Additive Effects of Arsenic and Aristolochic Acid in Chemical Carcinogenesis of Upper Urinary Tract Urothelium

被引:14
作者
Chen, Chung-Hsin [1 ]
Grollman, Arthur P. [2 ,3 ]
Huang, Chao-Yuan [1 ]
Shun, Chia-Tung [4 ]
Sidorenko, Viktoriya S. [2 ]
Hashimoto, Keiji [2 ]
Moriya, Masaaki [2 ]
Turesky, Robert J. [5 ,6 ]
Yun, Byeong Hwa [5 ,6 ]
Tsai, Karen [7 ]
Wu, Stephanie [7 ]
Chuang, Po-Ya [8 ]
Tang, Chao-Hsiun [8 ]
Yang, Wen-Horng [9 ]
Tzai, Tzong-Shin [9 ]
Tsai, Yuh-Shyan [9 ]
Dickman, Kathleen G. [2 ,3 ]
Pu, Yeong-Shiau [1 ]
机构
[1] Natl Taiwan Univ Hosp, Dept Urol, Taipei, Taiwan
[2] SUNY Stony Brook, Dept Pharmacol Sci, Stony Brook, NY 11794 USA
[3] SUNY Stony Brook, Dept Med, Stony Brook, NY 11794 USA
[4] Natl Taiwan Univ Hosp, Dept Forens Med & Pathol, Taipei, Taiwan
[5] Univ Minnesota, Masonic Canc Ctr, Minneapolis, MN USA
[6] Univ Minnesota, Dept Med Chem, Minneapolis, MN 55455 USA
[7] SUNY Stony Brook, Sch Med, Stony Brook, NY 11794 USA
[8] Taipei Med Univ, Sch Hlth Care Adm, Taipei, Taiwan
[9] Natl Cheng Kung Univ, Natl Cheng Kung Univ Hosp, Dept Urol, Coll Med, Tainan, Taiwan
关键词
BLADDER-CANCER; DNA ADDUCTS; CARCINOMA; TISSUES; PERFORMANCE; EXPOSURE; RISK;
D O I
10.1158/1055-9965.EPI-20-1090
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Aristolochic acids (AA) and arsenic are chemical carcinogens associated with urothelial carcinogenesis. Here we investigate the combined effects of AA and arsenic toward the risk of developing upper tract urothelial carcinoma (UTUC). Methods: Hospital-based (n = 89) and population-based (2,921 cases and 11,684 controls) Taiwanese UTUC cohorts were used to investigate the association between exposure to AA and/or arsenic and the risk of developing UTUC. In the hospital cohort, AA exposure was evaluated by measuring aristolactam-DNA adducts in the renal cortex and by identifying A>T TP53 mutations in tumors. In the population cohort, AA exposure was determined from prescription health insurance records. Arsenic levels were graded from 0 to 3 based on concentrations in well water and the presence of arseniasis-related diseases. Results: In the hospital cohort, 43, 26, and 20 patients resided in grade 0, 1+2, and 3 arseniasis-endemic areas, respectively. Aristolactam-DNA adducts were present in >90% of these patients, indicating widespread AA exposure. A>T mutations in TP53 were detected in 28%, 44%, and 22% of patients residing in grade 0, 1+2, and 3 arseniasis-endemic areas, respectively. Population studies revealed that individuals who consumed more AA-containing herbs had a higher risk of developing UTUC in both arseniasis-endemic and nonendemic areas. Logistic regression showed an additive effect of AA and arsenic exposure on the risk of developing UTUC. Conclusions: Exposure to both AA and arsenic acts additively to increase the UTUC risk in Taiwan. Impact: This is the first study to investigate the combined effect of AA and arsenic exposure on UTUC.
引用
收藏
页码:317 / 325
页数:9
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