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Cancer Epidemiology Biomarkers & Prevention Vol. 13, 438-444, March 2004
© 2004 American Association for Cancer Research

Insulin-Like Growth Factor (IGF)-1, IGF-Binding Protein-3, and Pancreatic Cancer in Male Smokers

Rachael Z. Stolzenberg-Solomon1, Paul Limburg2, Michael Pollak3, Philip R. Taylor4, Jarmo Virtamo5 and Demetrius Albanes1

1 Nutritional Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD; 2 Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN; 3 Cancer Prevention Program, Jewish General Hospital and McGill University, Montreal, Canada; 4 Cancer Prevention Studies Branch, Division of Clinical Sciences, National Cancer Institute, Bethesda, MD; and 5 Department of Epidemiology and Health Promotion, National Public Health Institute, Helsinki, Finland

Requests for reprints: Rachel Stolzenberg-Solomon, NCI, NIH, Nutritional Epidemiology, 6120 Executive Boulevard, Suite 320, (EPS) Room 7039, MSC 7232, Bethesda, MD 20892-7232. Phone: (301) 594-2939; Fax: (301) 496-6829. E-mail: rs221z{at}nih.gov

To investigate whether insulin-like growth factor (IGF)-1 and IGF-binding protein-3 (IGFBP-3) are prospectively associated with exocrine pancreatic cancer, we conducted a nested case-control study within the Alpha-Tocopherol, Beta-Carotene Cancer Prevention Study cohort of 29,133 male Finnish smokers, aged 50–69 years. To avoid the potential influence of subclinical cancer on IGF-1 and IGFBP-3, all subjects in this study were alive without clinical evidence of cancer during their 5th year of the cohort follow-up. Four hundred randomly selected cohort controls and 93 incident pancreatic adenocarcinoma cases that occurred between their 5th follow-up year through 1997 (i.e., up to 12.7 years of follow-up) were included in this study. Concentrations of IGF-1 and IGFBP-3 were measured in serum samples obtained at baseline using ELISA. Odds ratios (ORs) and 95% confidence intervals (CIs) were estimated using logistic regression models, adjusted for confounders. Neither IGF-1, IGFBP-3, nor the IGF-1:IGFBP-3 molar ratio was significantly associated with pancreatic cancer: highest compared to lowest tertile, OR = 0.67, 95% CI 0.37–1.21, P trend = 0.17; OR = 0.70, 95% CI 0.38–1.27, P trend = 0.12; and OR = 0.85, 95% CI 0.50–1.46, P trend = 0.54, respectively. Our results do not support the hypothesis that serum IGF-1 and IGFBP-3 concentrations are associated with pancreatic cancer risk among male smokers. Further studies are necessary to evaluate these associations in other populations.




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Molecular Cancer Research Cancer Prevention Research
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Copyright © 2004 by the American Association for Cancer Research.