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启动子甲基化导致结直肠癌中B细胞易位基因1表达下调

Down-regulation of B-Cell Translocation Gene 1 by Promoter Methylation in Colorectal Carcinoma.

作者信息

Jung Yoon Yang, Sung Ji-Youn, Kim Ji-Ye, Kim Hyun-Soo

机构信息

Department of Pathology, Myongji Hospital, Goyang, Republic of Korea.

Department of Pathology, Kyung Hee University School of Medicine, Seoul, Republic of Korea.

出版信息

Anticancer Res. 2018 Feb;38(2):691-697. doi: 10.21873/anticanres.12274.

Abstract

BACKGROUND

B-cell translocation gene 1 (BTG1) acts as a tumour suppressor in human malignancies. However, the precise mechanism of BTG1 down-regulation in colorectal carcinoma (CRC) remains unclear. We analyzed BTG1 expression in CRC cell lines and tissues and investigated the mechanism underlying the observed alterations.

MATERIALS AND METHODS

Real-time polymerase chain reaction (PCR) and western blot analyses were performed to analyze BTG1 expression in CRC cell lines. The methylation status of the BTG1 promoter region in cell lines was determined by methylation-specific PCR, and the effect of demethylation on BTG1 expression was explored with 5-aza-deoxycytidine treatment. BTG1 protein expression in CRC tissue samples was evaluated using immunostaining.

RESULTS

CRC cell lines and tissue samples expressed lower levels of BTG1 compared to controls, and BTG1 levels were significantly lower in metastatic than primary CRC. In BTG1-down-regulated CRC cell lines, the BTG1 promoter was highly methylated, and 5-aza-deoxycytidine significantly restored BTG1 expression.

CONCLUSION

BTG1 down-regulation in CRC occurs through epigenetic repression, which is involved in the development and progression of CRC.

摘要

背景

B细胞易位基因1(BTG1)在人类恶性肿瘤中作为一种肿瘤抑制因子发挥作用。然而,结直肠癌(CRC)中BTG1下调的确切机制仍不清楚。我们分析了CRC细胞系和组织中BTG1的表达,并研究了所观察到的改变背后的机制。

材料与方法

进行实时聚合酶链反应(PCR)和蛋白质免疫印迹分析以分析CRC细胞系中BTG1的表达。通过甲基化特异性PCR确定细胞系中BTG1启动子区域的甲基化状态,并通过5-氮杂脱氧胞苷处理探究去甲基化对BTG1表达的影响。使用免疫染色评估CRC组织样本中BTG1蛋白的表达。

结果

与对照相比,CRC细胞系和组织样本中BTG1的表达水平较低,并且转移型CRC中BTG1水平显著低于原发性CRC。在BTG1下调的CRC细胞系中,BTG1启动子高度甲基化,5-氮杂脱氧胞苷显著恢复了BTG1的表达。

结论

CRC中BTG1的下调通过表观遗传抑制发生,这与CRC的发生和发展有关。

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