Woodson Karen, Tangrea Joseph A, Pollak Michael, Copeland Terry D, Taylor Philip R, Virtamo Jarmo, Albanes Demetrius
Cancer Prevention Studies Branch, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland 20892, USA.
Cancer Res. 2003 Jul 15;63(14):3991-4.
Recent epidemiological studies suggest an association between higher blood levels of insulin-like growth factor I (IGF-I) and increased risk of prostate cancer. We evaluated the association between prediagnostic levels of IGF-I and insulin-like growth factor binding protein 3 (IGFBP-3) and prostate cancer risk in a nested case-control study within the Alpha-Tocopherol, Beta-Carotene Cancer Prevention Study. Within the same cohort (using different cases and controls who had sequential serum samples available) we also examined changes in serum IGF-I and IGFBP-3 levels over time by case status. The risk association study included incident prostate cancer cases (n = 100) diagnosed at least 5 years after baseline blood draw (range, 5-12 years; median 9 years) and frequency-matched (4:1) controls. The sequential serum study included all of the prostate cancer cases (n = 21) with prediagnostic (2-3 years before diagnosis) and diagnostic serum available, and pair-matched controls (1:1). An ELISA was used to quantitate serum levels of IGF-I and IGFBP-3 for both studies. The association between IGF-I or IGFBP-3 and prostate cancer risk was assessed using conditional logistic regression, and paired t tests were used to evaluate case-control differences in change in serum analytes over time. We found no significant association between either IGF-I or IGFBP-3 and prostate cancer risk. In a multivariate analysis, we observed an odds ratio of 0.52 (95% confidence interval, 0.23-1.16) for the fourth versus the first quartile of serum IGF-I. Serum IGF-I, but not IGFBP-3, increased significantly over time in cases (18% increase) but not controls (4% decrease; P = 0.02). In contrast to previous reports, we found no evidence to support a causal association between serum IGF-I or IGFBP-3 and the risk of prostate cancer. It is possible that serum IGF-I may be serving as a tumor marker rather than an etiologic factor in prostate cancer.
近期的流行病学研究表明,血液中胰岛素样生长因子I(IGF-I)水平升高与前列腺癌风险增加之间存在关联。在α-生育酚、β-胡萝卜素癌症预防研究的巢式病例对照研究中,我们评估了诊断前IGF-I和胰岛素样生长因子结合蛋白3(IGFBP-3)水平与前列腺癌风险之间的关联。在同一队列中(使用有连续血清样本的不同病例和对照),我们还按病例状态检查了血清IGF-I和IGFBP-3水平随时间的变化。风险关联研究纳入了在基线采血至少5年后(范围为5 - 12年;中位数为9年)诊断出的前列腺癌新发病例(n = 100)以及频率匹配(4:1)的对照。连续血清研究纳入了所有有诊断前(诊断前2 - 3年)和诊断时血清样本的前列腺癌病例(n = 21)以及配对对照(1:1)。两项研究均使用酶联免疫吸附测定法(ELISA)定量血清IGF-I和IGFBP-3水平。使用条件逻辑回归评估IGF-I或IGFBP-3与前列腺癌风险之间的关联,并使用配对t检验评估血清分析物随时间变化的病例对照差异。我们发现IGF-I或IGFBP-3与前列腺癌风险之间均无显著关联。在多变量分析中,我们观察到血清IGF-I第四四分位数与第一四分位数相比的比值比为0.52(95%置信区间,0.23 - 1.16)。病例组血清IGF-I随时间显著升高(升高18%),而对照组则下降(下降4%;P = 0.02),IGFBP-3则不然。与先前的报告相反,我们没有发现证据支持血清IGF-I或IGFBP-3与前列腺癌风险之间存在因果关联。血清IGF-I有可能是前列腺癌的肿瘤标志物而非病因学因素。