Gene expression profiles of epithelial cells microscopically isolated from a breast-invasive ductal carcinoma and a nodal metastasis

被引:89
作者
Zucchi, I
Mento, E
Kuznetsov, VA
Scotti, M
Valsecchi, V
Simionati, B
Vicinanza, E
Valle, G
Pilotti, S
Reinbold, R
Vezzoni, P
Albertini, A
Dulbecco, R
机构
[1] CNR, Ist Tecnol Biomed, Milan, Italy
[2] Genome Inst Singapore, Dept Informat & Math Sci, Singapore 138672, Singapore
[3] Univ Padua, Ctr Ric Interdipartimentale Biotecnol Innovat, I-35121 Padua, Italy
[4] Ist Nazl Tumori, I-20133 Milan, Italy
[5] Max Planck Inst Mol Biomed Cell & Dev Biol, D-48149 Munster, Germany
[6] Salk Inst Biol Studies, La Jolla, CA 92037 USA
关键词
breast cancer; serial analysis of gene expression; cell microdissection; carcinoma;
D O I
10.1073/pnas.0408260101
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Expression profiles of breast carcinomas are difficult to interpret when they are obtained from tissue in toto, which may contain a large proportion of non-cancer cells. To avoid this problem, we microscopically isolated cells from a primary invasive ductal carcinoma of the breast and from an axillary node harboring a metastatic breast carcinoma, to obtain pure populations of carcinoma cells (approximate to500) and used them for serial analysis of gene expression. The expression profiles generated from both populations of cells were compared with the profile of a disease-free mammary epithelium. We showed that the expression profiles obtained are exclusive of carcinoma cells with no contribution of non-epithelial cells. From a total of 16,939 unique tags analyzed, we detected 559 statistically significant changes in gene expression; some of these genes have not been previously associated with breast cancer. We observed that many of the down-regulated genes are the same in both cancers, whereas the up-regulated genes are completely different, suggesting that the down-regulation of a set of genes may be the basic mechanism of cancer formation, while the up-regulation may characterize and possibly control the state of evolution of individual cancers. The results obtained may help in characterizing the neoplastic process of breast cancer.
引用
收藏
页码:18147 / 18152
页数:6
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