5' CPG ISLAND METHYLATION IS ASSOCIATED WITH TRANSCRIPTIONAL SILENCING OF THE TUMOR-SUPPRESSOR P16/CDKN2/MTS1 IN HUMAN CANCERS

被引:1765
作者
MERLO, A
HERMAN, JG
MAO, L
LEE, DJ
GABRIELSON, E
BURGER, PC
BAYLIN, SB
SIDRANSKY, D
机构
[1] JOHNS HOPKINS UNIV,SCH MED,DEPT OTOLARYNGOL,DIV HEAD & NECK CANC RES,BALTIMORE,MD 21205
[2] JOHNS HOPKINS ONCOL CTR,BALTIMORE,MD 21231
[3] JOHNS HOPKINS MED INST,DEPT PATHOL,BALTIMORE,MD 21287
关键词
D O I
10.1038/nm0795-686
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
Loss of heterozygosity on chromosome 9p21 is one of the most frequent genetic: alterations identified in human cancer. The rate of point mutations of p16, a candidate suppressor gene of this area, is low in most primary tumours with allelic loss of 9p21. Monosomic cell lines with structurally unaltered p16 show methylation of the 5' CpG island of p16. This distinct methylation pattern was associated with a complete transcriptional block that was reversible upon treatment with 5-deoxyazacytidine. Moreover, de novo methylation of the 5' CpG island of p16 was also found in approximately 20% of different primary neoplasms, but not in normal tissues, potentially representing a common pathway of tumour suppressor gene inactivation in human cancers.
引用
收藏
页码:686 / 692
页数:7
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