Volume 20 Issue 5
May  2022
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GU Shao-jun, QIAN Chun-yan, FU Huan-quan. Experimental study of miR-613 targeting PTBP1 to inhibit the invasion and migration of endometrial cancer cells[J]. Chinese Journal of General Practice, 2022, 20(5): 781-784. doi: 10.16766/j.cnki.issn.1674-4152.002453
Citation: GU Shao-jun, QIAN Chun-yan, FU Huan-quan. Experimental study of miR-613 targeting PTBP1 to inhibit the invasion and migration of endometrial cancer cells[J]. Chinese Journal of General Practice, 2022, 20(5): 781-784. doi: 10.16766/j.cnki.issn.1674-4152.002453

Experimental study of miR-613 targeting PTBP1 to inhibit the invasion and migration of endometrial cancer cells

doi: 10.16766/j.cnki.issn.1674-4152.002453
Funds:

 LGF19H200002

  • Received Date: 2021-11-21
    Available Online: 2022-09-05
  •   Objective  To investigate the effects of miR-613 targeting polypyrimidine tract-binding protein 1 (PTBP1) on the proliferation, migration and invasion of endometrial cancer cells (Ishikawa).  Methods  Real-time fluorescent quantitative PCR (RT-qPCR) was conducted to detect the expression of miR-613 and PTBP1 mRNA in endometrial cancer tissues. Ishikawa cells were cultured in vitro, and intervened to overexpress miR-613, inhibit PTBP1 expression, or co-overexpress miR-613 and PTBP1. The proliferation, migration and invasion of Ishikawa cells and the protein expression levels of PTBP1, matrix metalloproteinase-2(MMP-2) and MMP-9 were detected respectively. Dual-luciferase reporter assay was conducted to verify the targeting relationship between miR-613 and PTBP1.  Results  The expression level of miR-613 in endometrial cancer tissue was 0.48±0.09, which was significantly lower than that in paracancerous tissue (1.03±0.11, P < 0.05). The expression level of PTBP1 mRNA was 2.78±0.23, which was significantly higher than that in paracancerous tissue (1.01±0.12, P < 0.05). MiR-613 was negatively correlated with PTBP1 mRNA (r=-0.523, P < 0.05). The results of dual-luciferase reporter gene assay showed that miR-613 targeted and negatively regulated the expression of PTBP1. Overexpression of miR-613 and inhibition of PTBP1 expression significantly decreased the survival rate of Ishikawa cells, the number of cell migration and invasion, and the expression levels of PTBP1, MMP-2 and MMP-9 (all P < 0.05). Overexpression of PTBP1 reversed the inhibitory effects of overexpression of miR-613 on Ishikawa cell proliferation, migration and invasion.  Conclusion  The expression of miR-613 is low in endometrial cancer tissues. Overexpression of miR-613 can inhibit the proliferation, migration and invasion of human endometrial cancer cells by targeting and inhibiting the expression of PTBP1.

     

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  • [1]
    PASSARELLO K, KURIAN S, VILLANUEVA V. Endometrial cancer: An overview of pathophysiology, management, and care[J]. Semin Oncol Nurs, 2019, 35(2): 157-165. doi: 10.1016/j.soncn.2019.02.002
    [2]
    梁磊, 杨波, 吴园园, 等. MiR-556-3p通过靶基因SASH1调控子宫内膜癌细胞的活力、迁移和侵袭[J]. 中国病理生理杂志, 2020, 36(12): 2174-2181. doi: 10.3969/j.issn.1000-4718.2020.12.008

    LIANG L, YANG B, WU Y Y, et al. miR-556-3p regulates viability, migration and invasion of endometrial cancer cells by targeting SASH1[J]. Chinese Journal of Pathophysiology, 2020, 36(12): 2174-2181. doi: 10.3969/j.issn.1000-4718.2020.12.008
    [3]
    WANG J, YANG S, GE W, et al. MiR-613 suppressed the laryngeal squamous cell carcinoma progression through regulating PDK1[J]. J Cell Biochem, 2018, 119(7): 5118-5125. doi: 10.1002/jcb.26468
    [4]
    YAN Z, YIN H, LIN G. CircDDX42 Accelerates the development of pancreatic cancer via miR-613/ID4/PI3K/AKT axis[J]. Onco Targets Ther, 2020, 13(1): 10945-10957.
    [5]
    周春, 王光华, 张帮柱, 等. miR-613对高尔基体磷蛋白3调控乳腺癌细胞增殖, 迁移和侵袭的研究[J]. 中国临床药理学杂志, 2020, 36(19): 3066-3069. https://www.cnki.com.cn/Article/CJFDTOTAL-GLYZ202019028.htm

