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Comparative genomic hybridization analysis on male breast cancer
Author(s) -
Rudlowski Christian,
Schulten HansJürgen,
Golas Mariola Monika,
Sander Bjoern,
Barwing Roland,
Palandt JensEkkehard,
Schlehe Bettina,
Lindenfelser Rüdiger,
Moll Roland,
Liersch Torsten,
Schumpelick Volker,
Gunawan Bastian,
Füzesi László
Publication year - 2006
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/ijc.21646
Subject(s) - comparative genomic hybridization , breast cancer , malignancy , biology , cancer , cytogenetics , oncology , medicine , pathology , cancer research , genetics , chromosome , gene
The spectrum of genetic alterations in primary male breast cancer is not well established. We analyzed chromosomal imbalances in 39 tumor samples from primary male breast cancer by comparative genomic hybridization (CGH) and correlated CGH findings with clinicopathological factors. Chromosomal gains were most frequent at 1q (46%), 8q (46%), 16p (36%), 17q (36%), Xq (28%), 20q (26%) and Xp (18%). Losses were most commonly observed at 8p (36%), 16q (28%), 13q (28%), 6q (18%), 11q (18%) and 22q (18%). Gains at 16p, 20q and Xq and losses at 13q correlated significantly with higher degree of cytogenetic complexity. Significant associations with clinicopathological factors were observed for +8q and −16q with larger tumor size and −16q with lower proliferative activity and lower grade of malignancy. A comparison with reported CGH data from female breast cancer showed a similar pattern of chromosomal imbalances, including +1q, −8p, +8q, −13q, +16p, −16q, +17q and +20q. Our results indicate that male breast cancer shares a common pattern of imbalances with female breast cancer, suggesting that similar genetic events may underlie the development and progression of male and female breast cancer. © 2005 Wiley‐Liss, Inc.