Fredes-Garrido Allison, Cruz Álvaro Armijo, Calaf Gloria M, Garrido Maritza P, Romero Carmen
Laboratory of Endocrinology and Reproductive Biology, Clinical Hospital University of Chile, Santiago 8380456, Chile.
Institute of Advanced Research, University of Tarapacá, Arica 1000000, Chile.
Mol Med Rep. 2025 Sep;32(3). doi: 10.3892/mmr.2025.13611. Epub 2025 Jul 11.
MicroRNAs (miRs) are non‑coding RNAs that prevent the translation of mRNAs. miRs participate in cellular processes such as cell proliferation, migration and invasion, acting as oncogenes or tumor suppressors. In epithelial ovarian cancer (EOC), a decrease in tumor suppressor miRs, such as miR‑145 and miR‑23b, regulates the mRNAs of oncogenic proteins. The present study aimed to determine whether the co‑transfection of two oncosuppressor miRs (miR‑145‑5p and miR‑23b‑3p) decreased the proliferation, migration, invasion, and protein levels of c‑MYC, zinc finger E‑box binding homeobox 1 (ZEB1) and ATP binding cassette subfamily B1 (ABCB1) in EOC cell lines (A2780, SKOV‑3 and OV‑90). Reverse transcription‑quantitative PCR was employed to determine miR expression after co‑transfection. Cell proliferation was evaluated by Ki‑67 immunofluorescence staining and Ki‑67 positive cell counting. Transwell inserts, both with and without Matrigel, were used to assess invasion and migration, respectively. c‑MYC, ZEB1 and ABCB1 protein expression was determined by western blot analysis. The co‑transfection of miR‑145 and miR‑23b resulted in decreased proliferation, migration and invasion, along with reduced protein expression levels of c‑MYC, ZEB1 and ABCB1 in EOC cells. The combination of miR‑23b and miR‑145 transfection in EOC cells exhibited good antitumor effects, thus supporting the design of future complementary therapies for EOC.
微小RNA(miR)是一类非编码RNA,可阻止信使核糖核酸(mRNA)的翻译。miR参与细胞增殖、迁移和侵袭等细胞过程,可作为癌基因或肿瘤抑制因子发挥作用。在上皮性卵巢癌(EOC)中,肿瘤抑制性miR(如miR-145和miR-23b)的减少会调节致癌蛋白的mRNA。本研究旨在确定两种抑癌miR(miR-145-5p和miR-23b-3p)共转染是否会降低EOC细胞系(A2780、SKOV-3和OV-90)中c-MYC、锌指E盒结合同源框1(ZEB1)和ATP结合盒亚家族B1(ABCB1)的增殖、迁移、侵袭及蛋白水平。采用逆转录定量聚合酶链反应(RT-qPCR)来测定共转染后miR的表达。通过Ki-67免疫荧光染色和Ki-67阳性细胞计数评估细胞增殖。分别使用带有和不带有基质胶的Transwell小室评估侵袭和迁移。通过蛋白质印迹分析确定c-MYC、ZEB1和ABCB1蛋白表达。miR-145和miR-23b共转染导致EOC细胞的增殖、迁移和侵袭减少,同时c-MYC、ZEB1和ABCB1的蛋白表达水平降低。在EOC细胞中共转染miR-23b和miR-145表现出良好的抗肿瘤作用,从而为未来EOC的辅助治疗设计提供了支持。