    ZHOU C, WANG G H, ZHANG B Z, et al. Mechanism of miR-613 targeting golgi phosphoprotein 3 regulating the proliferation, migration and invasion of breast cancer cells[J]. Chinese J Clin Pharmacol, 2020, 36(19): 3066-3069. https://www.cnki.com.cn/Article/CJFDTOTAL-GLYZ202019028.htm
    [6]
    TANIGUCHI K, UCHIYAMA K, AKAO Y. PTBP1-targeting microRNAs regulate cancer-specific energy metabolism through the modulation of PKM1/M2 splicing[J]. Cancer Sci, 2021, 112(1): 41-50. doi: 10.1111/cas.14694
    [7]
    李雅睿, 任牡丹, 卢桂芳, 等. 多聚嘧啶区结合蛋白1对胃癌细胞增殖和转移的作用机制[J]. 中华消化杂志, 2021, 41(2): 100-106. doi: 10.3760/cma.j.cn311367-20200723-00454

    LI Y R, REN M D, LU G F, et al. Mechanism of polypyrimidine tract-binding protein 1 on the proliferation and metastasis of gastric cancer cells[J]. Chin J Dig, 2021, 41(2): 100-106. doi: 10.3760/cma.j.cn311367-20200723-00454
    [8]
    王攀, 王毅超, 虞丹丹, 等. miR-1246在肝癌血清中的表达及对肝癌HepG2细胞生物学功能的影响[J]. 中华全科医学, 2021, 19(8): 1292-1295. doi: 10.16766/j.cnki.issn.1674-4152.002043

    WANG P, WANG Y C, YU D D, et al. Expression of microRNA-1246 in the serum of hepatocellular carcinoma and its effect on biological function of HepG2 cells[J]. Chinese general practice, 2021, 19(8): 1292-1295. doi: 10.16766/j.cnki.issn.1674-4152.002043
    [9]
    LIANG J, XU H, DU Y N, et al. Exosomal miR-499a-5p inhibits endometrial cancer growth and metastasis via targeting VAV3[J]. Cancer Manag Res, 2020, 12(1): 13541-13552.
    [10]
    LIU C, JIANG Y, HAN B. miR-613 Suppresses Chemoresistance and stemness in triple-negative breast cancer by targeting FAM83A[J]. Cancer Manag Res, 2020, 12(1): 12623-12633.
    [11]
    曾保征, 王赣, 陈超, 等. miR-613在肝细胞癌中的表达变化及其对癌细胞增殖, 凋亡及侵袭, 迁移能力的影响[J]. 山东医药, 2020, 60(10): 41-44. doi: 10.3969/j.issn.1002-266X.2020.10.010

    ZENG B Z, WANG G, CHEN C, et al. Expression of miR-613 in hepatocellular carcinoma and its effects on proliferation, apoptosis, invasion and migration of cancer cells[J]. Shandong Med J, 2020, 60(10): 41-44. doi: 10.3969/j.issn.1002-266X.2020.10.010
    [12]
    REN W, LI C, DUAN W, et al. MicroRNA-613 represses prostate cancer cell proliferation and invasion through targeting Frizzled7[J]. Biochem Biophys Res Commun, 2016, 469(3): 633-638. doi: 10.1016/j.bbrc.2015.12.054
    [13]
    JI H, HU N J. MiR-613 blocked the progression of cervical cancer by targeting LETM1[J]. Eur Rev Med Pharmacol Sci, 2020, 24(12): 6576-6582.
    [14]
    ZHU W, ZHOU B L, RONG L J, et al. Roles of PTBP1 in alternative splicing, glycolysis, and oncogensis[J]. J Zhejiang Univ Sci B, 2020, 21(2): 122-136. doi: 10.1631/jzus.B1900422
    [15]
    KANG H, HEO S, SHIN J J, et al. A miR-194/PTBP1/CCND3 axis regulates tumor growth in human hepatocellular carcinoma[J]. J Pathol, 2019, 249(3): 395-408. doi: 10.1002/path.5325
    [16]
    沈良华, 吴璐华, 张仙丽, 等. PTBP1通过EMT途径促进肝癌细胞的迁移与侵袭[J]. 中国病理生理杂志, 2019, 35(10): 1819-1825. https://www.cnki.com.cn/Article/CJFDTOTAL-ZBLS201910013.htm

    SHEN L H, WU L H, ZHANG X L, et al. PTBP1 promotes migration and invasion of liver cancer cells through EMT pathway[J]. Chinese Journal of Pathophysiology, 2019, 35(10): 1819-1825. https://www.cnki.com.cn/Article/CJFDTOTAL-ZBLS201910013.htm
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