Screening breast cancer patients for ATM mutations and polymorphisms by using denaturing high-performance liquid chromatography

被引:22
作者
Atencio, DP
Iannuzzi, CM
Green, S
Stock, RG
Bernstein, JL
Rosenstein, BS
机构
[1] Mt Sinai Sch Med, Dept Radiat Oncol, New York, NY 10029 USA
[2] Mt Sinai Sch Med, Dept Community & Prevent Med, New York, NY 10029 USA
[3] Mt Sinai Sch Med, Dept Dermatol, New York, NY 10029 USA
[4] NYU, Sch Med, Dept Radiat Oncol, New York, NY USA
关键词
African American; ATM; breast cancer; DHPLC; mutations; polymorphisms;
D O I
10.1002/em.1072
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
All 62 coding exons of the ATM gene, along with 10-20 bases of the intronic region flanking each exon, were screened for DNA base sequence alterations by using denaturing high-performance liquid chromatography (DHPLC) in a series of 52 breast cancer patients. Six (12%) of these patients exhibited a total of eight different novel germ-line mutations that do not represent common polymorphisms. Of these, three patients possessed four nonconservative missense mutations while two conservative missense and two synonymous mutations were detected in the other three patients. In addition, 43 patients were found to have a total of 141 DNA sequence variations representing 21 different common polymorphisms and rare variants. An analysis of the relationship between the presence of a novel ATM mutation and either patient demographics or tumor properties demonstrated a significant difference between African Americans (3/ 7 = 43%) and other ethnic groups (3/45 = 7%, P = 0.026). None of the other characteristics examined was found to be related to mutation status. (C) 2001 Wiley-Liss, Inc.
引用
收藏
页码:200 / 208
页数:9
相关论文
共 96 条
[1]  
Arnold N, 1999, HUM MUTAT, V14, P333, DOI 10.1002/(SICI)1098-1004(199910)14:4<333::AID-HUMU9>3.3.CO
[2]  
2-3
[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]   Enhanced phosphorylation of p53 by ATN in response to DNA damage [J].
Banin, S ;
Moyal, L ;
Shieh, SY ;
Taya, Y ;
Anderson, CW ;
Chessa, L ;
Smorodinsky, NI ;
Prives, C ;
Reiss, Y ;
Shiloh, Y ;
Ziv, Y .
SCIENCE, 1998, 281 (5383) :1674-1677
[5]  
Bay JO, 1998, INT J ONCOL, V12, P1385
[6]  
Bénit P, 2000, HUM MUTAT, V16, P417
[7]   ATM-heterozygous germline mutations contribute to breast cancer-susceptibility [J].
Broeks, A ;
Urbanus, JHM ;
Floore, AN ;
Dahler, EC ;
Klijn, JGM ;
Rutgers, EJT ;
Devilee, P ;
Russell, NS ;
van Leeuwen, FE ;
van't Veer, LJ .
AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 66 (02) :494-500
[8]   Direct inhibition of the signaling functions of the mammalian target of rapamycin by the phosphoinositide 3-kinase inhibitors, wortmannin and LY294002 [J].
Brunn, GJ ;
Williams, J ;
Sabers, C ;
Wiederrecht, G ;
Lawrence, JC ;
Abraham, RT .
EMBO JOURNAL, 1996, 15 (19) :5256-5267
[9]   Activation of the ATM kinase by ionizing radiation and phosphorylation of p53 [J].
Canman, CE ;
Lim, DS ;
Cimprich, KA ;
Taya, Y ;
Tamai, K ;
Sakaguchi, K ;
Appella, E ;
Kastan, MB ;
Siliciano, JD .
SCIENCE, 1998, 281 (5383) :1677-1679
[10]  
Castellví-Bel S, 1999, HUM MUTAT, V14, P156, DOI 10.1002/(SICI)1098-1004(1999)14:2<156::AID-HUMU7>3.0.CO