Epidemiology and Community Health Branch, National Heart Lung and Blood Institute, National Institutes of Health, Bethesda, Maryland, USA.
Occupational and Environmental Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, Maryland, USA.
Environ Mol Mutagen. 2024 Jan-Feb;65(1-2):47-54. doi: 10.1002/em.22588. Epub 2024 Mar 11.
The etiology of bladder cancer among never smokers without occupational or environmental exposure to established urothelial carcinogens remains unclear. Urinary mutagenicity is an integrative measure that reflects recent exposure to genotoxic agents. Here, we investigated its potential association with bladder cancer in rural northern New England. We analyzed 156 bladder cancer cases and 247 cancer-free controls from a large population-based case-control study conducted in Maine, New Hampshire, and Vermont. Overnight urine samples were deconjugated enzymatically and the extracted organics were assessed for mutagenicity using the plate-incorporation Ames assay with the Salmonella frameshift strain YG1041 + S9. Logistic regression was used to estimate the odds ratios (OR) and 95% confidence intervals (CI) of bladder cancer in relation to having mutagenic versus nonmutagenic urine, adjusted for age, sex, and state, and stratified by smoking status (never, former, and current). We found evidence for an association between having mutagenic urine and increased bladder cancer risk among never smokers (OR = 3.8, 95% CI: 1.3-11.2) but not among former or current smokers. Risk could not be estimated among current smokers because nearly all cases and controls had mutagenic urine. Urinary mutagenicity among never-smoking controls could not be explained by recent exposure to established occupational and environmental mutagenic bladder carcinogens evaluated in our study. Our findings suggest that among never smokers, urinary mutagenicity potentially reflects genotoxic exposure profiles relevant to bladder carcinogenesis. Future studies are needed to replicate our findings and identify compounds and their sources that influence bladder cancer risk.
在没有职业或环境暴露于已确定的尿路上皮致癌剂的情况下,从不吸烟的膀胱癌的病因仍不清楚。尿液致突变性是一种综合指标,反映了最近接触遗传毒性剂的情况。在这里,我们研究了其与新英格兰北部农村地区膀胱癌的潜在关联。我们分析了缅因州、新罕布什尔州和佛蒙特州进行的一项大型基于人群的病例对照研究中的 156 例膀胱癌病例和 247 例无癌症对照。将过夜尿液样品进行酶去共轭,并使用沙门氏菌移码菌株 YG1041+S9 的平板掺入 Ames 测定法评估提取的有机物的致突变性。使用逻辑回归估计与具有致突变性尿液而非非致突变性尿液相关的膀胱癌的优势比(OR)和 95%置信区间(CI),并根据年龄、性别和州进行调整,并按吸烟状况(从不吸烟、曾经吸烟和当前吸烟)分层。我们发现,具有致突变性尿液与从不吸烟者膀胱癌风险增加之间存在关联(OR=3.8,95%CI:1.3-11.2),但与曾经吸烟者或当前吸烟者无关。由于几乎所有病例和对照都具有致突变性尿液,因此无法对当前吸烟者进行风险估计。在从不吸烟的对照中,尿液致突变性不能用我们研究中评估的最近接触已确定的职业性和环境性致突变膀胱癌致癌物来解释。我们的研究结果表明,在从不吸烟者中,尿液致突变性可能反映了与膀胱癌发生有关的遗传毒性暴露情况。需要进一步的研究来复制我们的发现并确定影响膀胱癌风险的化合物及其来源。