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Evidence of exposure to aristolochic acid in patients with urothelial cancer from a Balkan endemic nephropathy region of Romania
Authors:Heinz H Schmeiser  Jill E Kucab  Volker M Arlt  David H Phillips  Monica Hollstein  Gheorghe Gluhovschi  Cristina Gluhovschi  Mirela Modilca  Liviu Daminescu  Ligia Petrica  Silvia Velciov
Institution:1. Research Group Genetic Alterations in Carcinogenesis, German Cancer Research Center (DKFZ), Heidelberg, Germany;2. Analytical and Environmental Sciences Division, MRC‐HPA Centre for Environment & Health, King's College London, London, United Kingdom;3. Division of Genetics and Epidemiology, Institute of Cancer Research, Sutton, Surrey, United Kingdom;4. Faculty of Medicine and Health University of Leeds, Leeds, United Kingdom;5. Romanian Academy of Medical Sciences, Bucharest, Romania;6. Nephrology Department, University of Medicine and Pharmacy, Timisoara, Romania;7. Dialysis Center Renamed, Drobeta Turnu Severin, Romania;8. Urology Department, Emergency County Hospital Timisoara, Timisoara, Romania
Abstract:Recently, chronic Aristolochia poisoning was found responsible for the aetiology of Balkan endemic nephropathy (BEN) in Croatia, Serbia, and Bosnia, and diet was the likely route of exposure to aristolochic acid (AA). BEN, often associated with an increased incidence of upper urinary tract carcinoma (UUC), also affects residents of certain rural villages in Romania. AA is a nephrotoxin and human carcinogen that forms DNA adducts after metabolic activation, which induce characteristic TP53 mutations in urothelial tumours. Here we present the first evidence linking AA exposure to UUC in residents of an endemic region in the Romanian Mehedinti County. DNA was extracted from kidney and tumour tissue of seven patients who underwent nephroureterectomy for UUC and resided in BEN villages (endemic group). Five patients with UUC from nonendemic villages served as controls. AA‐DNA adducts (7‐(deoxyadenosin‐N6‐yl)‐aristolactam I), established biomarkers of AA exposure, were identified by 32P‐postlabelling in renal DNA of six patients from the endemic group and in one of the nonendemic group (adduct levels ranged from 0.3 to 6.5 adducts per 108 nucleotides). Additionally, an A to T transversion in TP53, a base substitution characteristic of AA mutagenic activity was found in urothelial tumour DNA of one patient from the endemic group. Our results provide a molecular link to the cause of urothelial tumours in BEN regions of Romania indicating that AA is the common aetiological agent for BEN across its numerous geographical foci. Environ. Mol. Mutagen., 2012. © 2012 Wiley Periodicals, Inc.
Keywords:aristolochic acid  Balkan endemic nephropathy  urothelial cancer  DNA adduct
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