Department of Oncology, Changle People's Hospital, Weifang, China.
Department of Thoracic Surgery, Yidu Central Hospital of Weifang, Weifang, China.
Cell Cycle. 2023 Apr;22(7):808-817. doi: 10.1080/15384101.2022.2154556. Epub 2022 Dec 18.
As a type of lung cancer, non-small cell lung cancer (NSCLC) has the characteristics of high mortality and high recurrence rate, which poses a great threat to human life and health. Due to the high risk of surgical treatment and the slow recovery of wounds, non-coding RNAs, especially lncRNAs are used as new potential clinical prognostic markers to prevent and treat cancer in advance. This study aims to explore the role of FAM138B in NSCLC and its possibility as a prognostic biomarker. Real-timequantitative polymerase chain reaction (RT-qPCR) was used to detect the expression and overexpression level of lncRNA FAM138B (FAM138B) in cells and tissues. The CCK-8, Transwell migration and invasion methods were performed to observe the cell transfection.The interaction between FAM138B and miR-105-5p was predicted by the bioinformatics tool starBase v2.0, and verified by the luciferase reporter gene experiment. Kaplan-Meier and Cox regression analyses were used to determine the prognostic significance of FAM138B in NSCLC. The expression of FAM138B is down-regulated in NSCLC cells and tissues. Overexpression of FAM138B can inhibit the expression level of miR-105-5p in NSCLC cells, and the ability of NSCLC cells to proliferate, migrate and invade is downregulated. FAM138B targets miR-105-5p, and there is a negative correlation between FAM138B and miR-105-5p. It is confirmed that FAM138B inhibits the progression of NSCLC by targeting miR-105-5p and can be a potential prognostic biomarker for NSCLC.
作为一种肺癌,非小细胞肺癌(NSCLC)具有高死亡率和高复发率的特点,对人类的生命和健康构成了巨大威胁。由于手术治疗风险高,伤口恢复缓慢,非编码 RNA,尤其是长链非编码 RNA(lncRNAs)被用作新的潜在临床预后标志物,以提前预防和治疗癌症。本研究旨在探讨 FAM138B 在 NSCLC 中的作用及其作为预后生物标志物的可能性。实时定量聚合酶链反应(RT-qPCR)用于检测细胞和组织中 lncRNA FAM138B(FAM138B)的表达和过表达水平。CCK-8、Transwell 迁移和侵袭方法用于观察细胞转染。生物信息学工具 starBase v2.0 预测 FAM138B 与 miR-105-5p 的相互作用,并通过荧光素酶报告基因实验验证。Kaplan-Meier 和 Cox 回归分析用于确定 FAM138B 在 NSCLC 中的预后意义。FAM138B 在 NSCLC 细胞和组织中的表达下调。FAM138B 的过表达可抑制 NSCLC 细胞中 miR-105-5p 的表达水平,下调 NSCLC 细胞的增殖、迁移和侵袭能力。FAM138B 靶向 miR-105-5p,并且 FAM138B 和 miR-105-5p 之间存在负相关。证实 FAM138B 通过靶向 miR-105-5p 抑制 NSCLC 的进展,并且可以作为 NSCLC 的潜在预后生物标志物。