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The Role of AKR1B10 in Physiology and Pathophysiology

AKR1B10 is a human nicotinamide adenine dinucleotide phosphate (NADPH)-dependent reductase belonging to the aldo-keto reductase (AKR) 1B subfamily. It catalyzes the reduction of aldehydes, some ketones and quinones, and interacts with acetyl-CoA carboxylase and heat shock protein 90α. The enzyme is...

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Autores principales: Endo, Satoshi, Matsunaga, Toshiyuki, Nishinaka, Toru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8224097/
https://www.ncbi.nlm.nih.gov/pubmed/34063865
http://dx.doi.org/10.3390/metabo11060332
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author Endo, Satoshi
Matsunaga, Toshiyuki
Nishinaka, Toru
author_facet Endo, Satoshi
Matsunaga, Toshiyuki
Nishinaka, Toru
author_sort Endo, Satoshi
collection PubMed
description AKR1B10 is a human nicotinamide adenine dinucleotide phosphate (NADPH)-dependent reductase belonging to the aldo-keto reductase (AKR) 1B subfamily. It catalyzes the reduction of aldehydes, some ketones and quinones, and interacts with acetyl-CoA carboxylase and heat shock protein 90α. The enzyme is highly expressed in epithelial cells of the stomach and intestine, but down-regulated in gastrointestinal cancers and inflammatory bowel diseases. In contrast, AKR1B10 expression is low in other tissues, where the enzyme is upregulated in cancers, as well as in non-alcoholic fatty liver disease and several skin diseases. In addition, the enzyme’s expression is elevated in cancer cells resistant to clinical anti-cancer drugs. Thus, growing evidence supports AKR1B10 as a potential target for diagnosing and treating these diseases. Herein, we reviewed the literature on the roles of AKR1B10 in a healthy gastrointestinal tract, the development and progression of cancers and acquired chemoresistance, in addition to its gene regulation, functions, and inhibitors.
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spelling pubmed-82240972021-06-25 The Role of AKR1B10 in Physiology and Pathophysiology Endo, Satoshi Matsunaga, Toshiyuki Nishinaka, Toru Metabolites Review AKR1B10 is a human nicotinamide adenine dinucleotide phosphate (NADPH)-dependent reductase belonging to the aldo-keto reductase (AKR) 1B subfamily. It catalyzes the reduction of aldehydes, some ketones and quinones, and interacts with acetyl-CoA carboxylase and heat shock protein 90α. The enzyme is highly expressed in epithelial cells of the stomach and intestine, but down-regulated in gastrointestinal cancers and inflammatory bowel diseases. In contrast, AKR1B10 expression is low in other tissues, where the enzyme is upregulated in cancers, as well as in non-alcoholic fatty liver disease and several skin diseases. In addition, the enzyme’s expression is elevated in cancer cells resistant to clinical anti-cancer drugs. Thus, growing evidence supports AKR1B10 as a potential target for diagnosing and treating these diseases. Herein, we reviewed the literature on the roles of AKR1B10 in a healthy gastrointestinal tract, the development and progression of cancers and acquired chemoresistance, in addition to its gene regulation, functions, and inhibitors. MDPI 2021-05-21 /pmc/articles/PMC8224097/ /pubmed/34063865 http://dx.doi.org/10.3390/metabo11060332 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
Endo, Satoshi
Matsunaga, Toshiyuki
Nishinaka, Toru
The Role of AKR1B10 in Physiology and Pathophysiology
title The Role of AKR1B10 in Physiology and Pathophysiology
title_full The Role of AKR1B10 in Physiology and Pathophysiology
title_fullStr The Role of AKR1B10 in Physiology and Pathophysiology
title_full_unstemmed The Role of AKR1B10 in Physiology and Pathophysiology
title_short The Role of AKR1B10 in Physiology and Pathophysiology
title_sort role of akr1b10 in physiology and pathophysiology
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8224097/
https://www.ncbi.nlm.nih.gov/pubmed/34063865
http://dx.doi.org/10.3390/metabo11060332
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