The miR-17-92 cluster of microRNAs confers tumorigenicity by inhibiting oncogene-induced senescence - Wikidata - awgldk - TriplyDB

The miR-17-92 cluster of microRNAs confers tumorigenicity by inhibiting oncogene-induced senescence

The miR-17-92 cluster of microRNAs confers tumorigenicity by inhibiting oncogene-induced senescence

http://www.wikidata.org/entity/Q24617045

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New Concepts in Cancer Biomarkers: Circulating miRNAs in Liquid Biopsies Noncoding RNA control of cellular senescence The impact of cellular senescence in cancer therapy: is it true or not?MYC and the art of microRNA maintenance Noncoding RNAs in DNA repair and genome integrity Outside the coding genome, mammalian microRNAs confer structural and functional complexity Pigmy MicroRNA: surveillance cops in Therapies kingdom NKX2-5, a modifier of skeletal muscle pathology due to RNA toxicity.Methods to quantify microRNAs in the Myc gene network for posttranscriptional gene repression.MicroRNA 17-92 cluster mediates ETS1 and ETS2-dependent RAS-oncogenic transformation Deep sequencing reveals novel microRNAs and regulation of microRNA expression during cell senescence.The antileukemia activity of natural product HQ17(3) is possibly associated with downregulation of miR-17-92 cluster.Identification of miR-374a as a prognostic marker for survival in patients with early-stage nonsmall cell lung cancer.A set of miRNAs participates in the cellular senescence program in human diploid fibroblasts.miR-19a acts as an oncogenic microRNA and is up-regulated in bladder cancer Human neonatal cardiovascular progenitors: unlocking the secret to regenerative ability.Phosphorylation of Tip60 by p38α regulates p53-mediated PUMA induction and apoptosis in response to DNA damage Dependence of intracellular and exosomal microRNAs on viral E6/E7 oncogene expression in HPV-positive tumor cells.Novel microRNA prosurvival cocktail for improving engraftment and function of cardiac progenitor cell transplantation.MicroRNA-18a inhibits hypoxia-inducible factor 1α activity and lung metastasis in basal breast cancers miR-20a encoded by the miR-17-92 cluster increases the metastatic potential of osteosarcoma cells by regulating Fas expression.MicroRNAs and STAT interplay.MetastamiRs: non-coding MicroRNAs driving cancer invasion and metastasis Regulation of senescence by microRNA biogenesis factors MicroRNA-106a functions as an oncogene in human gastric cancer and contributes to proliferation and metastasis in vitro and in vivo.Functional interactions among members of the miR-17-92 cluster in lymphocyte development, differentiation and malignant transformation.Differential Sensitivity of Target Genes to Translational Repression by miR-17~92.Transfection of microRNA Mimics Should Be Used with Caution.Dysregulation of microRNAs in cancer.Diagnostic significance of miR-106a in gastric cancer.PDGF-B-mediated downregulation of miR-21: new insights into PDGF signaling in glioblastoma.MicroRNAs in age-related diseases.MicroRNA-15b regulates mitochondrial ROS production and the senescence-associated secretory phenotype through sirtuin 4/SIRT4 MicroRNA-17-92 cluster mediates the proliferation and survival of neural progenitor cells after stroke.The MicroRNA-17-92 cluster enhances axonal outgrowth in embryonic cortical neurons The Landscape of microRNA Targeting in Prostate Cancer Defined by AGO-PAR-CLIP.Adenomatous polyposis coli (APC) regulates miR17-92 cluster through β-catenin pathway in colorectal cancer.Regulation of miR-19 to breast cancer chemoresistance through targeting PTEN A component of the mir-17-92 polycistronic oncomir promotes oncogene-dependent apoptosis.Induction of p38δ expression plays an essential role in oncogenic ras-induced senescence

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The miR-17-92 cluster of microRNAs confers tumorigenicity by inhibiting oncogene-induced senescence

http://www.wikidata.org/entity/Q24617045

description

2010 nî lūn-bûn

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2010 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի նոյեմբերին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

The miR-17-92 cluster of micro ...... ng oncogene-induced senescence

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The miR-17-92 cluster of micro ...... ng oncogene-induced senescence

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The miR-17-92 cluster of micro ...... ng oncogene-induced senescence

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The miR-17-92 cluster of micro ...... ng oncogene-induced senescence

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The miR-17-92 cluster of micro ...... ng oncogene-induced senescence

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The miR-17-92 cluster of micro ...... ng oncogene-induced senescence

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prefLabel

The miR-17-92 cluster of micro ...... ng oncogene-induced senescence

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The miR-17-92 cluster of micro ...... ng oncogene-induced senescence

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0008-5472.CAN-10-1938

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Cancer Research

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The miR-17-92 cluster of micro ...... ng oncogene-induced senescence

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Changchuan Xie

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Changchun Xiao

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Jiahuai Han

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Lixin Hong

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Peiqing Sun

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Rong Liao

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Wen-Yuan Hu

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Young Jun Kang

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P2860

PRAK is essential for ras-induced senescence and tumor suppression

Oncogenic ras provokes premature cell senescence associated with accumulation of p53 and p16INK4a

A microRNA expression signature of human solid tumors defines cancer gene targets

MicroRNAs: target recognition and regulatory functions

Targeted deletion reveals essential and overlapping functions of the miR-17 through 92 family of miRNA clusters

miRiad roles for the miR-17-92 cluster in development and disease

Lymphoproliferative disease and autoimmunity in mice with increased miR-17-92 expression in lymphocytes

Genetic dissection of the miR-17~92 cluster of microRNAs in Myc-induced B-cell lymphomas

miR-19 is a key oncogenic component of mir-17-92

Crucial role of p53-dependent cellular senescence in suppression of Pten-deficient tumorigenesis

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8547-8557

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21

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