Tu Jing, Tang Min, Li Guoqing, Chen Liang, Wang Yubo, Huang Yong
Department of Pulmonary and Critical Care Medicine, Chongqing General Hospital, No. 118, Xingguang Avenue, Liangjiang New Area, Chongqing 401147, China.
Department of Oncology, Chongqing General Hospital, No. 118, Xingguang Avenue, Liangjiang New Area, Chongqing 401147, China.
J Oncol. 2022 Aug 26;2022:4181658. doi: 10.1155/2022/4181658. eCollection 2022.
Lung cancer is still the major contributor to cancer-related mortality. Over 85% of patients suffer from non-small-cell lung cancer (NSCLC). Mucins (MUCs) are large glycoproteins secreted or membrane-bound produced by epithelial cells in normal and malignant tissues. They are the major components of the mucous gel that covers the surface of the respiratory epithelium. Certain MUCs have been used or proposed to act as biomarkers for lung cancer. Nevertheless, the expression, messenger ribonucleic acid (mRNA) levels, and the prognostic value of MUCs in NSCLC are yet to be investigated systematically. In this research, the biological information of MUC proteins in patients with NSCLC was examined using a series of databases. The results based on gene expression profiling interactive analysis (GEPIA) illustrated that the expression and mRNAs was remarkably upmodulated in lung adenocarcinoma (LUAD) patients, whereas the expression was downregulated in lung squamous cell carcinoma (LUSC) patients. Kaplan-Meier plotter (KM Plotter) analysis revealed that elevated mRNA expression levels of and were linked to unfavourable overall survival (OS) in NSCLC, while increased mRNA expression of and was linked to good OS, especially in LUAD patients. In addition, differential expression of , , , , , and mRNA was linked to the prognoses of NSCLC patients with varied clinical-pathological subtypes. Genetic alterations of MUCs in NSCLC primarily involved mutations, fusion, amplification, deep deletion, and multiple alterations according to cancer genomics (cBioPortal). Therefore, we propose that combinations of MUC proteins can act as prognostic biomarkers and demonstrate the therapeutic potential for NSCLC-related therapy.
肺癌仍然是癌症相关死亡的主要原因。超过85%的患者患有非小细胞肺癌(NSCLC)。粘蛋白(MUCs)是正常组织和恶性组织中上皮细胞分泌的或膜结合的大型糖蛋白。它们是覆盖呼吸道上皮表面的粘液凝胶的主要成分。某些MUCs已被用于或被提议作为肺癌的生物标志物。然而,MUCs在NSCLC中的表达、信使核糖核酸(mRNA)水平及其预后价值尚未得到系统研究。在本研究中,我们使用一系列数据库检查了NSCLC患者中MUC蛋白的生物学信息。基于基因表达谱交互式分析(GEPIA)的结果表明,在肺腺癌(LUAD)患者中,MUC蛋白的表达和mRNA水平显著上调,而在肺鳞状细胞癌(LUSC)患者中表达下调。Kaplan-Meier绘图仪(KM Plotter)分析显示,在NSCLC中,某些MUCs的mRNA表达水平升高与不良总生存期(OS)相关,而另外一些MUCs的mRNA表达增加与良好的OS相关,尤其是在LUAD患者中。此外,某些MUCs的mRNA差异表达与不同临床病理亚型的NSCLC患者的预后相关。根据癌症基因组学(cBioPortal),NSCLC中MUCs的基因改变主要包括突变、融合、扩增、深度缺失和多种改变。因此,我们提出MUC蛋白组合可作为预后生物标志物,并显示出NSCLC相关治疗的潜力。