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

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 br...

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Detalles Bibliográficos
Autores principales: Li, Hui, Li, Han-Han, Chen, Qian, Wang, Yu-Yang, Fan, Chang-Chang, Duan, Yuan-Yuan, Huang, You, Zhang, Hui-Min, Li, Jia-Peng, Zhang, Xiao-Yu, Xiang, Yuan, Gu, Chao-Jiang, Wang, Li, Liao, Xing-Hua, Zhang, Tong-Cun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cognizant Communication Corporation 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8790130/
https://www.ncbi.nlm.nih.gov/pubmed/34321149
http://dx.doi.org/10.3727/096504021X16274672547967
Descripción
Sumario: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.