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miR-197-3p通过靶向卵巢癌细胞中的ABCA7减少上皮-间质转化。

miR-197-3p reduces epithelial-mesenchymal transition by targeting ABCA7 in ovarian cancer cells.

作者信息

Xie Weiquan, Shui Chengyu, Fang Xiping, Peng Yuqiu, Qin Li

机构信息

Department of Obstetrics and Gynaecology, The Central Hospital of Enshi Tujia and Miao Autonomous Prefecture, Enshi, 445000 Hubei China.

Department of Oncology, The Central Hospital of Enshi Tujia and Miao Autonomous Prefecture, No. 158 Wuyang Avenue, Enshi, 445000 Hubei China.

出版信息

3 Biotech. 2020 Aug;10(8):375. doi: 10.1007/s13205-020-02362-7. Epub 2020 Aug 4.

Abstract

The present study was designed to explore the role of microRNA-197-3p in regulating the epithelial-mesenchymal cellular transition in ovarian cancer. The results showed that miR-197 to be significantly ( < 0.05) downregulated in human ovarian cancer tissues and cell lines. Overexpression of miR-197 significantly ( < 0.05) reduced the proliferation of OVACAR-3 cancer cells. Additionally, the colony formation of the OVACAR-3 cells was inhibited by 59% relative to control. The migration and invasion of the OVACAR-3 cells was inhibited by 64% and 72%, respectively, upon miR-197 overexpression. Western blot analysis showed miR-197 was found to upregulate the expression of E-cadherin, while the expression of N-cadherin, vimentin, and snail proteins was found to decrease significantly ( < 0.05). TargetScan analysis together with dual luciferase assay revealed that miR-197 exerts its effects by targeting ABCA7 in ovarian cancer. ABCA7 was significantly ( < 0.05) overexpressed in ovarian cancer tissues and cell lines. However, silencing of ABCA7 resulted in significant inhibition of cell proliferation, migration, and invasion. Nonetheless, overexpression of ABCA7 could abolish the tumor-suppressive effects of miR-197 on the OVACAR-3 cells. Taken together, miR-197 acts a tumor-suppressive in ovarian cancer and points towards its therapeutic implications in the treatment of ovarian cancer.

摘要

本研究旨在探讨微小RNA-197-3p在调控卵巢癌上皮-间质细胞转化中的作用。结果显示,miR-197在人卵巢癌组织和细胞系中显著下调(<0.05)。miR-197的过表达显著(<0.05)降低了OVACAR-3癌细胞的增殖。此外,相对于对照组,OVACAR-3细胞的集落形成受到59%的抑制。miR-197过表达后,OVACAR-3细胞的迁移和侵袭分别受到64%和72%的抑制。蛋白质印迹分析显示,miR-197可上调E-钙黏蛋白的表达,而N-钙黏蛋白、波形蛋白和蜗牛蛋白的表达则显著降低(<0.05)。TargetScan分析和双荧光素酶测定共同表明,miR-197在卵巢癌中通过靶向ABCA7发挥作用。ABCA7在卵巢癌组织和细胞系中显著过表达(<0.05)。然而,ABCA7的沉默导致细胞增殖、迁移和侵袭受到显著抑制。尽管如此,ABCA7的过表达可消除miR-197对OVACAR-3细胞的肿瘤抑制作用。综上所述,miR-197在卵巢癌中发挥肿瘤抑制作用,并指出其在卵巢癌治疗中的潜在治疗意义。

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