Department of Gynaecology and Obstetrics, People's Hospital of Lishui City, The Sixth Affiliated Hospital of Wenzhou Medical University, The Affiliated Hospital of Lishui College, Lishui, Zhejiang 323000, P.R. China.
Mol Med Rep. 2021 May;23(5). doi: 10.3892/mmr.2021.12026. Epub 2021 Mar 24.
Circular RNA ABCB10 (circ‑ABCB10) modulates cellular functions and microRNA (miR)‑1271 in epithelial ovarian cancer (EOC). The present study aimed to investigate the interaction between circ‑ABCB10 and miR‑1271 in regulating EOC cellular function and the calpain small subunit 1 (Capn4)/Wnt/β‑catenin signaling pathway. circ‑ABCB10 and miR‑1271 expression levels were detected in EOC cells (OVCAR3, UWB1.289, SKOV3 and CAOV3) and normal ovarian epithelial cells (IOSE80) via reverse‑transcription quantitative PCR. SKOV3 cells were transfected with control short hairpin (sh)RNA plasmids, control inhibitor, circ‑ABCB10 shRNA plasmids and miR‑1271 inhibitor. UWB1.289 cells were transfected with control overexpression plasmids, control mimic, circ‑ABCB10 overexpression plasmids and miR‑1271 mimic. Subsequently, cell proliferation, apoptosis, invasion and the Capn4/Wnt/β‑catenin signaling pathway were assessed. In addition, a luciferase activity assay was performed. circ‑ABCB10 expression was significantly increased in OVCAR3, SKOV3 and CAOV3 cells compared with IOSE80 cells, but was not significantly altered in UWB1.289 cells. miR‑1271 expression was significantly decreased in OVCAR3, UWB1.289, SKOV3 and CAOV3 cells compared with IOSE80 cells. In both SKOV3 and UWB1.289 cells, circ‑ABCB10 negatively regulated miR‑1271, whereas miR‑1271 did not affect circ‑ABCB10. Furthermore, circ‑ABCB10 enhanced cell proliferation, invasion and the Capn4/Wnt/β‑catenin signaling pathway, but inhibited cell apoptosis, whereas miR‑1271 suppressed cell proliferation, invasion and the Capn4/Wnt/β‑catenin signaling pathway, but facilitated cell apoptosis. Moreover, miR‑1271 attenuated the proproliferative, proinvasive and antiapoptotic effects of circ‑ABCB10, and reversed the positive regulation of circ‑ABCB10 on the Capn4/Wnt/β‑catenin signaling pathway. Besides, the luciferase activity assay indicated that circ‑ABCB10 directly bound to miR‑1271. In conclusion, the present study indicated that circ‑ABCB10 promoted cell proliferation and invasion, and suppressed apoptosis by regulating the miR‑1271‑mediated Capn4/Wnt/β‑catenin signaling pathway in EOC.
环状 RNA ABCB10(circ-ABCB10)调节上皮性卵巢癌(EOC)中的细胞功能和微小 RNA(miR)-1271。本研究旨在探讨 circ-ABCB10 与 miR-1271 之间的相互作用,以调节 EOC 细胞功能和钙蛋白酶小亚基 1(Capn4)/Wnt/β-连环蛋白信号通路。通过逆转录定量 PCR 检测 EOC 细胞(OVCAR3、UWB1.289、SKOV3 和 CAOV3)和正常卵巢上皮细胞(IOSE80)中 circ-ABCB10 和 miR-1271 的表达水平。用对照短发夹(sh)RNA 质粒、对照抑制剂、circ-ABCB10 shRNA 质粒和 miR-1271 抑制剂转染 SKOV3 细胞。用对照过表达质粒、对照模拟物、circ-ABCB10 过表达质粒和 miR-1271 模拟物转染 UWB1.289 细胞。随后,评估细胞增殖、凋亡、侵袭和 Capn4/Wnt/β-连环蛋白信号通路。此外,还进行了荧光素酶活性测定。与 IOSE80 细胞相比,OVCAR3、SKOV3 和 CAOV3 细胞中 circ-ABCB10 的表达显著增加,但 UWB1.289 细胞中的表达无显著变化。与 IOSE80 细胞相比,OVCAR3、UWB1.289、SKOV3 和 CAOV3 细胞中 miR-1271 的表达显著降低。在 SKOV3 和 UWB1.289 细胞中,circ-ABCB10 负调控 miR-1271,而 miR-1271 不影响 circ-ABCB10。此外,circ-ABCB10 增强细胞增殖、侵袭和 Capn4/Wnt/β-连环蛋白信号通路,但抑制细胞凋亡,而 miR-1271 抑制细胞增殖、侵袭和 Capn4/Wnt/β-连环蛋白信号通路,但促进细胞凋亡。此外,miR-1271 减弱了 circ-ABCB10 的促增殖、促侵袭和抗凋亡作用,并逆转了 circ-ABCB10 对 Capn4/Wnt/β-连环蛋白信号通路的正向调节。此外,荧光素酶活性测定表明 circ-ABCB10 可直接与 miR-1271 结合。综上所述,本研究表明,circ-ABCB10 通过调节 miR-1271 介导的 Capn4/Wnt/β-连环蛋白信号通路,在上皮性卵巢癌中促进细胞增殖和侵袭,抑制细胞凋亡。