Epigenetic regulation of mucin genes in human cancers.

Epigenetic regulation of mucin genes in human cancers.
复制标题

DOI:
10.1007/s13148-011-0037-3
复制
发表时间:
2011-08
影响因子:
5.7
通讯作者:
Yonezawa, Suguru
Yonezawa, Suguru
中科院分区:
医学1区
文献类型:
--
作者:
Yamada, Norishige;Kitamoto, Sho;Yokoyama, Seiya;Hamada, Tomofumi;Goto, Masamichi;Tsutsumida, Hideaki;Higashi, Michiyo;Yonezawa, Suguru

文献摘要

参考文献

被引文献

相似文献

粘蛋白是高分子量糖蛋白,在诊断和预后预测以及癌发生和肿瘤侵袭中发挥重要作用。粘蛋白基因表达的调节已被广泛研究,并且已经描述了启动子区域的信号通路、转录调节因子和表观遗传修饰。检测癌症相关粘蛋白基因的表观遗传状态对于癌症的早期诊断以及监测肿瘤行为和对靶向治疗的反应非常重要。 micro-RNA 对粘蛋白基因表达的影响也开始显现。在这篇综述中,我们讨论了目前对粘蛋白基因(MUC1、MUC2、MUC3A、MUC4、MUC5AC、MUC5B、MUC6、MUC16和MUC17)调控的表观遗传机制的观点以及该表观遗传信息可能的临床应用。
Mucins are high molecular weight glycoproteins that play important roles in diagnostic and prognostic prediction and in carcinogenesis and tumor invasion. Regulation of expression of mucin genes has been studied extensively, and signaling pathways, transcriptional regulators, and epigenetic modification in promoter regions have been described. Detection of the epigenetic status of cancer-related mucin genes is important for early diagnosis of cancer and for monitoring of tumor behavior and response to targeted therapy. Effects of micro-RNAs on mucin gene expression have also started to emerge. In this review, we discuss the current views on epigenetic mechanisms of regulation of mucin genes (MUC1, MUC2, MUC3A, MUC4, MUC5AC, MUC5B, MUC6, MUC16, and MUC17) and the possible clinical applications of this epigenetic information.
DOI: 10.1093/humrep/10.1.98
发表时间: 1995-01-01
期刊: HUMAN REPRODUCTION
影响因子: 6.1
作者:
AUDIE, JP;TETAERT, D;BOERSMA, A
通讯作者: BOERSMA, A
DOI: 10.1074/jbc.272.6.3168
发表时间: 1997-02-07
影响因子: 4.8
作者:
Desseyn, JL;GuyonnetDuperat, V;Laine, A
通讯作者: Laine, A
DOI: 10.1002/jcb.22116
发表时间: 2009-05-01
影响因子: 4
作者:
Fullwood, Melissa J.;Ruan, Yijun
通讯作者: Ruan, Yijun
DOI: 10.1007/pl00006276
发表时间: 1998-01-01
影响因子: 3.9
作者:
Desseyn, JL;Buisine, MP;Laine, A
通讯作者: Laine, A
DOI: 10.1095/biolreprod60.1.58
发表时间: 1999-01-01
影响因子: 3.6
作者:
Gipson, IK;Spurr-Michaud, S;Hill, JA
通讯作者: Hill, JA