Department of Urology, Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University, Jinan, Shandong 250021, China.
Department of Urology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong 250021, China.
Aging (Albany NY). 2021 Apr 13;13(8):12113-12128. doi: 10.18632/aging.202919.
Long non-coding RNAs are key regulators of tumor development and progression, with the potential to be biomarkers of tumors. This study aimed to explore the role of PlncRNA-1 in the progression of prostate cancer (PCa). We found that PlncRNA-1 was up-regulated in 85.29% of PCa tissues and could predict the T stage of PCa patients to a certain extent. Results showed that inhibition of PlncRNA-1 expression potentially promoted cell apoptosis, suppressed the proliferation, migration, and invasion of cells, and triggered G2/M cycle arrest and . PlncRNA-1 was mainly localized in the nucleus and PlncRNA-1 expression and phosphatase and tensin homologue (PTEN) expression were negatively correlated. Mechanistically, knockdown of PlncRNA-1 increased expression levels of PTEN protein and phosphorylated PTEN protein, and decreased expression levels of Akt protein and phosphorylated Akt protein. Rescue experiments demonstrated that PTEN inhibitors abolished the changes in PTEN/Akt pathway caused by PlncRNA-1 interference. PlncRNA-1 can promote the occurrence and development of PCa via the PTEN/Akt pathway. PlncRNA-1 may, therefore, be a new candidate target for the treatment of PCa.
长非编码 RNA 是肿瘤发生和发展的关键调节因子,具有成为肿瘤标志物的潜力。本研究旨在探讨 PlncRNA-1 在前列腺癌 (PCa) 进展中的作用。我们发现 PlncRNA-1 在 85.29%的 PCa 组织中上调,并在一定程度上可以预测 PCa 患者的 T 分期。结果表明,抑制 PlncRNA-1 的表达可能促进细胞凋亡,抑制细胞的增殖、迁移和侵袭,并引发 G2/M 周期阻滞。PlncRNA-1 主要定位于细胞核,PlncRNA-1 的表达与磷酸酶和张力蛋白同源物 (PTEN) 的表达呈负相关。在机制上,敲低 PlncRNA-1 增加了 PTEN 蛋白和磷酸化 PTEN 蛋白的表达水平,降低了 Akt 蛋白和磷酸化 Akt 蛋白的表达水平。挽救实验表明,PTEN 抑制剂消除了 PlncRNA-1 干扰引起的 PTEN/Akt 通路的变化。PlncRNA-1 可以通过 PTEN/Akt 通路促进 PCa 的发生和发展。因此,PlncRNA-1 可能成为治疗 PCa 的新候选靶点。