Journal of Southern Medical University ›› 2024, Vol. 44 ›› Issue (9): 1677-1684.doi: 10.12122/j.issn.1673-4254.2024.09.07

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MiR-6838-5p overexpression inhibits proliferation of breast cancer MCF-7 cells by downregulating DDR1 expression

Liangjun XUE1(), Qiuyu TAN2, Jingwen XU2, Lu FENG2, Wenjin LI2, Liang YAN2, Yulei LI2()   

  1. 1.Department of Radiotherapy, First Affiliated Hospital of Wannan Medical College, Wuhu 241002, China
    2.School of Basic Medicine, Wannan Medical College, Wuhu 241002, China
  • Received:2024-05-20 Online:2024-09-20 Published:2024-09-30
  • Contact: Yulei LI E-mail:xuelj016@163.com;liyulei@wnmc.edu.cn

Abstract:

Objective To explore the regulatory effect of miR-6838-5p on DDR1 gene expression and proliferation of breast cancer cells. Methods The expression levels of miR-6838-5p in normal breast epithelial cells and breast cancer cells were detected using qRT-PCR, and the potential target genes of miR-6838-5p was predicted using TargetscanV 8.0. Double luciferase reporter gene experiment was performed to verify the binding between miR-6838-5p and DDR1. Breast cancer MCF-7 cells were transfected via liposome, miR-6838-5p mimic, miR-6838-5p inhibitor, DDR1 siRNA, DDR1-overexpresisng vector, or both miR-6838-5p mimic and DDR1-overexpressing vector, and the changes in cell proliferation were examined with CCK-8 and EdU assays; Western blotting was used to detect the expression of DDR1. The mediating role of DDR1 in miR-6838-5p overexpression-induced inhibition of MCF-7 cell proliferation was verified in a nude mouse model bearing MCF-7 cell xenografts. Results The expression of miR-6838-5p was significantly lower in breast cancer cells than in normal breast epithelial cells. In MCF-7 cells, miR-6838-5p overexpression induced significant inhibition of cell proliferation. Dual luciferase reporter gene experiment demonstrated a binding relationship between miR-6838-5p and DDR1 (P<0.01). Western blotting showed that miR-6838-5p overexpression significantly lowered DDR1 expression in MCF-7 cells, and DDR1 overexpression promoted proliferation of the cells; co-transfection of the cells with DDR1-overexpressing vector significantly attenuated the inhibitory effect of miR-6838-5p mimic on cell proliferation. In the tumor-bearing nude mice, the xenografts overexpressing miR-6838-5p showed a significantly smaller volum with obviously the expression of DDR1. Conclusion Overexpression of miR-6838-5p inhibits breast cancer cell proliferation by regulating DDR1 expression.

Key words: miR-6838-5p, brest cancer, DDR1, cell proliferation