Epigenetic disruption of the WNT/β-catenin signaling pathway in human cancers

被引:164
|
作者
Ying, Ying
Tao, Qian
机构
[1] Chinese Univ Hong Kong, Canc Epigenet Lab, State Key Lab Oncol S China,Hong Kong Canc Inst, Sir YK Pao Ctr Canc,Dept Clin Oncol, Shatin, Hong Kong, Peoples R China
[2] Chinese Univ Hong Kong, Li Ka Shing Inst Hlth Sci, Shatin, Hong Kong, Peoples R China
关键词
cancer; WNT; beta-catenin; signaling; epigenetic; methylation; tumor suppressor; INHIBITORY FACTOR-I; FRIZZLED-RELATED PROTEIN; WNT ANTAGONIST SFRP1; BETA-CATENIN; COLORECTAL-CANCER; PROMOTER HYPERMETHYLATION; UP-REGULATION; ABERRANT METHYLATION; TUMOR-SUPPRESSOR; GROWTH-FACTOR;
D O I
10.4161/epi.4.5.9371
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Aberrant activation of the WNT/beta-catenin signaling pathway is frequently involved in a broad spectrum of human malignancies. Alternative to genetic deletions and point mutations, epigenetic inactivation of negative WNT regulators, through DNA methylation of promoter CpG islands and/or histone modification, leads to the activation or amplification of aberrant WNT/beta-catenin signaling. In this review, we summarized the contribution of epigenetic dysregulation of WNT/beta-catenin signaling to tumorigenesis and highlighted the importance of epigenetic identification of negative regulators of this pathway as putative tumor suppressors. The reversal of these silenced regulators may be developed as potential cancer therapeutics.
引用
收藏
页码:307 / 312
页数:6
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