Correlation and clinical significance of methyltransferases SETDB1 and SPG20 methylation in lung adenocarcinoma

Zongying Liang, Bao-Hui Zhao, Jingtao Huang
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Abstract

Objective: The incidence of primary lung adenocarcinoma is increasing year by year in worldwide, and it has surpassed squamous cell carcinoma to become the most common pathological type of lung cancer. Advances in medical technology have made the overall survival rate of lung cancer patients improve, but it is still very low. In the study, we investigated the methyltransferase SETDB1 expression and the methylation level of SPG20, and analyzed the correlation and its clinical significance in the pathogenesis of lung adenocarcinoma. Methods: 60 lung adenocarcinoma and normal lung tissues were selected.The expression of SPG20 and SETDB1 mRNA was examined by RT-qPCR; Protein expression of SPG20 and SETDB1 was determined by immunohistochemistry(SP) and immune protein imprinting(Western blot);Methylation level of SPG20 gene was determined by pyrosequencing. Correlation between SETDB1 and SPG20 methylation levels and both and clinical case characteristics was analysed by statistics. Western blot detection of SETDB1 and SPG20 protein expression in lung adenocarcinoma cells and normal bronchial mucosal epithelial cells.The small interfering RNA of SETDB1 was transfected into lung adenocarcinoma A549 cells by liposome-mediated method, the mRNA and protein expression levels of SETDB1 were detected by RT-qPCR and Wesrern blot, and the methylation level of SPG20 gene was detected by pyrosequencing. Results:Relative expression of SPG20 mRNA was significantly lower in lung adenocarcinoma tissue than in normal lung tissue, while relative SETDB1 mRNA expression was higher in cancer tissue than in normal lung tissue. SETDB1 protein expression was significantly higher in lung adenocarcinoma tissue than in normal lung tissue, while SPG20 protein showed lower expression in cancer tissue than in normal lung tissue. The methylation rate of the SPG20 gene was significantly higher in cancerous tissues than in normal lung tissue, the difference was statistically significant. SPG20 methylation in cancer tissues showed a correlation with SETDB1 and showed a positive correlation; SPG20 methylation and SETDB1 are closely related with TNM stage, tissue differentiation, and lymph node metastasis in lung adenocarcinoma. The vitro experiments showed that SETDB1 was highly expressed, while SPG20 was lowIn lung adenocarcinoma cells, SETDB1 was low and SPG20 was high in normal bronchial epithelial cells. RNA interference with SETDB1 could significantly reduce the mRNA and protein expression of SETDB1 in A549 cells, the methylation rate of SPG20 gene was significantly decreased, and the protein expression was increased. Conclusion:There is a significant correlation between methyltransferases SETDB1 and SPG20 methylation in lung adenocarcinoma, and high SETDB1 expression may be the upstream molecule of SPG20 methylation, working together in promoting the occurrence and development of lung adenocarcinoma.
甲基转移酶SETDB1和sp20甲基化与肺腺癌的相关性及临床意义
目的:原发性肺腺癌在世界范围内的发病率呈逐年上升趋势,已超过鳞状细胞癌成为肺癌最常见的病理类型。医疗技术的进步使肺癌患者的总体生存率有所提高,但仍然很低。本研究通过研究甲基转移酶SETDB1的表达与SPG20的甲基化水平,分析二者在肺腺癌发病机制中的相关性及其临床意义。方法:选择肺腺癌和正常肺组织60例。RT-qPCR检测sp20和SETDB1 mRNA的表达;采用免疫组织化学(SP)和免疫蛋白印迹(Western blot)检测SPG20和SETDB1的蛋白表达;采用焦磷酸测序(pyrosequencing)检测SPG20基因的甲基化水平。统计学分析SETDB1和SPG20甲基化水平与两者及临床病例特征的相关性。Western blot检测肺腺癌细胞和正常支气管粘膜上皮细胞中SETDB1和SPG20蛋白的表达。采用脂质体介导法将SETDB1小干扰RNA转染肺腺癌A549细胞,RT-qPCR和Wesrern blot检测SETDB1 mRNA和蛋白表达水平,焦磷酸测序检测SPG20基因甲基化水平。结果:SPG20 mRNA在肺腺癌组织中的相对表达量明显低于正常肺组织,而SETDB1 mRNA在肺腺癌组织中的相对表达量明显高于正常肺组织。SETDB1蛋白在肺腺癌组织中的表达明显高于正常肺组织,而SPG20蛋白在癌组织中的表达明显低于正常肺组织。SPG20基因在癌组织中的甲基化率明显高于正常肺组织,差异有统计学意义。癌组织中sp20甲基化与SETDB1呈正相关;SPG20甲基化和SETDB1与肺腺癌TNM分期、组织分化、淋巴结转移密切相关。体外实验显示,SETDB1在肺腺癌细胞中高表达,而SPG20低表达,在正常支气管上皮细胞中低表达,SPG20高表达。RNA干扰SETDB1可显著降低A549细胞中SETDB1 mRNA和蛋白的表达,SPG20基因甲基化率显著降低,蛋白表达升高。结论:甲基转移酶SETDB1与SPG20甲基化在肺腺癌中存在显著相关性,SETDB1的高表达可能是SPG20甲基化的上游分子,共同促进肺腺癌的发生发展。
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