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Koul A, Malander S, Loman N, et al. BRCA1 and BRCA2 mutations in ovarian cancer: Covariation with specific cytogenetic features. Int J Gynecol Cancer. 2000;10(4):289-295doi: 10.1046/j.1525-1438.2000.010004289.x.
Koul, A., Malander, S., Loman, N., Pejovic, T., Heim, S., Willen, R., Johannsson, O., Olsson, H., Ridderheim, M., & Borg Å. (2000). BRCA1 and BRCA2 mutations in ovarian cancer: Covariation with specific cytogenetic features. International journal of gynecological cancer : official journal of the International Gynecological Cancer Society, 10(4), 289-295. https://doi.org/10.1046/j.1525-1438.2000.010004289.x
Koul, A., et al. "BRCA1 and BRCA2 mutations in ovarian cancer: Covariation with specific cytogenetic features." International journal of gynecological cancer : official journal of the International Gynecological Cancer Society vol. 10,4 (2000): 289-295. doi: https://doi.org/10.1046/j.1525-1438.2000.010004289.x
Koul A, Malander S, Loman N, Pejovic T, Heim S, Willen R, Johannsson O, Olsson H, Ridderheim M, Borg Å. BRCA1 and BRCA2 mutations in ovarian cancer: Covariation with specific cytogenetic features. Int J Gynecol Cancer. 2000 Jul;10(4):289-295. doi: 10.1046/j.1525-1438.2000.010004289.x. PMID: 11240689.
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Int J Gynecol Cancer. 2000 Jul;10(4):289-295. doi: 10.1046/j.1525-1438.2000.010004289.x.

BRCA1 and BRCA2 mutations in ovarian cancer: Covariation with specific cytogenetic features.

International journal of gynecological cancer : official journal of the International Gynecological Cancer Society

A. Koul, S. Malander, N. Loman, T. Pejovic, S. Heim, R. Willen, O. Johannsson, H. Olsson, M. Ridderheim, Å. Borg Å

Affiliations

  1. Departments of Oncology, Gynecological Oncology and Pathology, University Hospital, S-221 85, Lund, Sweden;Yale Hospital of New Haven, Connecticut; and Department of Genetics, The Norwegian Radium Hospital and Institute for Cancer Research, Oslo, Norway.

PMID: 11240689 DOI: 10.1046/j.1525-1438.2000.010004289.x

Abstract

We analyzed 37 primary invasive carcinomas for BRCA1 and BRCA2 mutations by screening the entire coding regions of both genes. Seven predicted truncating mutations (four in BRCA1 and three in BRCA2) and one novel BRCA1 missense variant (S1542C) were identified (8/37, 22%). Two of the BRCA1 mutations were somatic changes, whereas the remaining three BRCA1 changes and all mutations of BRCA2 were found to be of germline origin. All eight BRCA-positive tumors were serous or seropapillary carcinomas (8/27 serous tumors, 30%), and all but one were poorly differentiated. The correlation between tumor karyotype and BRCA status showed that clonal chromosomal aberrations were present in all BRCA-positive tumors (8/8) compared with 20 of 29 BRCA-negative ones. The most consistently affected region in BRCA-positive tumors was the long arm of chromosome 6; alterations within this arm with a breakpoint in band 6q21 were seen in four of five BRCA1-positive and in two of three BRCA2-positive tumors, but only in four of 20 karyotypically abnormal tumors without BRCA mutations, suggesting that the genetic pathways of tumor progression differ in the two groups. The high frequency of germline BRCA mutations detected in this pilot study (16% of 37 invasive carcinomas) points to the need for more extended analyses of population-based series of patients to determine the true contribution of these predisposing genes to the overall incidence of ovarian cancer in this population.

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