Genetic alteration of chromosome 8 is a common feature of human mammary epithelial cell lines transformed in vitro with benzo[a]pyrene

被引:19
作者
Caruso, JA
Reiners, JJ
Émond, J
Shultz, T
Tainsky, MA
Alaoui-Jamali, M
Batist, G
机构
[1] Sir Mortimer B Davis Jewish Hosp, Lady Davis Inst Med Res, McGill Ctr Translat Res Canc, Montreal, PQ H3T 1E2, Canada
[2] Wayne State Univ, Inst Chem Toxicol, Detroit, MI 48201 USA
[3] Montreal Gen Hosp, Dept Pathol, Montreal, PQ H3G 1A4, Canada
[4] Wayne State Univ, Barbara Ann Karmanos Canc Inst, Detroit, MI USA
关键词
breast cancer; MCF-10A; benzo[a]pyrene; human chromosome 8; c-Myc; spectral karyotyping;
D O I
10.1016/S0027-5107(00)00140-8
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
While some epidemiological risk factors for breast cancer have been identified, the environmental factors responsible for transformation of mammary epithelial cells are not clear. We have exposed the spontaneously immortalized human mammary epithelial cell line MCF-10A to benzo[a]pyrene and selected transformed clones based on a loss of contact inhibition and anchorage-dependent growth. Cytogenetic studies showed that each of the transformed sublines possess an isochromosome 8q aberration. The c-Myc proto-oncogene, which is positioned at 8q24, was analyzed fur changes in expression. Both c-Myc mRNA and protein levels were increased in the transformed clones relative to the parental cells. The transformed clones were not able to grow as tumors in vivo when injected into nude or SCID mice. To determine whether the involvement of chromosome 8 in BP-induced mutagenesis was a reproducible event, transformed clones were selected from three additional independently treated sets of BP-exposed MCF-10A cultures and analyzed by spectral karyotyping (SKY). These transformed sublines also harbored the isochromosome 8q abnormality. Data from this model show that benzo[a]pyrene, a ubiquitous procarcinogen. can induce selectable morphologic changes in a human mammary epithelial cell line, and that these transformed cells possess chromosomal aberrations frequently found in human breast tumors, (C) 2001 Elsevier Science B.V. All rights reserved.
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收藏
页码:85 / 99
页数:15
相关论文
共 67 条
[1]   Fluorescence in situ hybridization assessment of chromosome 8 copy number in stage I and stage II infiltrating ductal carcinoma of the breast [J].
Afify, A ;
Mark, HFL .
CANCER GENETICS AND CYTOGENETICS, 1997, 97 (02) :101-105
[2]   Fluorescent in situ hybridization assessment of chromosome 8 copy number in breast cancer [J].
Afify, A ;
Bland, KI ;
Mark, HFL .
BREAST CANCER RESEARCH AND TREATMENT, 1996, 38 (02) :201-208
[3]   ONCOGENE AMPLIFICATION AND PROGNOSIS IN BREAST-CANCER - RELATIONSHIP WITH SYSTEMIC TREATMENT [J].
BERNS, EMJJ ;
FOEKENS, JA ;
VANSTAVEREN, IL ;
VANPUTTEN, WLJ ;
DEKONING, HYWCM ;
PORTENGEN, H ;
KLIJN, JGM .
GENE, 1995, 159 (01) :11-18
[4]  
Berns EMJJ, 1996, GENE CHROMOSOME CANC, V16, P170, DOI 10.1002/(SICI)1098-2264(199607)16:3<170::AID-GCC3>3.3.CO
[5]  
2-B
[6]   PREVALENCE OF AMPLIFICATION OF THE ONCOGENES C-MYC, HER2 NEU, AND INT-2 IN 1000 HUMAN BREAST-TUMORS - CORRELATION WITH STEROID-RECEPTORS [J].
BERNS, EMJJ ;
KLIJN, JGM ;
VANSTAVEREN, IL ;
PORTENGEN, H ;
NOORDEGRAAF, E ;
FOEKENS, JA .
EUROPEAN JOURNAL OF CANCER, 1992, 28A (2-3) :697-700
[7]  
BRENNER AJ, 1995, CANCER RES, V55, P2892
[8]  
Buerger H, 1999, J PATHOL, V189, P521, DOI 10.1002/(SICI)1096-9896(199912)189:4<521::AID-PATH472>3.0.CO
[9]  
2-B
[10]  
Buerger H, 1999, J PATHOL, V187, P396, DOI 10.1002/(SICI)1096-9896(199903)187:4<396::AID-PATH286>3.0.CO