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A Review: Epigenetic Mechanism in Ochratoxin A Toxicity Studies

Ochratoxin A (OTA) is a natural contaminant that has displayed nephrotoxicity and hepatotoxicity in mammals. It contaminates a great variety of foodstuffs and threatens people’s lives. The molecular mechanism of OTA-induced toxicity has been studied since 1965. Moreover, epigenetic mechanisms are al...

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Autores principales: Zhu, Liye, Zhang, Boyang, Dai, Yaqi, Li, Hongyu, Xu, Wentao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5408187/
https://www.ncbi.nlm.nih.gov/pubmed/28333080
http://dx.doi.org/10.3390/toxins9040113
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author Zhu, Liye
Zhang, Boyang
Dai, Yaqi
Li, Hongyu
Xu, Wentao
author_facet Zhu, Liye
Zhang, Boyang
Dai, Yaqi
Li, Hongyu
Xu, Wentao
author_sort Zhu, Liye
collection PubMed
description Ochratoxin A (OTA) is a natural contaminant that has displayed nephrotoxicity and hepatotoxicity in mammals. It contaminates a great variety of foodstuffs and threatens people’s lives. The molecular mechanism of OTA-induced toxicity has been studied since 1965. Moreover, epigenetic mechanisms are also studied in OTA-induced toxicity. Additionally, the mode of OTA epigenetic research has been advanced in research hotspots. However, there is still no epigenetic study of OTA-induced toxicity. In this review, we discuss the relationship between these epigenetic mechanisms and OTA-induced toxicity. We found that studies on the epigenetic mechanisms of OTA-induced toxicity all chose the whole kidney or liver as the model, which cannot reveal the real change in DNA methylation or miRNAs or histone in the target sites of OTA. Our recommendations are as follows: (1) the specific target site of OTA should be detected by advanced technologies; and (2) competing endogenous RNAs (ceRNA) should be explored with OTA.
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spelling pubmed-54081872017-05-03 A Review: Epigenetic Mechanism in Ochratoxin A Toxicity Studies Zhu, Liye Zhang, Boyang Dai, Yaqi Li, Hongyu Xu, Wentao Toxins (Basel) Review Ochratoxin A (OTA) is a natural contaminant that has displayed nephrotoxicity and hepatotoxicity in mammals. It contaminates a great variety of foodstuffs and threatens people’s lives. The molecular mechanism of OTA-induced toxicity has been studied since 1965. Moreover, epigenetic mechanisms are also studied in OTA-induced toxicity. Additionally, the mode of OTA epigenetic research has been advanced in research hotspots. However, there is still no epigenetic study of OTA-induced toxicity. In this review, we discuss the relationship between these epigenetic mechanisms and OTA-induced toxicity. We found that studies on the epigenetic mechanisms of OTA-induced toxicity all chose the whole kidney or liver as the model, which cannot reveal the real change in DNA methylation or miRNAs or histone in the target sites of OTA. Our recommendations are as follows: (1) the specific target site of OTA should be detected by advanced technologies; and (2) competing endogenous RNAs (ceRNA) should be explored with OTA. MDPI 2017-03-23 /pmc/articles/PMC5408187/ /pubmed/28333080 http://dx.doi.org/10.3390/toxins9040113 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Zhu, Liye
Zhang, Boyang
Dai, Yaqi
Li, Hongyu
Xu, Wentao
A Review: Epigenetic Mechanism in Ochratoxin A Toxicity Studies
title A Review: Epigenetic Mechanism in Ochratoxin A Toxicity Studies
title_full A Review: Epigenetic Mechanism in Ochratoxin A Toxicity Studies
title_fullStr A Review: Epigenetic Mechanism in Ochratoxin A Toxicity Studies
title_full_unstemmed A Review: Epigenetic Mechanism in Ochratoxin A Toxicity Studies
title_short A Review: Epigenetic Mechanism in Ochratoxin A Toxicity Studies
title_sort review: epigenetic mechanism in ochratoxin a toxicity studies
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5408187/
https://www.ncbi.nlm.nih.gov/pubmed/28333080
http://dx.doi.org/10.3390/toxins9040113
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