He Junming, Fu Yin, Hu Jiangwei, Chen Jian, Lou Guoliang
Department of Cardiothoracic Surgery, Yiwu Central Hospital, Yiwu, 322000, People's Republic of China.
Cancer Manag Res. 2021 Jun 30;13:5177-5185. doi: 10.2147/CMAR.S304869. eCollection 2021.
Studies have indicated that AGR2 is crucial in many cancers. However, its methylation level in lung adenocarcinoma (LUAD) is rarely known. Hence, the effect of AGR2 methylation on LUAD was explored in the study.
qRT-PCR was adopted to detect the expression of AGR2 in LUAD cells and normal lung cells. Methylation-specific PCR (MSP) was used to detect the methylation of AGR2 promoter region in different cell lines. MTT, Transwell and wound healing assays were used to verify the progression of cells in each transfection group.
The expression of AGR2 was significantly up-regulated in LUAD cells relative to that in normal cells. Moreover, the expression of AGR2 was inversely modulated by DNA methylation, and the hypomethylation of CpG islands would lead to the increased expression of AGR2. Finally, overexpression and hypomethylation of AGR2 facilitated the proliferation, invasion and migration of LUAD cells.
These results demonstrated that hypomethylation of AGR2 promoter region promoted the expression of AGR2 in LUAD cells, thus promoting the progression of LUAD cells.
研究表明AGR2在多种癌症中至关重要。然而,其在肺腺癌(LUAD)中的甲基化水平鲜为人知。因此,本研究探讨了AGR2甲基化对LUAD的影响。
采用qRT-PCR检测AGR2在LUAD细胞和正常肺细胞中的表达。甲基化特异性PCR(MSP)用于检测不同细胞系中AGR2启动子区域的甲基化情况。MTT、Transwell和伤口愈合试验用于验证各转染组细胞的进展。
与正常细胞相比,AGR2在LUAD细胞中的表达显著上调。此外,AGR2的表达受到DNA甲基化的反向调节,CpG岛的低甲基化会导致AGR2表达增加。最后,AGR2的过表达和低甲基化促进了LUAD细胞的增殖、侵袭和迁移。
这些结果表明,AGR2启动子区域的低甲基化促进了LUAD细胞中AGR2的表达,从而促进了LUAD细胞的进展。