Literature DB >> 12237896

Circulating levels of insulin-like growth factor-I and risk of ovarian cancer.

Annekatrin Lukanova1, Eva Lundin, Paolo Toniolo, Andrea Micheli, Arslan Akhmedkhanov, Sabina Rinaldi, Paola Muti, Per Lenner, Carine Biessy, Vittorio Krogh, Anne Zeleniuch-Jacquotte, Franco Berrino, Göran Hallmans, Elio Riboli, Rudolf Kaaks.   

Abstract

Insulin-like growth factor (IGF)-I, a mitogenic and anti-apoptotic peptide, has been implicated in the development of several cancers. We hypothesized that high circulating IGF-I concentrations may be associated with an increased risk of ovarian cancer. A case-control study was nested within 3 prospective cohorts in New York (USA), Umeå (Sweden) and Milan (Italy). One hundred thirty-two women with primary invasive epithelial ovarian cancer diagnosed at least 1 year after blood donation were case subjects. For each case, 2 control subjects were selected, matching the case subject on cohort, menopausal status, age and date of recruitment (n = 263). Only women who did not use exogenous hormones at blood donation were included in the study. There was no association between IGF-I concentrations and ovarian cancer risk in the study group as a whole. In analyses restricted to subjects who had developed ovarian cancer at a young age (<55), circulating IGF-I was directly and strongly associated with ovarian cancer risk (OR = 4.97; 95% CI = 1.22-20.2 for the top vs. the bottom IGF-I tertile after adjustment for parity, BMI categories and smoking). There was no significant association of IGF binding protein-3 with ovarian cancer risk. We found a strong direct relationship between circulating IGF-I levels and risk of developing ovarian cancer before age 55. Additional, larger studies of this association are needed to provide more precise estimates of effect. Copyright 2002 Wiley-Liss, Inc.

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Year:  2002        PMID: 12237896     DOI: 10.1002/ijc.10613

Source DB:  PubMed          Journal:  Int J Cancer        ISSN: 0020-7136            Impact factor:   7.396


  44 in total

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