MicroRNA-130a-3p suppresses cell migration and invasion by inhibition of TBL1XR1-mediated EMT in human gastric carcinoma. (Q47677452)

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8 April 2020

title

MicroRNA-130a-3p suppresses cell migration and invasion by inhibition of TBL1XR1-mediated EMT in human gastric carcinoma (English)

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8 April 2020

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6

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Jiafu Ji

8

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author name string

Shanshan Wang

1

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Haibo Han

2

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Ying Hu

3

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Wei Yang

4

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Yunwei Lv

5

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Lianhai Zhang

7

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publication date

19 November 2017

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published in

Molecular Carcinogenesis

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volume

57

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issue

3

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page(s)

383-392

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Gastric cancer: a primer on the epidemiology and biology of the disease and an overview of the medical management of advanced disease

8 April 2020

cites work

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MiR-130a, miR-203 and miR-205 jointly repress key oncogenic pathways and are downregulated in prostate carcinoma

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Onco-miR-130 promotes cell proliferation and migration by targeting TGFβR2 in gastric cancer

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Rufy3 promotes metastasis through epithelial-mesenchymal transition in colorectal cancer

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TBLR1 is a novel prognostic marker and promotes epithelial-mesenchymal transition in cervical cancer.

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Transducin (β)-like 1 X-linked receptor 1 promotes gastric cancer progression via the ERK1/2 pathway

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MiR-130a-3p regulates cell migration and invasion via inhibition of Smad4 in gemcitabine resistant hepatoma cells

21 January 2018

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Epigenetic disruption of miR-130a promotes prostate cancer by targeting SEC23B and DEPDC1.

21 January 2018

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ADAM23 is downregulated in side population and suppresses lung metastasis of lung carcinoma cells

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Developmental and functional expression of miRNA-stability related genes in the nervous system

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Role of miRNAs and their potential to be useful as diagnostic and prognostic biomarkers in gastric cancer

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Mathematical modeling of combinatorial regulation suggests that apparent positive regulation of targets by miRNA could be an artifact resulting from competition for mRNA

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A corepressor/coactivator exchange complex required for transcriptional activation by nuclear receptors and other regulated transcription factors

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Identifiers

DOI

10.1002/MC.22762

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