3.8 Review

Mechanisms of Disease: methyl-binding domain proteins as potential therapeutic targets in cancer

期刊

NATURE CLINICAL PRACTICE ONCOLOGY
卷 4, 期 5, 页码 305-315

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/ncponc0812

关键词

Kaiso; MBD2; MBD4; MeCP2; methyl-binding domain

类别

资金

  1. Medical Research Council [G0301154] Funding Source: Medline
  2. MRC [G0301154] Funding Source: UKRI
  3. Medical Research Council [G0301154] Funding Source: researchfish

向作者/读者索取更多资源

The methyl-CpG-binding domain (MBD) proteins 'read' and interpret the methylation moieties on DNA, and thus are critical mediators of many epigenetic processes. Currently, the MBD family comprises five members; MBD1, MBD2, MBD3, MBD4 and MeCP2. Although not a 'classical' MBD protein, Kaiso also mediates transcriptional repression by using zinc finger domains to bind its targets. Since DNA hypermethylation is a well-recognized mechanism underlying gene silencing events in both tumorigenesis and drug resistance, it is likely that the MBD proteins may be important modulators of tumorigenesis. We review the recent work addressing this possibility, and discuss several of the MBD proteins as potentially excellent novel therapeutic targets.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

3.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据