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Analyses of biomarkers of exposure to nephrotoxic mycotoxins in a cohort of patients with renal tumours
F. Malir, M. Louda, V. Ostry, J. Toman, N. Ali, Y. Grosse, E. Malirova, J. Pacovsky, D. Pickova, M. Brodak, A. Pfohl-Leszkowicz, GH. Degen,
Jazyk angličtina Země Německo
Typ dokumentu časopisecké články
Grantová podpora
2118/2015
University Hradec Kralove, Czech Republic
2113/2016
University Hradec Kralove, Czech Republic
2105/2017
University Hradec Kralove, Czech Republic
NIPH, IN 75010330
Ministry of Health, Czech Republic conceptual development of research organization
- MeSH
- biologické markery krev moč MeSH
- chromatografie kapalinová MeSH
- citrinin krev moč MeSH
- dospělí MeSH
- kohortové studie MeSH
- lidé středního věku MeSH
- lidé MeSH
- mykotoxiny krev moč MeSH
- nádory ledvin chemie moč MeSH
- ochratoxiny krev moč MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- tandemová hmotnostní spektrometrie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Geografické názvy
- Československo MeSH
The Czech Republic occupies the first place in the world in the frequency of renal and other urinary tract tumours, but their aetiology is unknown. To explore whether carcinogenic and nephrotoxic mycotoxins may contribute to kidney diseases in the Czech population, biomarkers of ochratoxin A (OTA) and citrinin (CIT) exposure were determined in biological specimens from a cohort of 50 patients with malignant renal tumours. Biomarker analyses in blood and urine samples used validated targeted methods for measuring OTA and CIT plus dihydrocitrinone (DH-CIT) after enrichment of analytes by specific immunoaffinity clean-up. OTA and CIT plus its metabolite DH-CIT were frequently detected in patient urine samples (OTA 62%; CIT 91%; DH-CIT 100%). The concentration ranges in urine were 1-27.8 ng/L for OTA, 2-87 ng/L for CIT and 2-160 ng/L for DH-CIT. The analyses of blood samples revealed also a frequent co-occurrence of OTA and CIT, in the ranges of 40-870 ng/L serum for OTA and 21-182 ng/L plasma for CIT. This first analysis of biomarkers in blood and urine samples of Czech patients revealed no major differences in comparison with published data for the general healthy Czech and European populations. Nonetheless, a frequent co-occurrence of CIT and OTA biomarkers in patient samples may be of interest with regard to potential interactions with other risk factors for renal disease.
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- $a 10.1007/s12550-019-00365-9 $2 doi
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- $a Malir, Frantisek $u Department of Biology, Faculty of Science, University of Hradec Králové, Rokitanskeho 62,, 500 03, Hradec Kralove, Czech Republic. frantisek.malir@uhk.cz.
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- $a Analyses of biomarkers of exposure to nephrotoxic mycotoxins in a cohort of patients with renal tumours / $c F. Malir, M. Louda, V. Ostry, J. Toman, N. Ali, Y. Grosse, E. Malirova, J. Pacovsky, D. Pickova, M. Brodak, A. Pfohl-Leszkowicz, GH. Degen,
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- $a The Czech Republic occupies the first place in the world in the frequency of renal and other urinary tract tumours, but their aetiology is unknown. To explore whether carcinogenic and nephrotoxic mycotoxins may contribute to kidney diseases in the Czech population, biomarkers of ochratoxin A (OTA) and citrinin (CIT) exposure were determined in biological specimens from a cohort of 50 patients with malignant renal tumours. Biomarker analyses in blood and urine samples used validated targeted methods for measuring OTA and CIT plus dihydrocitrinone (DH-CIT) after enrichment of analytes by specific immunoaffinity clean-up. OTA and CIT plus its metabolite DH-CIT were frequently detected in patient urine samples (OTA 62%; CIT 91%; DH-CIT 100%). The concentration ranges in urine were 1-27.8 ng/L for OTA, 2-87 ng/L for CIT and 2-160 ng/L for DH-CIT. The analyses of blood samples revealed also a frequent co-occurrence of OTA and CIT, in the ranges of 40-870 ng/L serum for OTA and 21-182 ng/L plasma for CIT. This first analysis of biomarkers in blood and urine samples of Czech patients revealed no major differences in comparison with published data for the general healthy Czech and European populations. Nonetheless, a frequent co-occurrence of CIT and OTA biomarkers in patient samples may be of interest with regard to potential interactions with other risk factors for renal disease.
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- $a Louda, Miroslav $u Medical School and Teaching Hospital, Department of Urology, Charles University, Sokolska 581,, 500 05, Hradec Kralove, Czech Republic.
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- $a Ostry, Vladimir $u Department of Biology, Faculty of Science, University of Hradec Králové, Rokitanskeho 62,, 500 03, Hradec Kralove, Czech Republic. Center for Health, Nutrition and Food in Brno, National Institute of Public Health in Prague, Palackeho 3a, 612 42, Brno, Czech Republic.
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- $a Toman, Jakub $u Department of Biology, Faculty of Science, University of Hradec Králové, Rokitanskeho 62,, 500 03, Hradec Kralove, Czech Republic.
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- $a Ali, Nurshad $u Department of Biochemistry and Molecular Biology, Shahjalal University of Science and Technology, Sylhet, 3114, Bangladesh.
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- $a Grosse, Yann $u International Agency for Research on Cancer, 150 Cours Albert Thomas, 69372, Lyon Cedex 08, France.
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- $a Malirova, Eva $u Department of Clinical Biochemistry, Charles University Medical School and Teaching Hospital, Sokolska 581, 50005, Hradec Kralove, Czech Republic.
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- $a Pacovsky, Jaroslav $u Medical School and Teaching Hospital, Department of Urology, Charles University, Sokolska 581,, 500 05, Hradec Kralove, Czech Republic.
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- $a Pickova, Darina $u Department of Biology, Faculty of Science, University of Hradec Králové, Rokitanskeho 62,, 500 03, Hradec Kralove, Czech Republic.
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- $a Brodak, Milos $u Medical School and Teaching Hospital, Department of Urology, Charles University, Sokolska 581,, 500 05, Hradec Kralove, Czech Republic.
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- $a Pfohl-Leszkowicz, Annie $u INP/ENSAT Toulouse, Department Bioprocess & Microbial Systems, Laboratory Chemical Engineering, University of Toulouse, 31320, Auzeville-Tolosane, France.
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- $a Degen, Gisela H $u Leibniz Research Centre for Working Environment and Human Factors (IfADo), Ardeystrasse 67, 44139, Dortmund, Germany.
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- $w MED00192822 $t Mycotoxin research $x 1867-1632 $g Roč. 35, č. 4 (2019), s. 391-403
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