The ATM gene is a target for epigenetic silencing in locally advanced breast cancer

被引:85
作者
Vo, QN
Kim, WJ
Cvitanovic, L
Boudreau, DA
Ginzinger, DG
Brown, KD
机构
[1] Dept Biochem & Mol Biol, New Orleans, LA USA
[2] LSU Hlth Sci Ctr, Stanley S Scott Canc Ctr, New Orleans, LA USA
[3] Dept Surg, New Orleans, LA USA
[4] Dept Pathol, New Orleans, LA USA
[5] Univ Calif San Francisco, UCSF Comprehens Canc Ctr, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
ATM; epigenetics; promoter hypermethylation; breast cancer;
D O I
10.1038/sj.onc.1208092
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
Several epidemiological studies on ataxia-telangiectasia families indicate that obligate ATM heterozygotes display an elevated risk for developing breast cancer. However, a molecular basis for a potential link between diminished ATM function and sporadic breast malignancy remains elusive. Here, we show that 78% (18 out of a panel of 23) of surgically removed breast tumors (stage II or greater) displayed aberrant methylation of the ATM proximal promoter region as judged by methylation-specific PCR. Aberrant methylation of the ATM promoter was independently confirmed in several tumors by bisulfate sequencing. Moreover, bisulfate sequencing indicated that this region of the genome is subject to dense methylation. Further, we found a highly significant correlation (P = 0.0006) between reduced ATM mRNA abundance, as measured by real-time RT-PCR, and aberrant methylation of the ATM gene promoter. These findings indicate that epigenetic silencing of ATM expression occurs in locally advanced breast tumors, and establish a link at the molecular level between reduced ATM function and sporadic breast malignancy.
引用
收藏
页码:9432 / 9437
页数:6
相关论文
共 22 条
[1]   Ataxia-telangiectasia-mutated (ATM) gene in head and neck squamous cell carcinoma:: Promoter hypermethylation with clinical correlation in 100 cases [J].
Ai, LB ;
Quynh, NV ;
Zuo, CL ;
Li, LW ;
Ling, WH ;
Suen, JY ;
Hanna, E ;
Brown, KD ;
Fan, CY .
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2004, 13 (01) :150-156
[2]  
Angèle S, 2000, CLIN CANCER RES, V6, P3536
[3]   Molecular genotyping shows that ataxia-telangiectasia heterozygotes are predisposed to breast cancer [J].
Athma, P ;
Rappaport, R ;
Swift, M .
CANCER GENETICS AND CYTOGENETICS, 1996, 92 (02) :130-134
[4]   Absence of mutations in the ATM gene in forty-seven cases of sporadic breast cancer [J].
Bebb, DG ;
Yu, Z ;
Chen, J ;
Telatar, M ;
Gelmon, K ;
Phillips, N ;
Gatti, RA ;
Glickman, BW .
BRITISH JOURNAL OF CANCER, 1999, 80 (12) :1979-1981
[5]   ATM variants 7271T>G and IVS10-6T>G among women with unilateral and bilateral breast cancer [J].
Bernstein, JL ;
Bernstein, L ;
Thompson, WD ;
Lynch, CF ;
Malone, KE ;
Teitelbaum, SL ;
Olsen, JH ;
Anton-Culver, H ;
Boice, JD ;
Rosenstein, BS ;
Borresen-Dale, AL ;
Gatti, RA ;
Concannon, P ;
Haile, RW .
BRITISH JOURNAL OF CANCER, 2003, 89 (08) :1513-1516
[6]   A gene transcribed from the bidirectional ATM promoter coding for a serine rich protein: Amino acid sequence, structure and expression studies [J].
Byrd, PJ ;
Cooper, PR ;
Stankovic, T ;
Kullar, HS ;
Watts, GDJ ;
Robinson, PJ ;
Taylor, AMR .
HUMAN MOLECULAR GENETICS, 1996, 5 (11) :1785-1791
[7]  
Chenevix-Trench G, 2002, JNCI-J NATL CANCER I, V94, P205, DOI 10.1093/jnci/94.3.205
[8]   CANCER RISKS IN A-T HETEROZYGOTES [J].
EASTON, DF .
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 1994, 66 (06) :S177-S182
[9]  
Esteller M, 2001, CANCER RES, V61, P3225
[10]  
Fang ZM, 2001, PATHOLOGY, V33, P30