Black Amanda, Pinsky Paul F, Grubb Robert L, Falk Roni T, Hsing Ann W, Chu Lisa, Meyer Tamra, Veenstra Timothy D, Xu Xia, Yu Kai, Ziegler Regina G, Brinton Louise A, Hoover Robert N, Cook Michael B
Divisions of Cancer Epidemiology and Genetics and
Cancer Prevention, National Cancer Institute, NIH, DHHS, Rockville, Maryland.
Cancer Epidemiol Biomarkers Prev. 2014 Nov;23(11):2374-82. doi: 10.1158/1055-9965.EPI-14-0700. Epub 2014 Sep 1.
The combined action of androgens and estrogens-specifically their balance-may play a role in prostate carcinogenesis, but existing evidence is sparse and inconsistent. We investigated associations between serum sex steroid hormones, including estrogen metabolites, and risk of aggressive prostate cancer.
In a case-control study nested within the Prostate, Lung, Colorectal and Ovarian Cancer Screening Trial cohort, we measured serum estrone, estradiol, and 13 estrogen metabolites, in the 2-, 4-, or 16-hydroxylation pathways, using an LC/MS-MS assay. Cases (n = 195) were non-Hispanic white men ages 55 to 70 years when diagnosed with aggressive prostate cancer (stage III or IV and/or Gleason ≥7). Controls (n = 195) were non-Hispanic white men without prostate cancer who were frequency matched to cases by age and year at blood draw, and time since baseline screen. Only men with serum testosterone and sex hormone-binding globulin measured previously were eligible. Logistic regression models were used to estimate ORs and 95% confidence intervals (95% CI).
Risk of aggressive prostate cancer was strongly inversely associated with estradiol:testosterone ratio (OR4th quartile vs. 1st = 0.27; 95% CI, 0.12-0.59, Ptrend = 0.003) and positively associated with 2:16α-hydroxyestrone ratio (OR4th quartile vs. 1st = 2.44; 95% CI, 1.34-4.45, Ptrend = 0.001). Individual estrogen metabolites were unrelated to risk.
Our findings suggest that sex steroid hormones, specifically the estrogen-androgen balance, may be important in the development of aggressive prostate cancer.
Improved understanding of the hormonal etiology of prostate cancer is critical for prevention and therapeutic interventions.
雄激素和雌激素的联合作用——尤其是它们之间的平衡——可能在前列腺癌发生过程中起作用,但现有证据稀少且不一致。我们研究了包括雌激素代谢物在内的血清性激素与侵袭性前列腺癌风险之间的关联。
在一项嵌套于前列腺、肺、结肠直肠和卵巢癌筛查试验队列中的病例对照研究中,我们使用液相色谱/串联质谱分析法测量了2-、4-或16-羟基化途径中的血清雌酮、雌二醇和13种雌激素代谢物。病例(n = 195)为确诊患有侵袭性前列腺癌(III期或IV期和/或Gleason评分≥7)的55至70岁非西班牙裔白人男性。对照(n = 195)为无前列腺癌的非西班牙裔白人男性,按年龄、采血年份和自基线筛查以来的时间与病例进行频率匹配。仅先前测量过血清睾酮和性激素结合球蛋白的男性符合条件。使用逻辑回归模型估计比值比(OR)和95%置信区间(95%CI)。
侵袭性前列腺癌风险与雌二醇:睾酮比值呈强烈负相关(第四四分位数与第一四分位数相比,OR = 0.27;95%CI,0.12 - 0.59,P趋势 = 0.003),与2:16α-羟基雌酮比值呈正相关(第四四分位数与第一四分位数相比,OR = 2.44;95%CI,1.34 - 4.45,P趋势 = 0.001)。个体雌激素代谢物与风险无关。
我们的研究结果表明,性激素,特别是雌激素 - 雄激素平衡,可能在侵袭性前列腺癌的发生发展中起重要作用。
更好地理解前列腺癌的激素病因对于预防和治疗干预至关重要。