维甲酸
内科学
畸形学
内分泌学
维甲酸
胚胎
癌症研究
还原酶
医学
异维甲酸
药理学
生物化学
作者
Kichul Cho,Sang-Moo Lee,Jina Heo,Yong Hyun Kwon,Dawoon Chung,Woon-Jong Yu,Seung Seob Bae,Grace Choi,Daesung Lee,Da‐Hye Kim
出处
期刊:Toxins
[Multidisciplinary Digital Publishing Institute]
日期:2021-10-20
卷期号:13 (11): 739-739
被引量:3
标识
DOI:10.3390/toxins13110739
摘要
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 (AOP297; 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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