miR-142-5p Inhibits Cell Invasion and Migration by Targeting DNMT1 in Breast Cancer

Author:

Li Hui1,Li Han-Han2,Chen Qian3,Wang Yu-Yang3,Fan Chang-Chang3,Duan Yuan-Yuan3,Huang You3,Zhang Hui-Min3,Li Jia-Peng3,Zhang Xiao-Yu3,Xiang Yuan3,Gu Chao-Jiang3,Wang Li4,Liao Xing-Hua3,Zhang Tong-Cun3

Affiliation:

1. Department of Hematology and Nephrology, Tianyou Hospital Affiliated to Wuhan University of Science and TechnologyHubeiP.R. China

2. Nanjing Vazyme Biotech Co. Ltd.NanjingP.R. China

3. College of Life Sciences and Health, Wuhan University of Science and TechnologyHubeiP.R. China

4. School of Resource and Environmental Engineering, Wuhan University of Science and TechnologyHubeiP.R. China

Abstract

Abnormal cell proliferation caused by abnormal transcription regulation mechanism seems to be one of the reasons for the progression of breast cancer and also the pathological basis. MicroRNA-142-5p (miR-142-5p) is a low-expressed miRNA in breast cancer. The role of MKL-1s regulation of DNMT1 in breast cancer cell proliferation and migration is still unclear. MKL-1 (myocardin related transcription factor A) can bind to the conserved cis-regulatory element CC (A/T) 6GG (called CarG box) in the promoter to regulate the transcription of miR-142-5p. The expressions of miR-142-5p and MKL-1 are positively correlated. In addition, it has been proved that DNMT1 is the target of miR-142-5p, which inhibits the expression of DNMT1 by targeting the 3-UTR of DNMT1, thereby forming a feedback loop and inhibiting the migration and proliferation of breast cancer. Our data provide important and novel insights into the MKL-1/miR-142-5p/DNMT1/maspin signaling pathway and may become a new idea for breast cancer diagnosis, treatment, and prognosis.

Publisher

Cognizant, LLC

Subject

Cancer Research,Oncology,General Medicine

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