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Arsenic Exposure and Cancer-Related Proteins in Urine of Indigenous Bolivian Women

Indigenous people living in the Bolivian Andes are exposed through their drinking water to inorganic arsenic, a potent carcinogen. However, the health consequences of arsenic exposure in this region are unknown. The aim of this study was to evaluate associations between arsenic exposure and changes...

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Autores principales: De Loma, Jessica, Gliga, Anda R., Levi, Michael, Ascui, Franz, Gardon, Jacques, Tirado, Noemi, Broberg, Karin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7767847/
https://www.ncbi.nlm.nih.gov/pubmed/33381488
http://dx.doi.org/10.3389/fpubh.2020.605123
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author De Loma, Jessica
Gliga, Anda R.
Levi, Michael
Ascui, Franz
Gardon, Jacques
Tirado, Noemi
Broberg, Karin
author_facet De Loma, Jessica
Gliga, Anda R.
Levi, Michael
Ascui, Franz
Gardon, Jacques
Tirado, Noemi
Broberg, Karin
author_sort De Loma, Jessica
collection PubMed
description Indigenous people living in the Bolivian Andes are exposed through their drinking water to inorganic arsenic, a potent carcinogen. However, the health consequences of arsenic exposure in this region are unknown. The aim of this study was to evaluate associations between arsenic exposure and changes in cancer-related proteins in indigenous women (n = 176) from communities around the Andean Lake Poopó, Bolivia. Arsenic exposure was assessed in whole blood (B-As) and urine (as the sum of arsenic metabolites, U-As) by inductively coupled plasma-mass spectrometry (ICP-MS). Cancer-related proteins (N = 92) were measured in urine using the proximity extension assay. The median B-As concentration was 2.1 (range 0.60–9.1) ng/g, and U-As concentration was 67 (12–399) μg/L. Using linear regression models adjusted for age, urinary osmolality, and urinary leukocytes, we identified associations between B-As and four putative cancer-related proteins: FASLG, SEZ6L, LYPD3, and TFPI2. Increasing B-As concentrations were associated with lower protein expression of SEZ6L, LYPD3, and TFPI2, and with higher expression of FASLG in urine (no association was statistically significant after correcting for multiple comparisons). The associations were similar across groups with different arsenic metabolism efficiency, a susceptibility factor for arsenic toxicity. In conclusion, arsenic exposure in this region was associated with changes in the expression of some cancer-related proteins in urine. Future research is warranted to understand if these proteins could serve as valid biomarkers for arsenic-related toxicity.
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spelling pubmed-77678472020-12-29 Arsenic Exposure and Cancer-Related Proteins in Urine of Indigenous Bolivian Women De Loma, Jessica Gliga, Anda R. Levi, Michael Ascui, Franz Gardon, Jacques Tirado, Noemi Broberg, Karin Front Public Health Public Health Indigenous people living in the Bolivian Andes are exposed through their drinking water to inorganic arsenic, a potent carcinogen. However, the health consequences of arsenic exposure in this region are unknown. The aim of this study was to evaluate associations between arsenic exposure and changes in cancer-related proteins in indigenous women (n = 176) from communities around the Andean Lake Poopó, Bolivia. Arsenic exposure was assessed in whole blood (B-As) and urine (as the sum of arsenic metabolites, U-As) by inductively coupled plasma-mass spectrometry (ICP-MS). Cancer-related proteins (N = 92) were measured in urine using the proximity extension assay. The median B-As concentration was 2.1 (range 0.60–9.1) ng/g, and U-As concentration was 67 (12–399) μg/L. Using linear regression models adjusted for age, urinary osmolality, and urinary leukocytes, we identified associations between B-As and four putative cancer-related proteins: FASLG, SEZ6L, LYPD3, and TFPI2. Increasing B-As concentrations were associated with lower protein expression of SEZ6L, LYPD3, and TFPI2, and with higher expression of FASLG in urine (no association was statistically significant after correcting for multiple comparisons). The associations were similar across groups with different arsenic metabolism efficiency, a susceptibility factor for arsenic toxicity. In conclusion, arsenic exposure in this region was associated with changes in the expression of some cancer-related proteins in urine. Future research is warranted to understand if these proteins could serve as valid biomarkers for arsenic-related toxicity. Frontiers Media S.A. 2020-12-14 /pmc/articles/PMC7767847/ /pubmed/33381488 http://dx.doi.org/10.3389/fpubh.2020.605123 Text en Copyright © 2020 De Loma, Gliga, Levi, Ascui, Gardon, Tirado and Broberg. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Public Health
De Loma, Jessica
Gliga, Anda R.
Levi, Michael
Ascui, Franz
Gardon, Jacques
Tirado, Noemi
Broberg, Karin
Arsenic Exposure and Cancer-Related Proteins in Urine of Indigenous Bolivian Women
title Arsenic Exposure and Cancer-Related Proteins in Urine of Indigenous Bolivian Women
title_full Arsenic Exposure and Cancer-Related Proteins in Urine of Indigenous Bolivian Women
title_fullStr Arsenic Exposure and Cancer-Related Proteins in Urine of Indigenous Bolivian Women
title_full_unstemmed Arsenic Exposure and Cancer-Related Proteins in Urine of Indigenous Bolivian Women
title_short Arsenic Exposure and Cancer-Related Proteins in Urine of Indigenous Bolivian Women
title_sort arsenic exposure and cancer-related proteins in urine of indigenous bolivian women
topic Public Health
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7767847/
https://www.ncbi.nlm.nih.gov/pubmed/33381488
http://dx.doi.org/10.3389/fpubh.2020.605123
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