Department of Gynecology, Hubei Provincial Maternal and Child Health Hospital, Tongji Medical College, Huazhong University of Science and Technology, No.745 Wuluo Road, Hongshan District, Wuhan City, Hubei Province, 430070, People's Republic of China.
Mol Cell Biochem. 2022 May;477(5):1463-1475. doi: 10.1007/s11010-022-04371-x. Epub 2022 Feb 15.
Recent studies have shown that prostate cancer-associated long non-coding RNA, PRNCR1, plays crucial roles in the development of multiple human cancers. However, its role in ovarian cancer is barely known. This study was carried out to investigate the role of PRNCR1 and the underlying mechanisms in OC. The expression of PRNCR1 and miR-653-5p in OC cell lines and tissues were detected by qRT-PCR. The expression of ELF2 protein was evaluated by Western blot analysis. Cell proliferation was measured by colony formation and MTT assay. Cell invasion and migration were evaluated by Transwell and wound healing assay. Luciferase reporter assay and RNA-binding protein immunoprecipitation assay were performed to determine the interaction between miR-653-5p and PRNCR1, as well as between miR-653-5p and ELF2. In vivo tumor xenograft model was established to evaluate the role of PRNCR1 in tumor growth. Our results demonstrated that PRNCR1 was significantly upregulated in both OC cell lines and tissues, and high expression of PRNCR1 was correlated with poor survival of OC patients. Overexpression of PRNCR1 accelerated OC cell invasion, migration and proliferation. Besides, the expression of PRNCR1 was negatively correlated with the expression of miR-653-5p, while positively correlated with the expression of E74-like factor 2 in OC tissues. Importantly, ELF2 could target miR-653-5p, and PRNCR1 increased the expression levels of ELF2 by sponging miR-653-5p in OC cells. Furthermore, the miR-145-5p/ELF2 axis was involved in the regulation of PRNCR1 in OC progression in vivo. PRNCR1 promotes OC tumor progress via the miR-653-5p/ELF2 axis and might be a potential therapeutic target for OC.
最近的研究表明,前列腺癌相关的长非编码 RNA(PRNCR1)在多种人类癌症的发展中发挥着关键作用。然而,其在卵巢癌中的作用鲜为人知。本研究旨在探讨 PRNCR1 在 OC 中的作用及其潜在机制。通过 qRT-PCR 检测 OC 细胞系和组织中 PRNCR1 和 miR-653-5p 的表达。通过 Western blot 分析评估 ELF2 蛋白的表达。通过集落形成和 MTT 测定法测量细胞增殖。通过 Transwell 和划痕愈合测定法评估细胞侵袭和迁移。通过荧光素酶报告基因检测和 RNA 结合蛋白免疫沉淀测定法来确定 miR-653-5p 与 PRNCR1 之间以及 miR-653-5p 与 ELF2 之间的相互作用。建立体内肿瘤异种移植模型以评估 PRNCR1 在肿瘤生长中的作用。我们的结果表明,PRNCR1 在 OC 细胞系和组织中均显著上调,PRNCR1 的高表达与 OC 患者的不良生存相关。过表达 PRNCR1 可加速 OC 细胞侵袭、迁移和增殖。此外,PRNCR1 的表达与 OC 组织中 miR-653-5p 的表达呈负相关,与 E74 样因子 2 的表达呈正相关。重要的是,ELF2 可以靶向 miR-653-5p,而 PRNCR1 通过在 OC 细胞中海绵吸附 miR-653-5p 来增加 ELF2 的表达水平。此外,miR-145-5p/ELF2 轴参与了 PRNCR1 在 OC 体内进展中的调节。PRNCR1 通过 miR-653-5p/ELF2 轴促进 OC 肿瘤进展,可能成为 OC 的潜在治疗靶点。