Aberrant gene silencing in tumor progression: Implications for control of cancer

被引:42
作者
Baylin, S. B. [1 ]
Chen, W. Y. [1 ]
机构
[1] Sidney Kimmel Comprehens Canc Ctr John Hopkins, Baltimore, MD 21231 USA
来源
MOLECULAR APPROACHES TO CONTROLLING CANCER | 2005年 / 70卷
关键词
D O I
10.1101/sqb.2005.70.010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Although it is clear that genetic alterations are critical for the initiation and maintenance of human cancer, it is also becoming evident that epigenetic changes may be essential for the development of these diseases as well. The best studied of these latter processes is heritable transcriptional repression of genes associated with aberrant DNA hypermethylation of their promoters. Herein we review how very early occurrence of these gene silencing events may contribute to loss of key gene functions which result in disruption of cell regulatory pathways that may contribute to abnormal cell population expansion. These altered regulatory events may then provide a setting where mutations in the same disrupted pathways may be readily selected and serve to lock tumor progression into place. This hypothesis has potential impact on means to prevent and control cancer and for the use of epigenetic markers for cancer risk assessment and early diagnosis.
引用
收藏
页码:427 / 433
页数:7
相关论文
共 69 条
[61]   Stromal cells can contribute oncogenic signals [J].
Tlsty, TD .
SEMINARS IN CANCER BIOLOGY, 2001, 11 (02) :97-104
[62]  
Toyota M, 1999, CANCER RES, V59, P2307
[63]   Innovation - Detection and interpretation of altered methylation patterns in cancer cells [J].
Ushijima, T .
NATURE REVIEWS CANCER, 2005, 5 (03) :223-231
[64]   The polycomb group protein EZH2 is involved in progression of prostate cancer [J].
Varambally, S ;
Dhanasekaran, SM ;
Zhou, M ;
Barrette, TR ;
Kumar-Sinha, C ;
Sanda, MG ;
Ghosh, D ;
Pienta, KJ ;
Sewalt, RGAB ;
Otte, AP ;
Rubin, MA ;
Chinnaiyan, AM .
NATURE, 2002, 419 (6907) :624-629
[65]   hSIR2SIRT1 functions as an NAD-dependent p53 deacetylase [J].
Vaziri, H ;
Dessain, SK ;
Eagon, EN ;
Imai, SI ;
Frye, RA ;
Pandita, TK ;
Guarente, L ;
Weinberg, RA .
CELL, 2001, 107 (02) :149-159
[66]   P53 ACTIVATES EXPRESSION OF HIC-1, A NEW CANDIDATE TUMOR-SUPPRESSOR GENE ON 17P13.3 [J].
WALES, MM ;
BIEL, MA ;
ELDEIRY, W ;
NELKIN, BD ;
ISSA, P ;
CAVENEE, WK ;
KUERBITZ, SJ ;
BAYLIN, SB .
NATURE MEDICINE, 1995, 1 (06) :570-577
[67]   Cancer: Addiction to oncogenes - The Achilles heal of cancer [J].
Weinstein, IB .
SCIENCE, 2002, 297 (5578) :63-64
[68]   Pharmacologic unmasking of epigenetically silenced tumor suppressor genes in esophageal squamous cell carcinoma [J].
Yamashita, K ;
Upadhyay, S ;
Osada, M ;
Hoque, MO ;
Xiao, Y ;
Mori, M ;
Sato, F ;
Meltzer, SJ ;
Sidransky, D .
CANCER CELL, 2002, 2 (06) :485-495
[69]   Global assessment of promoter methylation in a mouse model of cancer identifies ID4 as a putative tumor-suppressor gene in human leukemia [J].
Yu, L ;
Liu, CH ;
Vandeusen, J ;
Becknell, B ;
Dai, ZY ;
Wu, YZ ;
Raval, A ;
Liu, TH ;
Ding, W ;
Mao, C ;
Liu, SJ ;
Smith, LT ;
Lee, S ;
Rassenti, L ;
Marcucci, G ;
Byrd, J ;
Caligiuri, MA ;
Plass, C .
NATURE GENETICS, 2005, 37 (03) :265-274