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Title: Comparative genomic hybridization reveals many new loci containing amplified genes in breast cancer

Conference · · Cytometry (Baltimore); (United States)
OSTI ID:6558362
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  1. Univ. of California, San Francisco (United States) GBCRI, San Francisco, CA (United States) MRC Genetics Unit, Edinburgh (United Kingdom)

The authors have developed a powerful new technique, comparative genomic hybridization (CGH), for molecular cytogenetic analysis of solid tumors. In CGH, differentially labeled total tumor DNA and normal reference DNA are allowed to compete for their binding sites in a normal metaphase spread. After immunofluorescent staining, the relative copy numbers of all regions in the tumor genome can be quantitiated with an image analysis system by measuring the intensity ratios of the two fluorochromes along the length of each chromosome. They used CGH to study gene amplification and other chromosomal changes in 16 breast cancer cell lines and 20 primary tumors. The loci undergoing amplification were highly variable from one sample to another and over 20 distinct sites were identified. Some sites correspond to locations of known oncogenes (e.g. erbb2 at 17q12 and myc at 8q24) whereas most of them (e.g. 6p22, 11p15, 17q22) are not previously known to contain amplified oncogenes. Frequent changes affecting larger chromosomal regions, such as duplications of 1q and deletions of 1p32-35, have also been found. CGH can dramatically facilitate identification of commonly altered chromosomal loci in cancer.

DOE Contract Number:
AC03-76SF00098
OSTI ID:
6558362
Report Number(s):
CONF-9303114-; CODEN: CYTODQ; CNN: CA 45919; CA 47537
Journal Information:
Cytometry (Baltimore); (United States), Vol. 6; Conference: 16. congress of the International Society for Analytical Cytology, Colorado Springs, CO (United States), 21-26 Mar 1993; ISSN 0196-4763
Country of Publication:
United States
Language:
English