High level of miR-21, miR-10b, and miR-31 expression in bilateral vs. unilateral breast carcinomas. (Q46935119)

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16 January 2020

title

High level of miR-21, miR-10b, and miR-31 expression in bilateral vs. unilateral breast carcinomas (English)

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16 January 2020

2

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Natalia Mitiushkina

3

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16 January 2020

Aleksandr Togo

4

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author name string

Aglaya G Iyevleva

1

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16 January 2020

Yoshio Miki

5

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16 January 2020

Evgeny N Imyanitov

6

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language of work or name

English

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publication date

5 November 2011

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Breast Cancer Research and Treatment

16 January 2020

published in

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16 January 2020

volume

131

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issue

3

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16 January 2020

page(s)

1049-1059

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https://scigraph.springernature.com/pub.10.1007/s10549-011-1845-z

16 January 2020

exact match

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Knockdown of miR-21 in human breast cancer cell lines inhibits proliferation, in vitro migration and in vivo tumor growth

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Tumour invasion and metastasis initiated by microRNA-10b in breast cancer

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miR-10b targets Tiam1: implications for Rac activation and carcinoma migration

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Onco-miR-155 targets SHIP1 to promote TNFalpha-dependent growth of B cell lymphomas

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MicroRNA-155 functions as an OncomiR in breast cancer by targeting the suppressor of cytokine signaling 1 gene

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MicroRNA-155 regulates cell survival, growth, and chemosensitivity by targeting FOXO3a in breast cancer

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Targeting of SMAD5 links microRNA-155 to the TGF-beta pathway and lymphomagenesis

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Inducible microRNA-155 feedback promotes type I IFN signaling in antiviral innate immunity by targeting suppressor of cytokine signaling 1.

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The oncogenic microRNA-27a targets genes that regulate specificity protein transcription factors and the G2-M checkpoint in MDA-MB-231 breast cancer cells.

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MicroRNA-27a Indirectly Regulates Estrogen Receptor {alpha} Expression and Hormone Responsiveness in MCF-7 Breast Cancer Cells

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miR-27a regulates the growth, colony formation and migration of pancreatic cancer cells by targeting Sprouty2.

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The role of miR-31 and its target gene SATB2 in cancer-associated fibroblasts.

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MicroRNA-200c mitigates invasiveness and restores sensitivity to microtubule-targeting chemotherapeutic agents

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21 January 2018

Identifiers

DOI

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16 January 2020

1 reference