4.4 Article

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

Journal

ONCOLOGY RESEARCH
Volume 28, Issue 9, Pages 885-897

Publisher

TECH SCIENCE PRESS
DOI: 10.3727/096504021X16274672547967

Keywords

DNMT1; Maspin; miR-142-5p; MKL-1; Breast cancer

Categories

Funding

  1. Natural Science Foundation of Hubei Province [2018CFB369]
  2. China Postdoctoral Science Foundation [2018M632927]
  3. Applied Basic Research Project of Wuhan City [2017060201010193]
  4. Hubei Provincial Plan of Natural Science Foundation of China [ZRMS2019000926]

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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-1's 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.

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