Yang S Y, Zhu L H, Yang R, Liao T T, Hu X W
Department of Respiratory and Critical Care Medicine, the Affiliated Hospital of Guizhou Medical University, Guizhou 550000, China.
Guizhou Medical University, GuiZhou 550000, China.
Zhonghua Jie He He Hu Xi Za Zhi. 2023 Jun 12;46(6):580-586. doi: 10.3760/cma.j.cn112147-20220712-00596.
To investigate the role and mechanism of COL11A1 in lung adenocarcinoma migration and invasion. Surgical pathological tissues of 4 patients with lung adenocarcinoma admitted to the Affiliated Hospital of Guizhou Medical University from September to November 2020 were used. Immunohistochemical methods were used to identify lung adenocarcinoma tissues, para-cancerous tissues and parallel transcriptome sequencing. Genetic prognostic analysis was conducted by TCGA and GTEx databases.The expression level of COL11A1 gene in lung adenocarcinoma and adjacent tissues was detected by Western blotting.The primary human lung adenocarcinoma cells cultured. The COL11A1 siRNA was transfected into primary human lung adenocarcinoma cells, then the transcriptome sequencing of differential genes was performed,and KEGG enrichment analysis of differential gene enrichment pathway was conducted. Protein expression and phosphorylation were detected by Western blot method. Cell migration was detected by scratch healing test. Cell proliferation was detected by CCK8 method and invasion ability was detected by Transwell method. Ten differentially expressed genes were screened by transcription sequencing in lung adenocarcinoma. Prognostic analysis of single gene showed that COL11A1 gene expression level was correlated with survival rate (<0.001). The expression of COL11A1 in lung adenocarcinoma was higher than that in adjacent tissues by Western blot (<0.001). Transcriptome sequencing of COL11A1 siRNA transfection into primary human lung adenocarcinoma cells showed that differential genes were concentrated in PI3K-akt pathway. The expression of tumor suppressor gene PTEN in siRNA transfection group was significantly higher than that in control group and negative transfection group by Western blot. The expression of Aktp-Akt 473 p-Akt 308 p-PTENp-PDK1p-c-Rafp-GSK-3 β was down-regulated (all <0.05).Compared with the negative control group, the ability of migration, proliferation and invasion of primary human lung adenocarcinoma cells in siRNA transfection group decreased (all <0.05). COL11A1 regulates PI3K/Akt/GSK-3 β pathway to promote migration and invasion of primary human lung adenocarcinoma cells. COL11A1 regulates PI3K/Akt/GSK-3 β pathway to promote migration and invasion of primary human lung adenocarcinoma cells.
探讨COL11A1在肺腺癌迁移和侵袭中的作用及机制。采用贵州医科大学附属医院2020年9月至11月收治的4例肺腺癌患者的手术病理组织。运用免疫组织化学方法鉴定肺腺癌组织、癌旁组织并进行平行转录组测序。通过TCGA和GTEx数据库进行遗传预后分析。采用蛋白质免疫印迹法检测肺腺癌及癌旁组织中COL11A1基因的表达水平。培养原代人肺腺癌细胞。将COL11A1 siRNA转染至原代人肺腺癌细胞,随后进行差异基因的转录组测序,并对差异基因富集通路进行KEGG富集分析。采用蛋白质免疫印迹法检测蛋白质表达及磷酸化水平。通过划痕愈合试验检测细胞迁移能力。采用CCK8法检测细胞增殖能力,采用Transwell法检测细胞侵袭能力。通过转录测序筛选出肺腺癌中10个差异表达基因。单基因预后分析显示,COL11A1基因表达水平与生存率相关(<0.001)。蛋白质免疫印迹法检测结果显示,COL11A1在肺腺癌中的表达高于癌旁组织(<0.001)。对转染COL11A1 siRNA的原代人肺腺癌细胞进行转录组测序,结果显示差异基因集中在PI3K-akt通路。蛋白质免疫印迹法检测结果显示,siRNA转染组中抑癌基因PTEN的表达显著高于对照组和阴性转染组。Aktp-Akt 473、p-Akt 308、p-PTEN、p-PDK1、p-c-Raf、p-GSK-3β的表达下调(均<0.05)。与阴性对照组相比,siRNA转染组中原代人肺腺癌细胞的迁移、增殖和侵袭能力下降(均<0.05)。COL11A1通过调节PI3K/Akt/GSK-3β通路促进原代人肺腺癌细胞的迁移和侵袭。COL11A1通过调节PI3K/Akt/GSK-3β通路促进原代人肺腺癌细胞的迁移和侵袭。