In situ analyses of genome instability in breast cancer

被引:290
作者
Chin, K
de Solorzano, CO
Knowles, D
Jones, A
Chou, W
Rodriguez, EG
Kuo, WL
Ljung, BM
Chew, K
Myambo, K
Miranda, M
Krig, S
Garbe, J
Stampfer, M
Yaswen, P
Gray, JW [1 ]
Lockett, SJ
机构
[1] Univ Calif San Francisco, Dept Lab Med, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Ctr Comprehens Canc, San Francisco, CA 94143 USA
[3] Univ Calif Berkeley, Lawrence Berkeley Lab, Div Life Sci, Berkeley, CA 94720 USA
[4] Univ Calif Berkeley, Lawrence Berkeley Lab, Div Engn, Berkeley, CA 94720 USA
[5] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/ng1409
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Transition through telomere crisis is thought to be a crucial event in the development of most breast carcinomas. Our goal in this study was to determine where this occurs in the context of histologically defined breast cancer progression. To this end, we assessed genome instability (using fluorescence in situ hybridization) and other features associated with telomere crisis in normal ductal epithelium, usual ductal hyperplasia, ductal carcinoma in situ and invasive cancer. We modeled this process in vitro by measuring these same features in human mammary epithelial cell cultures during ZNF217-mediated transition through telomere crisis and immortalization. Taken together, the data suggest that transition through telomere crisis and immortalization in breast cancer occurs during progression from usual ductal hyperplasia to ductal carcinoma in situ.
引用
收藏
页码:984 / 988
页数:5
相关论文
共 31 条
[11]   Telomerase: biology and phase I trials [J].
Kelland, Lloyd R. .
LANCET ONCOLOGY, 2001, 2 (02) :95-102
[12]   A low threshold level of expression of mutant-template telomerase RNA inhibits human tumor cell proliferation [J].
Kim, MM ;
Rivera, MA ;
Botchkina, IL ;
Shalaby, R ;
Thor, AD ;
Blackburn, EH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (14) :7982-7987
[13]   Online access to CGH data of DNA sequence copy number changes [J].
Knuutila, S ;
Autio, K ;
Aalto, Y .
AMERICAN JOURNAL OF PATHOLOGY, 2000, 157 (02) :689-689
[14]  
Kuukasjarvi T, 1997, CANCER RES, V57, P1597
[15]  
Kuukasjarvi T, 1997, AM J PATHOL, V150, P1465
[16]   Connecting chromosomes, crisis, and cancer [J].
Maser, RS ;
DePinho, RA .
SCIENCE, 2002, 297 (5581) :565-569
[17]   Telomere shortening occurs in subsets of normal breast epithelium as well as in situ and invasive carcinoma [J].
Meeker, AK ;
Hicks, JL ;
Gabrielson, E ;
Strauss, WM ;
De Marzo, AM ;
Argani, P .
AMERICAN JOURNAL OF PATHOLOGY, 2004, 164 (03) :925-935
[18]  
Nishizaki T, 1997, GENE CHROMOSOME CANC, V19, P267, DOI 10.1002/(SICI)1098-2264(199708)19:4<267::AID-GCC9>3.0.CO
[19]  
2-V
[20]  
Nonet GH, 2001, CANCER RES, V61, P1250