novel polyprenylated acylphloroglucinol‑derived SIRT1 inhibitor with cancer‑specific anti-proliferative and invasion-suppressing activities.The role of epithelial plasticity in prostate cancer dissemination and treatment resistance Role of SIRT1 in regulation of epithelial-to-mesenchymal transition in oral squamous cell carcinoma metastasis Loss of Sirt1 promotes prostatic intraepithelial neoplasia, reduces mitophagy, and delays PARK2 translocation to mitochondria TACC3 is essential for EGF-mediated EMT in cervical cancer Sorting out functions of sirtuins in cancer SIRT1 inactivation evokes antitumor activities in NSCLC through the tumor suppressor p27.SIRT1 is highly expressed in brain metastasis tissues of non-small cell lung cancer (NSCLC) and in positive regulation of NSCLC cell migration.The expression and correlation of SIRT1 and Phospho-SIRT1 in colorectal cancer.Trim28 contributes to EMT via regulation of E-cadherin and N-cadherin in lung cancer cell lines.Overexpression of SIRT1 promotes metastasis through epithelial-mesenchymal transition in hepatocellular carcinoma.SIRT7 inactivation reverses metastatic phenotypes in epithelial and mesenchymal tumors The androgen receptor plays a suppressive role in epithelial- mesenchymal transition of human prostate cancer stem progenitor cells Downregulation of dystroglycan glycosyltransferases LARGE2 and ISPD associate with increased mortality in clear cell renal cell carcinoma.The Histone Deacetylase Sirtuin 1 Is Reduced in Systemic Sclerosis and Abrogates Fibrotic Responses by Targeting Transforming Growth Factor β Signaling.Loss of miR-449a in ERG-associated prostate cancer promotes the invasive phenotype by inducing SIRT1.Prognostic and clinical value of Sirt1 expression in gastric cancer: A systematic meta-analysis.miR-199a-5p suppresses human bladder cancer cell metastasis by targeting CCR7.

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SIRT1 induces EMT by cooperating with EMT transcription factors and enhances prostate cancer cell migration and metastasis.

http://www.wikidata.org/entity/Q34149920

description

2012 nî lūn-bûn

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2012 թուականի Յունուարին հրատարակուած գիտական յօդուած

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2012 թվականի հունվարին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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name

SIRT1 induces EMT by cooperati ...... cell migration and metastasis.

@ast

SIRT1 induces EMT by cooperati ...... cell migration and metastasis.

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SIRT1 induces EMT by cooperati ...... cell migration and metastasis.

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type

label

SIRT1 induces EMT by cooperati ...... cell migration and metastasis.

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SIRT1 induces EMT by cooperati ...... cell migration and metastasis.

@en

SIRT1 induces EMT by cooperati ...... cell migration and metastasis.

@nl

prefLabel

SIRT1 induces EMT by cooperati ...... cell migration and metastasis.

@ast

SIRT1 induces EMT by cooperati ...... cell migration and metastasis.

@en

SIRT1 induces EMT by cooperati ...... cell migration and metastasis.

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SIRT1 induces EMT by cooperati ...... cell migration and metastasis

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D V Faller

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

J D Lovaas

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

J Wang

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

L K Chmilewski

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

L Zhu

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

V Byles

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P2860

The SLUG zinc-finger protein represses E-cadherin in breast cancer

Sirtuin functions in health and disease

Sirtuin 1 is required for antagonist-induced transcriptional repression of androgen-responsive genes by the androgen receptor

ZEB1 represses E-cadherin and induces an EMT by recruiting the SWI/SNF chromatin-remodeling protein BRG1

Prohibitin and the SWI/SNF ATPase subunit BRG1 are required for effective androgen antagonist-mediated transcriptional repression of androgen receptor-regulated genes

SIP1/ZEB2 induces EMT by repressing genes of different epithelial cell-cell junctions

DeltaEF1 is a transcriptional repressor of E-cadherin and regulates epithelial plasticity in breast cancer cells

Complex networks orchestrate epithelial-mesenchymal transitions

Snail, Zeb and bHLH factors in tumour progression: an alliance against the epithelial phenotype?

Epithelial-mesenchymal transitions in development and pathologies

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10.1038/ONC.2011.612

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43

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31

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