Affiliations of authors: Department of Nutrition (KZ, MJS, EG), Department of Epidemiology (LM, MJS, EG), and Department of Biostatistics (BAR), Harvard School of Public Health, Boston, MA; Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA (LM, BAR, MJS, EG); Department of Internal Medicine, The Ohio State University, Columbus, OH (SKC); Department of Pathology, Dana-Farber Cancer Institute, Boston, MA (ML).
J Natl Cancer Inst. 2014 Feb;106(2):djt430. doi: 10.1093/jnci/djt430. Epub 2014 Jan 24.
The role of lycopene in prostate cancer prevention remains controversial. We examined the associations between dietary lycopene intake and prostate cancer, paying particular attention to the influence of prostate-specific antigen screening, and evaluated tissue biomarkers in prostate cancers in relation to lycopene intake.
Among 49898 male health professionals, we obtained dietary information through questionnaires and ascertained total and lethal prostate cancer cases from 1986 through January 31, 2010. Cox regression was used to estimate multivariable hazard ratios (HRs) and 95% confidence intervals (CIs). Tissue microarrays and immunohistochemistry were used to assess tumor biomarker expression in a subset of men. Two-sided χ(2) tests were used to calculate the P values.
Higher lycopene intake was inversely associated with total prostate cancer and more strongly with lethal prostate cancer (top vs bottom quintile: HR = 0.72; 95% CI = 0.56 to 0.94; P(trend) = .04). In a restricted population of screened participants, the inverse associations became markedly stronger (for lethal prostate cancer: HR = 0.47; 95% CI = 0.29 to 0.75; P trend = .009). Comparing different measures of dietary lycopene, early intake, but not recent intake, was inversely associated with prostate cancer. Higher lycopene intake was associated with biomarkers in the cancer indicative of less angiogenic potential.
Dietary intake of lycopene was associated with reduced risk of lethal prostate cancer and with a lesser degree of angiogenesis in the tumor. Because angiogenesis is a strong progression factor, an endpoint of lethal prostate cancer may be more relevant than an endpoint of indolent prostate cancer for lycopene in the era of highly prevalent prostate-specific antigen screening.
番茄红素在前列腺癌预防中的作用仍存在争议。我们研究了膳食番茄红素摄入量与前列腺癌之间的关联,特别关注前列腺特异性抗原筛查的影响,并评估了与番茄红素摄入量相关的前列腺癌组织生物标志物。
在 49898 名男性健康专业人员中,我们通过问卷调查获得了饮食信息,并从 1986 年至 2010 年 1 月 31 日确定了总前列腺癌和致命性前列腺癌病例。使用 Cox 回归估计多变量风险比(HR)和 95%置信区间(CI)。使用组织微阵列和免疫组织化学技术评估了一部分男性的肿瘤生物标志物表达。使用双侧 χ(2)检验计算 P 值。
较高的番茄红素摄入量与总前列腺癌呈负相关,与致命性前列腺癌的相关性更强(最高五分位与最低五分位相比:HR=0.72;95%CI=0.56 至 0.94;P 趋势=0.04)。在经过筛选的参与者的受限人群中,这种负相关变得更为明显(致命性前列腺癌:HR=0.47;95%CI=0.29 至 0.75;P 趋势=0.009)。比较不同的膳食番茄红素测量方法,早期摄入量而非近期摄入量与前列腺癌呈负相关。较高的番茄红素摄入量与癌症标志物相关,表明其血管生成潜力较低。
饮食中番茄红素的摄入与致命性前列腺癌风险降低以及肿瘤中血管生成程度降低有关。由于血管生成是一个强烈的进展因素,在前列腺特异性抗原筛查广泛普及的时代,致死性前列腺癌的终点可能比惰性前列腺癌的终点与番茄红素更相关。