Chinese Journal of Clinical Anatomy ›› 2019, Vol. 37 ›› Issue (3): 292-298.doi: 10.13418/j.issn.1001-165x.2019.03.011

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The regulatory effects of miR-143-3p on proliferation, apoptosis and invasion on human colon cancer cell via targeting MAPK1

ZHANG Zhi-qian1, ZHANG Guang-xin2, PENG Xiao-dong2   

  1. 1. Department of General Surgery, The Third Hospital of Nanchang,Nanchang 330009, China; 2. Department of Medicine Oncology, The First Affiliated Hospital of Nanchang University, Nanchang 330006, China
  • Received:2018-09-26 Online:2019-05-25 Published:2019-06-13

Abstract: Objective To investigate the relationship between miR-143-3p targeting MAPK1 and its effect on proliferation, apoptosis and invasion of human colon cancer cells. Methods qRT-PCR was used to detect the effect of transfection and the expression level of MAPK1 mRNA. Double luciferase reporter assay was used to detect the targeting relationship between microRNAs-143-3p and MAPK1. The expression level of MAPK1 protein was detected by Western blot. The proliferation multiple was detected by CCK-8. The proliferation was detected by Hoechst staining. The cell invasion was detected by in vitro invasion test. The expression of Ki67, VEGF,MMP-2 and claspase-3 was detected by Western blot. Results miR-143-3p mimic inhibited the expression of MAPK1 mRNA and protein in SW620 cells. miR-143-3p mimic and MAPK1 wild-type reporter plasmid decreased the activity of luciferase significantly. After miR-143-3p mimic transfection, the proliferation and invasion of SW620 cells were significantly decreased, the number of apoptotic cells was significantly increased, the expression of Ki67, VEGF and MMP-2 was significantly decreased, and the expression of cl-caspase-3 was significantly increased. The miR-143-3p mimic alleviated the induction effect of high expression of MAPK1 on proliferation and invasion of SW620 cells and inhibition effect on cell apoptosis. Conclusion miR-143-3p can inhibit proliferation and invasion of human colon cancer cells and induce apoptosis through possible targeting inhibition of MAPK1.

Key words: Colon cancer,  Micro RNA,  MAPK1,  Proliferation,  Apoptosis,  Invasion

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