Department of Cancer Prevention and Control, Roswell Park Comprehensive Cancer Center, Buffalo, NY, USA.
Division of Research, Kaiser Permanente Northern California, Oakland, CA, USA.
Mol Nutr Food Res. 2024 Apr;68(8):e2400087. doi: 10.1002/mnfr.202400087. Epub 2024 Apr 6.
Dietary isothiocyanate (ITC) exposure from cruciferous vegetable (CV) intake may improve non-muscle invasive bladder cancer (NMIBC) prognosis. This study aims to investigate whether genetic variations in key ITC-metabolizing/functioning genes modify the associations between dietary ITC exposure and NMIBC prognosis outcomes.
In the Bladder Cancer Epidemiology, Wellness, and Lifestyle Study (Be-Well Study), a prospective cohort of 1472 incident NMIBC patients, dietary ITC exposure is assessed by self-reported CV intake and measured in plasma ITC-albumin adducts. Using Cox proportional hazards regression models, stratified by single nucleotide polymorphisms (SNPs) in nine key ITC-metabolizing/functioning genes, it is calculate hazard ratios (HRs) and 95% confidence intervals (CIs) for recurrence and progression. The rs15561 in N-acetyltransferase 1 (NAT1) is alter the association between CV intake and progression risk. Multiple SNPs in nuclear factor E2-related factor 2 (NRF2) and nuclear factor kappa B (NFκB) are modify the associations between plasma ITC-albumin adduct level and progression risk (p < 0.05). No significant association is observed with recurrence risk. Overall, >80% study participants are present with at least one protective genotype per gene, showing an average 65% reduction in progression risk with high dietary ITC exposure.
Despite that genetic variations in ITC-metabolizing/functioning genes may modify the effect of dietary ITCs on NMIBC prognosis, dietary recommendation of CV consumption may help improve NMIBC survivorship.
十字花科蔬菜(CV)摄入的膳食异硫氰酸酯(ITC)暴露可能改善非肌肉浸润性膀胱癌(NMIBC)的预后。本研究旨在探讨关键 ITC 代谢/功能基因的遗传变异是否会改变膳食 ITC 暴露与 NMIBC 预后结果之间的关联。
在膀胱癌流行病学、健康和生活方式研究(Be-Well 研究)中,对 1472 名新发 NMIBC 患者进行了前瞻性队列研究,通过自我报告的 CV 摄入量和血浆 ITC-白蛋白加合物来评估膳食 ITC 暴露情况。使用 Cox 比例风险回归模型,按 9 个关键 ITC 代谢/功能基因中的单核苷酸多态性(SNP)进行分层,计算复发和进展的风险比(HRs)和 95%置信区间(CIs)。N-乙酰转移酶 1(NAT1)中的 rs15561 改变了 CV 摄入与进展风险之间的关联。核因子 E2 相关因子 2(NRF2)和核因子 kappa B(NFκB)中的多个 SNP 修饰了血浆 ITC-白蛋白加合物水平与进展风险之间的关联(p < 0.05)。与复发风险无显著关联。总体而言,> 80%的研究参与者在每个基因中至少存在一种保护性基因型,表明高膳食 ITC 暴露可使进展风险平均降低 65%。
尽管 ITC 代谢/功能基因中的遗传变异可能会改变膳食 ITC 对 NMIBC 预后的影响,但 CV 消费的膳食建议可能有助于改善 NMIBC 的生存。