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Retinaldehyde Dehydrogenase Inhibition-Related Adverse Outcome Pathway: Potential Risk of Retinoic Acid Synthesis Inhibition during Embryogenesis

Retinoic acid (RA) is one of the factors crucial for cell growth, differentiation, and embryogenesis; it interacts with the retinoic acid receptor and retinoic acid X receptor to eventually regulate target gene expression in chordates. RA is transformed from retinaldehyde via oxidization by retinald...

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Autores principales: Cho, Kichul, Lee, Sang-Moo, Heo, Jina, Kwon, Yong Min, Chung, Dawoon, Yu, Woon-Jong, Bae, Seung Seob, Choi, Grace, Lee, Dae-Sung, Kim, Youngjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8623920/
https://www.ncbi.nlm.nih.gov/pubmed/34822523
http://dx.doi.org/10.3390/toxins13110739
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author Cho, Kichul
Lee, Sang-Moo
Heo, Jina
Kwon, Yong Min
Chung, Dawoon
Yu, Woon-Jong
Bae, Seung Seob
Choi, Grace
Lee, Dae-Sung
Kim, Youngjun
author_facet Cho, Kichul
Lee, Sang-Moo
Heo, Jina
Kwon, Yong Min
Chung, Dawoon
Yu, Woon-Jong
Bae, Seung Seob
Choi, Grace
Lee, Dae-Sung
Kim, Youngjun
author_sort Cho, Kichul
collection PubMed
description Retinoic acid (RA) is one of the factors crucial for cell growth, differentiation, and embryogenesis; it interacts with the retinoic acid receptor and retinoic acid X receptor to eventually regulate target gene expression in chordates. RA is transformed from retinaldehyde via oxidization by retinaldehyde dehydrogenase (RALDH), which belongs to the family of oxidoreductases. Several chemicals, including disulphiram, diethylaminobenzaldehyde, and SB-210661, can effectively inhibit RALDH activity, potentially causing reproductive and developmental toxicity. The modes of action can be sequentially explained based on the molecular initiating event toward key events, and finally the adverse outcomes. Adverse outcome pathway (AOP) is a conceptual and theoretical framework that describes the sequential chain of casually liked events at different biological levels from molecular events to adverse effects. In the present review, we discussed a recently registered AOP (AOP(297); inhibition of retinaldehyde dehydrogenase leads to population decline) to explain and support the weight of evidence for RALDH inhibition-related developmental toxicity using the existing knowledge.
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spelling pubmed-86239202021-11-27 Retinaldehyde Dehydrogenase Inhibition-Related Adverse Outcome Pathway: Potential Risk of Retinoic Acid Synthesis Inhibition during Embryogenesis Cho, Kichul Lee, Sang-Moo Heo, Jina Kwon, Yong Min Chung, Dawoon Yu, Woon-Jong Bae, Seung Seob Choi, Grace Lee, Dae-Sung Kim, Youngjun Toxins (Basel) Review Retinoic acid (RA) is one of the factors crucial for cell growth, differentiation, and embryogenesis; it interacts with the retinoic acid receptor and retinoic acid X receptor to eventually regulate target gene expression in chordates. RA is transformed from retinaldehyde via oxidization by retinaldehyde dehydrogenase (RALDH), which belongs to the family of oxidoreductases. Several chemicals, including disulphiram, diethylaminobenzaldehyde, and SB-210661, can effectively inhibit RALDH activity, potentially causing reproductive and developmental toxicity. The modes of action can be sequentially explained based on the molecular initiating event toward key events, and finally the adverse outcomes. Adverse outcome pathway (AOP) is a conceptual and theoretical framework that describes the sequential chain of casually liked events at different biological levels from molecular events to adverse effects. In the present review, we discussed a recently registered AOP (AOP(297); inhibition of retinaldehyde dehydrogenase leads to population decline) to explain and support the weight of evidence for RALDH inhibition-related developmental toxicity using the existing knowledge. MDPI 2021-10-20 /pmc/articles/PMC8623920/ /pubmed/34822523 http://dx.doi.org/10.3390/toxins13110739 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Cho, Kichul
Lee, Sang-Moo
Heo, Jina
Kwon, Yong Min
Chung, Dawoon
Yu, Woon-Jong
Bae, Seung Seob
Choi, Grace
Lee, Dae-Sung
Kim, Youngjun
Retinaldehyde Dehydrogenase Inhibition-Related Adverse Outcome Pathway: Potential Risk of Retinoic Acid Synthesis Inhibition during Embryogenesis
title Retinaldehyde Dehydrogenase Inhibition-Related Adverse Outcome Pathway: Potential Risk of Retinoic Acid Synthesis Inhibition during Embryogenesis
title_full Retinaldehyde Dehydrogenase Inhibition-Related Adverse Outcome Pathway: Potential Risk of Retinoic Acid Synthesis Inhibition during Embryogenesis
title_fullStr Retinaldehyde Dehydrogenase Inhibition-Related Adverse Outcome Pathway: Potential Risk of Retinoic Acid Synthesis Inhibition during Embryogenesis
title_full_unstemmed Retinaldehyde Dehydrogenase Inhibition-Related Adverse Outcome Pathway: Potential Risk of Retinoic Acid Synthesis Inhibition during Embryogenesis
title_short Retinaldehyde Dehydrogenase Inhibition-Related Adverse Outcome Pathway: Potential Risk of Retinoic Acid Synthesis Inhibition during Embryogenesis
title_sort retinaldehyde dehydrogenase inhibition-related adverse outcome pathway: potential risk of retinoic acid synthesis inhibition during embryogenesis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8623920/
https://www.ncbi.nlm.nih.gov/pubmed/34822523
http://dx.doi.org/10.3390/toxins13110739
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