Department of Medical Oncology, Lishui Municipal Central Hospital, Lishui 323000, Zhejiang, China.
Curr Pharm Des. 2021;27(46):4663-4670. doi: 10.2174/1381612827666210827104828.
Long non-coding RNAs (lncRNAs) have been reported to play important roles in cellular biological function. Aberrant expression of lncRNAs has been found to be related to the progression of various diseases. LncRNA prostate cancer gene expression marker 1 (PCGEM1) has been demonstrated to be involved in the initiation and progression of human cancers. However, to date, the clinical and functional significance of PCGEM1 expression in NSCLC progression remains unknown.
The expression of LncRNA PCGEM1 and miR-152-3p in NSCLC tissues and cells was analyzed using quantitative real-time RT-PCR. Experiments using NSCLC cells were conducted to explore the influence of PCGEM1 on tumor cell proliferation, migration and invasion.
Increased expression of PCGEM1 was observed in NSCLC tissues and cells compared with the corresponding controls (all P < 0.001). PCGEM1 expression was associated with NSCLC patients' lymph node metastasis and TNM stage (all P < 0.05), and the knockdown of PCGEM1 in NSCLC cells led to inhibited cell proliferation, migration and invasion. The further luciferase reporter assay and expression results showed that miR-152-3p might be a target gene of PCGEM1 and mediate the effects of PCGEM1 on cell proliferation, migration and invasion in NSCLC.
Thus, the findings from the present study indicate that the NSCLC patients have significantly increased PCGEM1 and decreased miR-152-3p expression and that the knockdown of PCGEM1 may inhibit NSCLC cell proliferation, migration and invasion by sponging miR-152-3p. The PCGEM1/miR-152-3p axis may provide novel therapeutic targets for NSCLC treatment.
长链非编码 RNA(lncRNA)在细胞生物学功能中发挥着重要作用。lncRNA 的异常表达与各种疾病的进展有关。已经证明 lncRNA 前列腺癌基因表达标记 1(PCGEM1)参与了人类癌症的发生和发展。然而,迄今为止,PCGEM1 在非小细胞肺癌(NSCLC)进展中的临床和功能意义仍不清楚。
使用实时定量 RT-PCR 分析 NSCLC 组织和细胞中 LncRNA PCGEM1 和 miR-152-3p 的表达。使用 NSCLC 细胞进行实验,以探讨 PCGEM1 对肿瘤细胞增殖、迁移和侵袭的影响。
与相应对照相比,NSCLC 组织和细胞中观察到 PCGEM1 的表达增加(均 P < 0.001)。PCGEM1 表达与 NSCLC 患者的淋巴结转移和 TNM 分期有关(均 P < 0.05),并且在 NSCLC 细胞中敲低 PCGEM1 导致细胞增殖、迁移和侵袭受到抑制。进一步的荧光素酶报告基因检测和表达结果表明,miR-152-3p 可能是 PCGEM1 的靶基因,并介导 PCGEM1 对 NSCLC 细胞增殖、迁移和侵袭的影响。
因此,本研究表明 NSCLC 患者的 PCGEM1 表达显著增加,miR-152-3p 表达降低,敲低 PCGEM1 可能通过海绵吸附 miR-152-3p 抑制 NSCLC 细胞增殖、迁移和侵袭。PCGEM1/miR-152-3p 轴可能为 NSCLC 的治疗提供新的治疗靶点。