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A multidisciplinary approach disclosing unexplored Aflatoxin B1 roles in severe impairment of vitamin D mechanisms of action
Aflatoxin B1 (AFB1), produced by fungi of the genus Aspergillus, is the most toxic and carcinogenic mycotoxin among the classes of aflatoxins. Previous research showed that AFB1 affects vitamin D receptor (VDR) expression. In the present study, integrated computational and experimental studies were...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Netherlands
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10425525/ https://www.ncbi.nlm.nih.gov/pubmed/36066700 http://dx.doi.org/10.1007/s10565-022-09752-y |
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author | Persico, Marco Sessa, Raffaele Cesaro, Elena Dini, Irene Costanzo, Paola Ritieni, Alberto Fattorusso, Caterina Grosso, Michela |
author_facet | Persico, Marco Sessa, Raffaele Cesaro, Elena Dini, Irene Costanzo, Paola Ritieni, Alberto Fattorusso, Caterina Grosso, Michela |
author_sort | Persico, Marco |
collection | PubMed |
description | Aflatoxin B1 (AFB1), produced by fungi of the genus Aspergillus, is the most toxic and carcinogenic mycotoxin among the classes of aflatoxins. Previous research showed that AFB1 affects vitamin D receptor (VDR) expression. In the present study, integrated computational and experimental studies were carried out to investigate how AFB1 can interfere with Vitamin D signalling. A competitive antagonism of AFB1 toward RXRα and VDR was hypothesized by comparing the docked complex of AFB1/RXRα and AFB1/VDR ligand-binding domain (LBD) with the X-ray structures of RXRα and VDR bound to known ligands. Accordingly, we demonstrated that AFB1 can affect vitamin D-mediated transcriptional activation of VDR by impairing the formation of protein complexes containing both VDR-RXRα and RXRα/RAR and affecting the subcellular localization of VDR and RXRα. As a whole, our data indicate that AFB1 can interfere with different molecular pathways triggered by vitamin D with an antagonistic mechanism of action. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10565-022-09752-y. |
format | Online Article Text |
id | pubmed-10425525 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-104255252023-08-16 A multidisciplinary approach disclosing unexplored Aflatoxin B1 roles in severe impairment of vitamin D mechanisms of action Persico, Marco Sessa, Raffaele Cesaro, Elena Dini, Irene Costanzo, Paola Ritieni, Alberto Fattorusso, Caterina Grosso, Michela Cell Biol Toxicol Original Article Aflatoxin B1 (AFB1), produced by fungi of the genus Aspergillus, is the most toxic and carcinogenic mycotoxin among the classes of aflatoxins. Previous research showed that AFB1 affects vitamin D receptor (VDR) expression. In the present study, integrated computational and experimental studies were carried out to investigate how AFB1 can interfere with Vitamin D signalling. A competitive antagonism of AFB1 toward RXRα and VDR was hypothesized by comparing the docked complex of AFB1/RXRα and AFB1/VDR ligand-binding domain (LBD) with the X-ray structures of RXRα and VDR bound to known ligands. Accordingly, we demonstrated that AFB1 can affect vitamin D-mediated transcriptional activation of VDR by impairing the formation of protein complexes containing both VDR-RXRα and RXRα/RAR and affecting the subcellular localization of VDR and RXRα. As a whole, our data indicate that AFB1 can interfere with different molecular pathways triggered by vitamin D with an antagonistic mechanism of action. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10565-022-09752-y. Springer Netherlands 2022-09-06 2023 /pmc/articles/PMC10425525/ /pubmed/36066700 http://dx.doi.org/10.1007/s10565-022-09752-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Persico, Marco Sessa, Raffaele Cesaro, Elena Dini, Irene Costanzo, Paola Ritieni, Alberto Fattorusso, Caterina Grosso, Michela A multidisciplinary approach disclosing unexplored Aflatoxin B1 roles in severe impairment of vitamin D mechanisms of action |
title | A multidisciplinary approach disclosing unexplored Aflatoxin B1 roles in severe impairment of vitamin D mechanisms of action |
title_full | A multidisciplinary approach disclosing unexplored Aflatoxin B1 roles in severe impairment of vitamin D mechanisms of action |
title_fullStr | A multidisciplinary approach disclosing unexplored Aflatoxin B1 roles in severe impairment of vitamin D mechanisms of action |
title_full_unstemmed | A multidisciplinary approach disclosing unexplored Aflatoxin B1 roles in severe impairment of vitamin D mechanisms of action |
title_short | A multidisciplinary approach disclosing unexplored Aflatoxin B1 roles in severe impairment of vitamin D mechanisms of action |
title_sort | multidisciplinary approach disclosing unexplored aflatoxin b1 roles in severe impairment of vitamin d mechanisms of action |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10425525/ https://www.ncbi.nlm.nih.gov/pubmed/36066700 http://dx.doi.org/10.1007/s10565-022-09752-y |
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