Molecular characterization of the t(3;9) associated with immortalization in the MCF10A cell line

被引:55
作者
Cowell, JK [1 ]
LaDuca, J [1 ]
Rossi, MR [1 ]
Burkhardt, T [1 ]
Nowak, NJ [1 ]
Matsui, S [1 ]
机构
[1] Roswell Pk Canc Inst, Dept Canc Genet, Buffalo, NY 14263 USA
关键词
D O I
10.1016/j.cancergencyto.2005.04.019
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The t(3;9)(p14;p21) in the MCF10A human mammary gland epithelial cell line was the single cytogenetic event that accompanied the transition from primary culture to immortalized cell line, suggesting that it is related to the development of the immortalization phenotype. To study the molecular consequences of the breakpoints in this rearrangement, we used a combination of fluorescence in situ hybridization (FISH) and array comparative genomic hybridization (CGH). The 3p14 translocation breakpoint occurs within BAC RP11-795e22, which accommodates only the TA-FA1 gene, a novel cysteine-rich secreted protein thought to be involved in cytokine signaling. TA-FA1 is expressed in normal breast tissue, not in MCF10A, and shows differential expression in a range of breast cancer cell lines. The 9p translocation breakpoint results in a deletion of approximately 4 megabases on the derivative chromosome 9, which includes the CDKN2A (p,16) gene. Array CGH and FISH analysis demonstrated that BAC 149i22, which contains the CDKN2A/B genes, is also deleted specifically on the apparently normal copy of chromosome 9, making MCF10A null for the p16/p15 genes. The exact extent of gains and losses of chromosome regions resulting from rearrangements involving chromosomes 1q, 5q, and 8q have also been characterized using the BAC arrays. (c) 2005 Elsevier Inc. All rights reserved.
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页码:23 / 29
页数:7
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