Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland, USA.
Cancer Research Technology Program, Leidos Biomedical Research, Inc., Frederick National Laboratory for Cancer Research, Frederick, Maryland, USA.
Cancer Rep (Hoboken). 2022 Jul;5(7):e1574. doi: 10.1002/cnr2.1574. Epub 2021 Nov 11.
The overall incidence of gastric cancer in women is half that in men for most global populations. Sex hormone pathways may be involved in carcinogenesis and estrogens have been postulated to protect women against gastric cancer.
To evaluate associations of gastric cancer with estrogen metabolites in postmenopausal women.
We performed an analysis of 233 gastric cancer cases and 281 age-matched controls from three prospective cohorts and two case-control studies of early-stage gastric cancer, mainly conducted in high-risk Asian populations. Fifteen estrogen-parent (estrone and estradiol) and -metabolite analytes (2-hydroxyestrone, 2-hydroxyestradiol, 2-hydroxyestrone-3-methyl ether, 4-hydroxyestrone; 4-methoxyestrone, 4-methoxyestradiol, 2-methoxyestrone, 2-methoxyestradiol, estriol, 16α-hydroxyestrone, 16-ketoestradiol, 16-epiestriol, and 17-epiestriol) were measured in spot urines using liquid chromatography-tandem mass spectrometry. Odds ratios for association with each marker were estimated by logistic regression. Heterogeneity was assessed by Cochran's Q test. Study-specific odds ratios were pooled by fixed-effects meta-analysis. Urinary levels of estrogen-related molecules were not associated with gastric cancer (adjusted odds ratios ranged from 0.87 to 1.27; p-values >.05), with low between-study heterogeneity (p-values >.1) for all but two metabolites (2-hydroxyestrone-3-methyl ether and 2-methoxyestradiol).
To date, this is the first comprehensive assessment of endogenous estrogens with gastric cancer risk in women. Estrogens do not appear to have an etiologic role in gastric cancer risk among postmenopausal women. Given the complex network of sex steroid hormones and their extreme variation over the lifespan, further evaluation of this hypothesis is warranted.
在大多数全球人群中,女性胃癌的总体发病率是男性的一半。性激素途径可能参与了致癌作用,并且雌激素被认为可以保护女性免受胃癌的侵害。
评估绝经后妇女中胃癌与雌激素代谢物的相关性。
我们对三个前瞻性队列和两个早期胃癌病例对照研究中的 233 例胃癌病例和 281 例年龄匹配的对照进行了分析,这些研究主要在高危亚洲人群中进行。使用液相色谱-串联质谱法在点尿中测定了 15 种雌激素母体(雌酮和雌二醇)和 -代谢物分析物(2-羟基雌酮、2-羟基雌二醇、2-羟基雌酮-3-甲醚、4-羟基雌酮;4-甲氧基雌酮、4-甲氧基雌二醇、2-甲氧基雌酮、2-甲氧基雌二醇、雌三醇、16α-羟基雌酮、16-酮雌二醇、16-表雌三醇和 17-表雌三醇)。使用逻辑回归估计每个标志物与关联的比值比。通过 Cochran's Q 检验评估异质性。通过固定效应荟萃分析对研究特异性比值比进行汇总。雌激素相关分子的尿液水平与胃癌无关(调整后的比值比范围为 0.87 至 1.27;p 值>.05),除两种代谢物(2-羟基雌酮-3-甲醚和 2-甲氧基雌二醇)外,所有代谢物的研究间异质性均较低(p 值>.1)。
迄今为止,这是首次对绝经后妇女体内雌激素与胃癌风险进行的全面评估。雌激素似乎在绝经后妇女的胃癌风险中没有病因作用。鉴于甾体激素的复杂网络及其在整个生命周期中的极端变化,进一步评估这一假设是有必要的。