Department of Gynaecology, Changzhou No.2 People's Hospital, Changzhou, Jiangsu 213000, China.
Acta Biochim Pol. 2021 Jun 28;68(4):673-677. doi: 10.18388/abp.2020_5546.
The specific objective of this investigation is to explore the impact of miR-198 on proliferation, migration as well as invasion of ovarian cancer (OC) cells.
OC tissue and adjacent normal tissue samples from OC patients were collected, and normal human ovarian epithelial cell IOSE80 and OC cell lines SKOV3, Caov3, A2780 and OVCAR3 were selected in this study for investigation. MiR-198 expression level was assessed using RT-qPCR. MTT, colony formation assay, Transwell and wound healing assay, and flow cytometry were adopted to analyze the role of miR-198 in OVCAR cell proliferation, invasion, migration, as well as apoptosis. Meanwhile, the levels of P13K/Akt signaling pathway-related proteins were determined by western blotting.
A significant decrease in miR-198 level was revealed in the OC tissues and cells, contributing to the promotion of OVCAR3 cells in terms of proliferation, migration, invasion, and inhibition of apoptosis. MiR-198 overexpression had an opposite effect on these biological processes of OVCAR3 cells. Further study found that down-regulation of miR-198 caused a significant increase in the activity of PI3K/Akt signaling pathway in the OVCAR3 cells. In contrast, overexpressed miR-198 led to inhibition of this pathway's activity.
MiR-198 may possess an ability to inhibit activation of the P13K/Akt pathway, thus suppressing the OC cell proliferation, migration, as well as invasion.
本研究的具体目的是探讨 miR-198 对卵巢癌细胞(OC)增殖、迁移和侵袭的影响。
收集 OC 患者的 OC 组织和相邻正常组织样本,并选择正常人类卵巢上皮细胞 IOSE80 和 OC 细胞系 SKOV3、Caov3、A2780 和 OVCAR3 进行研究。采用 RT-qPCR 评估 miR-198 表达水平。采用 MTT、集落形成实验、Transwell 和划痕愈合实验以及流式细胞术分析 miR-198 在 OVCAR 细胞增殖、侵袭、迁移和凋亡中的作用。同时,采用 Western blot 测定 P13K/Akt 信号通路相关蛋白水平。
OC 组织和细胞中 miR-198 水平显著降低,促进了 OVCAR3 细胞的增殖、迁移、侵袭和抑制凋亡。miR-198 的过表达对 OVCAR3 细胞的这些生物学过程产生了相反的影响。进一步的研究发现,下调 miR-198 导致 OVCAR3 细胞中 PI3K/Akt 信号通路的活性显著增加。相反,过表达 miR-198 导致该通路的活性受到抑制。
miR-198 可能具有抑制 P13K/Akt 通路激活的能力,从而抑制 OC 细胞的增殖、迁移和侵袭。