Hou Guoxin, Lu Zhimin, Bi Yanyu, Deng Jingjing, Yang Xinmei
Department of Oncology, The First Hospital of Jiaxing, Affiliated Hospital of Jiaxing University, Jiaxing, Zhejiang, China.
Department of Outpatient, The First Hospital of Jiaxing, Affiliated Hospital of Jiaxing University, Jiaxing, Zhejiang, China.
Med Oncol. 2022 Feb 12;39(5):51. doi: 10.1007/s12032-022-01654-7.
Non-small cell lung carcinoma (NSCLC) accounts for the majority of lung cancer which is one of the most common cancer types and results in high percentage of cancer-related deaths. Although NSCLC patients have been benefiting from the existing standard treatments, more candidate biomarkers for effective diagnosis and targets for therapy are still required to be uncovered. The expression pattern and biological function of Excision repair cross-complementation group 6 like (ERCC6L) in NSCLC are ill-investigated.
We performed bioinformatic analyses in NSCLC patients with lung adenocarcinoma (LUAD) or lung squamous cell carcinoma (LUSC), respectively. Patient survival determination and meta-analysis were carried out to check the clinical significance of ERCC6L. Datamining was also performed to evaluate the ERCC6L mRNA and protein expression levels in patients with LUAD and the correlation with immune cell infiltration. In silico prediction indicated the potential interacting proteins and correlated pathways of ERCC6L in LUAD. Loss-of-function studies were performed to determine the role of ERCC6L in LUAD cells.
Here, we found that ERCC6L is upregulated in patients with LUAD and LUSC and is strongly associated with poor outcomes of LUAD, but not LUSC, patients. In addition, ERCC6L mRNA and protein were shown to be more expressed in patients with advanced stages of LUAD. Finally, functional analyses reveal the promoting effects of ERCC6L on LUAD cell survival, migration and invasion.
Cohort data analysis and experimental validation shed light on the promising prognostic and therapeutic application of ERCC6L in LUAD, but maybe not LUSC, patients.
非小细胞肺癌(NSCLC)占肺癌的大多数,肺癌是最常见的癌症类型之一,导致与癌症相关的高死亡率。尽管NSCLC患者已从现有的标准治疗中受益,但仍需要发现更多用于有效诊断的候选生物标志物和治疗靶点。切除修复交叉互补组6样蛋白(ERCC6L)在NSCLC中的表达模式和生物学功能研究不足。
我们分别对肺腺癌(LUAD)或肺鳞状细胞癌(LUSC)的NSCLC患者进行了生物信息学分析。进行患者生存判定和荟萃分析以检查ERCC6L的临床意义。还进行了数据挖掘以评估LUAD患者中ERCC6L mRNA和蛋白表达水平以及与免疫细胞浸润的相关性。计算机模拟预测表明了LUAD中ERCC6L的潜在相互作用蛋白和相关途径。进行功能丧失研究以确定ERCC6L在LUAD细胞中的作用。
在此,我们发现ERCC6L在LUAD和LUSC患者中上调,并且与LUAD患者(而非LUSC患者)的不良预后密切相关。此外,ERCC6L mRNA和蛋白在LUAD晚期患者中表达更高。最后,功能分析揭示了ERCC6L对LUAD细胞存活、迁移和侵袭的促进作用。
队列数据分析和实验验证揭示了ERCC6L在LUAD患者(可能不适用于LUSC患者)中有前景的预后和治疗应用。