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电压门控钾离子通道分子Kv1.3在结直肠癌发生机制中的表观遗传调控

Epigenetic regulation of voltage-gated potassium ion channel molecule Kv1.3 in mechanisms of colorectal cancer.

作者信息

He Tao, Wang Can, Zhang Meiying, Zhang Xiaomei, Zheng Shufang, Linghu Enqiang, Guo Mingzhou

机构信息

Department of Gastroenterology and Hepatology, Chinese PLA General Hospital, Beijing 100853, China.

Department of Pathology, The Affiliated Hospital of Logistics University of Chinese People's Armed Police Force, Tianjin 300162, China.

出版信息

Discov Med. 2017 Mar;23(126):155-162.

Abstract

Colorectal cancer (CRC) is among the leading causes of cancer-related death throughout the world. Aberrant expression of voltage-gated potassium ion channel molecule Kv1.3 has been reported in various cancers. To explore the expression and regulation of Kv1.3 in colorectal cancer, 7 colorectal cancer cell lines and 147 cases of primary colorectal cancer were involved in this study. Kv1.3 was expressed in LOVO and SW480 cells and loss of expression was found in RKO, DLD1, SW620, HCT116, and HT29 cells. Complete methylation was found in RKO, DLD1, SW620, HCT116, and HT29 cells, partial methylation was found in LOVO and SW480 cells. Loss of/reduced expression of Kv1.3 is correlated with methylation of its promoter region. The expression of Kv1.3 was restored in RKO, DLD1, SW620, HCT116, and HT29 cells, and increased in LOVO and SW480 cells after 5-aza-2'-deoxycytidine (DAC) treatment. The results suggest that the expression of Kv1.3 is regulated by the gene's promoter region methylation in human CRC cells. Kv1.3 was methylated in 76.19% (112/147) of primary human colorectal cancer. Methylation of Kv1.3 is associated with age, tumor differentiation, and poor 5-year survival. In conclusion, Kv1.3 is frequently methylated in human colorectal cancer and the expression of Kv1.3 is regulated by its promoter region methylation. Kv1.3 methylation may serve as diagnostic and prognostic markers in colorectal cancer.

摘要

结直肠癌(CRC)是全球癌症相关死亡的主要原因之一。据报道,电压门控钾离子通道分子Kv1.3在多种癌症中存在异常表达。为了探究Kv1.3在结直肠癌中的表达及调控情况,本研究纳入了7种结直肠癌细胞系和147例原发性结直肠癌病例。Kv1.3在LOVO和SW480细胞中表达,而在RKO、DLD1、SW620、HCT116和HT29细胞中表达缺失。在RKO、DLD1、SW620、HCT116和HT29细胞中发现完全甲基化,在LOVO和SW480细胞中发现部分甲基化。Kv1.3表达缺失/降低与其启动子区域甲基化相关。用5-氮杂-2'-脱氧胞苷(DAC)处理后,RKO、DLD1、SW620、HCT116和HT29细胞中Kv1.3的表达得以恢复,LOVO和SW480细胞中的表达增加。结果表明,Kv1.3的表达在人结直肠癌细胞中受该基因启动子区域甲基化调控。在76.19%(112/147)的原发性人类结直肠癌中,Kv1.3发生甲基化。Kv1.3甲基化与年龄、肿瘤分化及5年生存率低相关。总之,Kv1.3在人类结直肠癌中频繁发生甲基化,其表达受启动子区域甲基化调控。Kv1.3甲基化可能作为结直肠癌的诊断和预后标志物。

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