High-resolution representational oligonucleotide microarray analysis and fluorescence in situ hybridization analysis of aneuploid and diploid breast tumors
Year: 2005
Type: article
Study design: Observational Study
Abstract: Combining representational oligonucleotide microarray analysis (ROMA) of tumor DNA with quantitative multigene fluorescence in situ hybridization (QM-FISH) of individual tumor cells provides the opportunity to detect and validate a wide range of gene amplifications, deletions, duplications and rearrangements directly in frozen tumor samples. We have used these combined techniques to examine 101 aneuploid and diploid breast tumors (highly aneuploid A-tumors and pseudo-diploid D-tumors), for which long-term follow-up and detailed clinical information were available. We have determined that ROMA provides accurate and sensitive detection of duplications, amplifications and deletions, and it yields defined boundaries for these events with a resolution of less than 50 kbp in most cases. Diploid tumors are particularly useful subjects for this approach, revealing complex rearrangements and repeated sequential amplification events on certain chromosomes that provide unique insights into the genomic progression of the disease. First, the fine structure of these amplification clusters, as detected by ROMA and quantitatively validated by FISH, provides extremely high-resolution 'pointers' to potential novel oncogenes, since many of the detected amplicons contain only one or two known or prospective genes. Second, FISH patterns provide a means for interpretation of the mechanism of these events. Third, the reproducibility and frequency of these events, especially in very early stage tumors, provides insight into the earliest chromosomal events in breast cancer. Finally, we have identified correlations between certain sets of rearrangement events and clinically relevant parameters such as long-term survival. These correlations may enable novel and powerful prognostic indicators for breast cancer and other cancers when more samples can be examined.
Source: Breast Cancer Research
DOI: 10.1186/bcr1069
Authors: J Hicks, V Grubor, N Navin, P Lundin, S Månér, T Hägerström, L Skoog, M Wigler, A Zetterberg
Institutions: Cold Spring Harbor Laboratory, Karolinska Institutet
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $4,190
Funders: U.S. Department of Defense, U.S. Department of Health and Human Services, Morris Animal Foundation, Florida State University, Kræftens Bekæmpelse, Kreftforeningen, Cancer Research UK, Breast Cancer Campaign, Macquarie University, Deutsche Forschungsgemeinschaft, Ministerstvo Zdravotnictví Ceské Republiky, Fondation de France, KWF Kankerbestrijding, Associazione Italiana per la Ricerca sul Cancro, Universitetet i Oslo, Norges Forskningsråd, Vedecká Grantová Agentúra MŠVVaŠ SR a SAV, Regione Marche, National Institutes of Health, Instituto de Salud Carlos III, National Cancer Institute
OpenAlex ID: W1518923136