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Endocrine-Related Cancer 12 (4) 945-952    DOI: 10.1677/erc.1.01083
Copyright © 2005 by the Society for Endocrinology.
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Increased risk of ovarian cancer in integrin ß3 Leu33Pro homozygotes

S E Bojesen1, S K Kjær2, E V S Høgdall2, B L Thomsen2, C K Høgdall3, J Blaakær2, A Tybjærg-Hansen4,5 and B G Nordestgaard1,4

1 Department of Clinical Biochemistry, Herlev University Hospital, Herlev Ringvej 75, DK-2730 Herlev, Denmark
2 Institute of Cancer Epidemiology, Danish Cancer Society, Strandboulevarden 49, DK-2100 Copenhagen Ø, Denmark
3 Gynaecologic Clinic, Rigshospitalet, Copenhagen University Hospital, Blegdamsvej 9, DK-2100 Copenhagen Ø, Denmark
4 The Copenhagen City Heart Study, Bispebjerg University Hospital, Bispebjerg Bakke 23, DK-2400 Copenhagen NV, Denmark
5 Department of Clinical Biochemistry, Rigshospitalet, Copenhagen University Hospital, Blegdamsvej 9, DK-2100 Copenhagen Ø, Denmark

(Requests for offprints should be addressed to B G Nordestgaard, Department of Clinical Biochemistry, Herlev University Hospital, Herlev Ringvej 75, DK-2730 Herlev, Denmark. Email: brno{at}herlevhosp.kbhamt.dk)

We previously demonstrated that integrin ß3 Leu33Pro homozygotes have an increased risk of cancer, possibly most pronounced for ovarian cancer. We now test the latter hypothesis in case-control and prospective studies. We genotyped 463 Danish women with ovarian cancer, and 4291 women from the Danish general population. Calculation of odds ratios by conditional logistic regression was performed in the case-control study (n=463 + 3543), and of ovarian cancer incidence, log-rank statistics and hazard ratios by Cox regression in the prospective study (n=4291) with 9.5-year follow-up. In the case-control study matched for age and marital status, the odds ratio for ovarian cancer in homozygotes versus non-carriers was 1.6 (95% confidence interval: 1.0–2.6). In the prospective study with 28 incident ovarian cancers, non-carriers and homozygotes had incidences of 7 (4–11) and 30 (10–92) per 10 000 person-years (log-rank P=0.02). The age-adjusted hazard ratio for ovarian cancer in homozygotes versus non-carriers was 3.9 (1.1–13). Risk of ovarian cancer did not differ between heterozygotes and non-carriers in either study. Integrin ß3 Leu33Pro homozygotes have an increased risk of ovarian cancer.




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A. Jakubowska, J. Gronwald, J. Menkiszak, B. Gorski, T. Huzarski, T. Byrski, L. Edler, J. Lubinski, R. J Scott, and U. Hamann
Integrin {beta}3 Leu33Pro polymorphism increases BRCA1-associated ovarian cancer risk
J. Med. Genet., June 1, 2007; 44(6): 408 - 411.
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