Department of General Surgery, The First Affiliated Hospital of Jinan University, Guangzhou, 510632, China.
College of Pharmacy, Jinan University, Guangzhou, 510632, China.
Int J Biol Sci. 2021 Apr 22;17(7):1757-1768. doi: 10.7150/ijbs.59001. eCollection 2021.
Long noncoding RNA KCNQ1 opposite strand/antisense transcript 1 (lncRNA KCNQ1OT1) is abnormally expressed in various solid tumors. The purpose of this study was to explore the prognostic value and potential functional role of lncRNA KCNQ1OT1 across cancers. We performed a meta-analysis of published literature to evaluate the prognostic value of lncRNA KCNQ1OT1 across cancers. Verification, functional analysis, and genomic variation analysis were performed using the GEPIA, TIMER, and LnCeVar databases. According to the immune cell infiltration level, we established a prognostic model of lncRNA KCNQ1OT1 expression using public datasets of TIMER. We used quantitative real-time polymerase chain reaction (RT-qPCR) and western blot to detect the expression levels of lncRNA KCNQ1OT1 and the CD155 protein in colorectal cancer (CRC) tissues and cell lines. Then, a lncRNA KCNQ1OT1-knockdown cell line was cocultured to explore the role of lncRNA KCNQ1OT1 and CD155 in the T cell response by flow cytometric analysis. Our results showed that the high expression of lncRNA KCNQ1OT1 was significantly related to poor overall survival across cancers, especially CRC. Interestingly, we found that COAD patients with high lncRNA KCNQ1OT1 expression and high CD8 T cell infiltration levels had a worse prognosis than those with low lncRNA KCNQ1OT1 expression and high CD8 T cell infiltration levels. Moreover, lncRNA KCNQ1OT1 and CD155 showed significantly higher expression in CRC tissue than in normal tissue, and lncRNA KCNQ1OT1 expression was positively correlated with CD155 expression in CRC. Finally, knockdown of lncRNA KCNQ1OT1 reduced CD155 expression in HCT116 and SW620 cells and enhanced the immune response in coculture with CD8 T cells. High lncRNA KCNQ1OT1 expression is significantly correlated with poor prognosis of CRC patients and mediates the CD8 T cell response in CRC. These findings indicate that lncRNA KCNQ1OT1 is a prognostic biomarker and potential immune therapeutic target for enhancing the CD8 T cell response in CRC.
长链非编码 RNA KCNQ1 反义链/反义转录本 1(lncRNA KCNQ1OT1)在各种实体瘤中异常表达。本研究旨在探讨 lncRNA KCNQ1OT1 在癌症中的预后价值和潜在功能作用。
我们对已发表的文献进行了荟萃分析,以评估 lncRNA KCNQ1OT1 在癌症中的预后价值。使用 GEPIA、TIMER 和 LnCeVar 数据库进行验证、功能分析和基因组变异分析。根据免疫细胞浸润水平,我们使用 TIMER 的公共数据集建立了 lncRNA KCNQ1OT1 表达的预后模型。我们使用实时定量聚合酶链反应(RT-qPCR)和蛋白质印迹法检测结直肠癌(CRC)组织和细胞系中 lncRNA KCNQ1OT1 和 CD155 蛋白的表达水平。然后,通过流式细胞术分析共培养敲低 lncRNA KCNQ1OT1 的细胞系,以探讨 lncRNA KCNQ1OT1 和 CD155 在 T 细胞反应中的作用。
我们的结果表明,lncRNA KCNQ1OT1 的高表达与癌症尤其是 CRC 的总体生存率差显著相关。有趣的是,我们发现 COAD 患者中 lncRNA KCNQ1OT1 高表达且 CD8 T 细胞浸润水平高的患者预后比 lncRNA KCNQ1OT1 低表达且 CD8 T 细胞浸润水平高的患者更差。此外,CRC 组织中 lncRNA KCNQ1OT1 和 CD155 的表达明显高于正常组织,CRC 中 lncRNA KCNQ1OT1 的表达与 CD155 的表达呈正相关。最后,敲低 lncRNA KCNQ1OT1 降低了 HCT116 和 SW620 细胞中 CD155 的表达,并增强了与 CD8 T 细胞共培养中的免疫反应。
高 lncRNA KCNQ1OT1 表达与 CRC 患者的不良预后显著相关,并介导 CRC 中 CD8 T 细胞的反应。这些发现表明,lncRNA KCNQ1OT1 是 CRC 患者的预后生物标志物和潜在的免疫治疗靶点,可增强 CRC 中 CD8 T 细胞的反应。