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
[51]   A family of secreted proteins contains homology to the cysteine-rich ligand-binding domain of frizzled receptors [J].
Rattner, A ;
Hsieh, JC ;
Smallwood, PM ;
Gilbert, DJ ;
Copeland, NG ;
Jenkins, NA ;
Nathans, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (07) :2859-2863
[52]   Normal human mammary epithelial cells spontaneously escape senescence and acquire genomic changes [J].
Romanov, SR ;
Kozakiewicz, BK ;
Holst, CR ;
Stampfer, MR ;
Haupt, LM ;
Tlsty, TD .
NATURE, 2001, 409 (6820) :633-637
[53]  
Salem CE, 2000, INT J CANCER, V87, P179, DOI 10.1002/1097-0215(20000715)87:2<179::AID-IJC4>3.0.CO
[54]  
2-X
[55]   A PORTABLE SIGNAL CAUSING FAITHFUL DNA METHYLATION DENOVO IN NEUROSPORA-CRASSA [J].
SELKER, EU ;
JENSEN, BC ;
RICHARDSON, GA .
SCIENCE, 1987, 238 (4823) :48-53
[56]  
Shi HD, 2003, CANCER RES, V63, P2164
[57]   Epigenetic inactivation of SFRP genes allows constitutive WNT signaling in colorectal cancer [J].
Suzuki, H ;
Watkins, DN ;
Jair, KW ;
Schuebel, KE ;
Markowitz, SD ;
Chen, WD ;
Pretlow, TP ;
Bin Yang, ;
Akiyama, Y ;
van Engeland, M ;
Toyota, M ;
Tokino, T ;
Hinoda, Y ;
Imai, K ;
Herman, JG ;
Baylin, SB .
NATURE GENETICS, 2004, 36 (04) :417-422
[58]   A genomic screen for genes upregulated by demethylation and histone deacetylase inhibition in human colorectal cancer [J].
Suzuki, H ;
Gabrielson, E ;
Chen, W ;
Anbazhagan, R ;
van Engeland, M ;
Weijenberg, MP ;
Herman, JG ;
Baylin, SB .
NATURE GENETICS, 2002, 31 (02) :141-149
[59]   A histone H3 methyltransferase controls DNA methylation in Neurospora crassa [J].
Tamaru, H ;
Selker, EU .
NATURE, 2001, 414 (6861) :277-283
[60]   Synthesis of signals for De Novo DNA methylation in Neurospora crassa [J].
Tamaru, H ;
Selker, EU .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (07) :2379-2394