Basic & Clinical Medicine ›› 2025, Vol. 45 ›› Issue (12): 1580-1587.doi: 10.16352/j.issn.1001-6325.2025.12.1580

• Original Articles • Previous Articles     Next Articles

miR-141-3p down-regulating lysophosphatidic acid receptor3 inhibits proliferation, migration and epithelial-mesenchymal transition of brain glioma cells

LI Wenhui1, REN Honggang1, GUO Jian1, SONG Yang1, FENG Fuqiang2*   

  1. 1. Department of Neurosurgery, Linfen People′s Hospital, Linfen 041000;
    2. Department of Neurosurgery, Shanxi Cancer Hospital, Chinese Academy of Medical Sciences Cancer Hospital Shanxi Hospital, the Affiliated Cancer Hospital of Shanxi Medical University, Taiyuan 030013, China
  • Received:2025-01-16 Revised:2025-03-25 Online:2025-12-05 Published:2025-11-25
  • Contact: *doctorfengfuqiang@163.com

Abstract: Objective To investigate the impacts of miR-141-3p on the proliferation, migration and epithelial-mesenchymal transformation of glioma cells by regulating lysophosphatidic acid receptor 3 (LPAR3). Methods RT-qPCR was used to detect the level of miR-141-3p and LPAR3 in glioma tissues and cells. Dual luciferase was used to detect the targeting relationship between miR-141-3p and LPAR3. The cells were divided into control group, miR-NC group, miR-141-3p mimics group, miR-141-3p mimics+pcDNA3.1 group, and miR-141-3p mimics+pcDNA-LPAR3 group, and then transfected with corresponding plasmids. RT-qPCR was used to detect the level of miR-141-3p and LPAR3 in cells. EdU method was used to detect cell proliferation. The scratch healing experiment was used to detect cell migration. Western blot was used to detect the expression of proteins related to cell proliferation, migration, and epithelial-mesenchymal transformation. Xenograft tumor model in nude mice was used to observe tumor formation. RT-qPCR was used to detect the level of miR-141-3p in tumor tissue. In addition, Western blot was performed to detect the expression of LPAR3, PCNA, and MMP-2. Results miR-141-3p was downregulated, whereas LPAR3 mRNA was upregulated in glioma tissues and U251, T98G, and CHG-5 cell lines (P<0.05). There was a targeted binding site between miR-141-3p and LPAR3. miR-141-3p mimics significantly increased the expression of miR-141-3p and E-cadherin, but decreased LPAR3 mRNA level, EdU-positive rate, scratch wound healing rate, and the expression of PCNA, cyclin D1, MMP-2, MMP-9, N-cadherin, and vimentin (P<0.05). pcDNA-LPAR3 reversed effect on expression of these factors (P<0.05). Tumor transplantation experiments in nude mice showed that miR-141-3p mimics reduced tumor volume, tumor weight, LPAR3, PCNA, and MMP-2 expression, and increased the level of miR-141-3p (P<0.05). Conclusions miR-141-3p can inhibit proliferation, migration, and epithelial-mesenchymal transformation of glioma cells by down-regulating LPAR3.

Key words: miR-141-3p, lysophosphatidic acid receptor 3, glioma cell, proliferation, epithelial-mesenchymal transformation

CLC Number: