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Glyoxalase System in the Progression of Skin Aging and Skin Malignancies

Dicarbonyl compounds, including methylglyoxal (MGO) and glyoxal (GO), are mainly formed as byproducts of glucose metabolism. The main glyoxalase system consists of glyoxalase I and II (Glo1 and Glo2) and is the main enzyme involved in the detoxification of dicarbonyl stress, which occurs as an accum...

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Autores principales: Yumnam, Silvia, Subedi, Lalita, Kim, Sun Yeou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7794849/
https://www.ncbi.nlm.nih.gov/pubmed/33396745
http://dx.doi.org/10.3390/ijms22010310
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author Yumnam, Silvia
Subedi, Lalita
Kim, Sun Yeou
author_facet Yumnam, Silvia
Subedi, Lalita
Kim, Sun Yeou
author_sort Yumnam, Silvia
collection PubMed
description Dicarbonyl compounds, including methylglyoxal (MGO) and glyoxal (GO), are mainly formed as byproducts of glucose metabolism. The main glyoxalase system consists of glyoxalase I and II (Glo1 and Glo2) and is the main enzyme involved in the detoxification of dicarbonyl stress, which occurs as an accumulation of MGO or GO due to decreased activity or expression of Glo1. Dicarbonyl stress is a major cause of cellular and tissue dysfunction that causes various health issues, including diabetes, aging, and cancer. The skin is the largest organ in the body. In this review, we discuss the role of the glyoxalase system in the progression of skin aging, and more importantly, skin malignancies. We also discuss the future prospects of the glyoxalase system in other skin abnormalities such as psoriasis and vitiligo, including hyperpigmentation. Finally, in the present review, we suggest the role of glyoxalase in the progression of skin aging and glyoxalase system as a potential target for anticancer drug development for skin cancer.
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spelling pubmed-77948492021-01-10 Glyoxalase System in the Progression of Skin Aging and Skin Malignancies Yumnam, Silvia Subedi, Lalita Kim, Sun Yeou Int J Mol Sci Review Dicarbonyl compounds, including methylglyoxal (MGO) and glyoxal (GO), are mainly formed as byproducts of glucose metabolism. The main glyoxalase system consists of glyoxalase I and II (Glo1 and Glo2) and is the main enzyme involved in the detoxification of dicarbonyl stress, which occurs as an accumulation of MGO or GO due to decreased activity or expression of Glo1. Dicarbonyl stress is a major cause of cellular and tissue dysfunction that causes various health issues, including diabetes, aging, and cancer. The skin is the largest organ in the body. In this review, we discuss the role of the glyoxalase system in the progression of skin aging, and more importantly, skin malignancies. We also discuss the future prospects of the glyoxalase system in other skin abnormalities such as psoriasis and vitiligo, including hyperpigmentation. Finally, in the present review, we suggest the role of glyoxalase in the progression of skin aging and glyoxalase system as a potential target for anticancer drug development for skin cancer. MDPI 2020-12-30 /pmc/articles/PMC7794849/ /pubmed/33396745 http://dx.doi.org/10.3390/ijms22010310 Text en © 2020 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
Yumnam, Silvia
Subedi, Lalita
Kim, Sun Yeou
Glyoxalase System in the Progression of Skin Aging and Skin Malignancies
title Glyoxalase System in the Progression of Skin Aging and Skin Malignancies
title_full Glyoxalase System in the Progression of Skin Aging and Skin Malignancies
title_fullStr Glyoxalase System in the Progression of Skin Aging and Skin Malignancies
title_full_unstemmed Glyoxalase System in the Progression of Skin Aging and Skin Malignancies
title_short Glyoxalase System in the Progression of Skin Aging and Skin Malignancies
title_sort glyoxalase system in the progression of skin aging and skin malignancies
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7794849/
https://www.ncbi.nlm.nih.gov/pubmed/33396745
http://dx.doi.org/10.3390/ijms22010310
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