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RING-finger E3 ligases regulatory network in PI3K/AKT-mediated glucose metabolism

The phosphatidylinositol 3-kinase (PI3K)/AKT signaling pathway plays an essential role in glucose metabolism, promoting glycolysis and resisting gluconeogenesis. PI3K/AKT signaling can directly alter glucose metabolism by phosphorylating several metabolic enzymes or regulators of nutrient transport....

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Autores principales: Wang, Wenke, Shi, Bei, Cong, Ruiting, Hao, Mingjun, Peng, Yuanyuan, Yang, Hongyue, Song, Jiahui, Feng, Di, Zhang, Naijin, Li, Da
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9402544/
https://www.ncbi.nlm.nih.gov/pubmed/36002460
http://dx.doi.org/10.1038/s41420-022-01162-7
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author Wang, Wenke
Shi, Bei
Cong, Ruiting
Hao, Mingjun
Peng, Yuanyuan
Yang, Hongyue
Song, Jiahui
Feng, Di
Zhang, Naijin
Li, Da
author_facet Wang, Wenke
Shi, Bei
Cong, Ruiting
Hao, Mingjun
Peng, Yuanyuan
Yang, Hongyue
Song, Jiahui
Feng, Di
Zhang, Naijin
Li, Da
author_sort Wang, Wenke
collection PubMed
description The phosphatidylinositol 3-kinase (PI3K)/AKT signaling pathway plays an essential role in glucose metabolism, promoting glycolysis and resisting gluconeogenesis. PI3K/AKT signaling can directly alter glucose metabolism by phosphorylating several metabolic enzymes or regulators of nutrient transport. It can indirectly promote sustained aerobic glycolysis by increasing glucose transporters and glycolytic enzymes, which are mediated by downstream transcription factors. E3 ubiquitin ligase RING-finger proteins are mediators of protein post-translational modifications and include the cullin-RING ligase complexes, the tumor necrosis factor receptor-associated family, the tripartite motif family and etc. Some members of the RING family play critical roles in regulating cell signaling and are involved in the development and progression of various metabolic diseases, such as cancer, diabetes, and dyslipidemia. And with the progression of modern research, as a negative or active regulator, the RING-finger adaptor has been found to play an indispensable role in PI3K/AKT signaling. However, no reviews have comprehensively clarified the role of RING-finger E3 ligases in PI3K/AKT-mediated glucose metabolism. Therefore, in this review, we focus on the regulation and function of RING ligases in PI3K/AKT-mediated glucose metabolism to establish new insights into the prevention and treatment of metabolic diseases.
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spelling pubmed-94025442022-08-26 RING-finger E3 ligases regulatory network in PI3K/AKT-mediated glucose metabolism Wang, Wenke Shi, Bei Cong, Ruiting Hao, Mingjun Peng, Yuanyuan Yang, Hongyue Song, Jiahui Feng, Di Zhang, Naijin Li, Da Cell Death Discov Review Article The phosphatidylinositol 3-kinase (PI3K)/AKT signaling pathway plays an essential role in glucose metabolism, promoting glycolysis and resisting gluconeogenesis. PI3K/AKT signaling can directly alter glucose metabolism by phosphorylating several metabolic enzymes or regulators of nutrient transport. It can indirectly promote sustained aerobic glycolysis by increasing glucose transporters and glycolytic enzymes, which are mediated by downstream transcription factors. E3 ubiquitin ligase RING-finger proteins are mediators of protein post-translational modifications and include the cullin-RING ligase complexes, the tumor necrosis factor receptor-associated family, the tripartite motif family and etc. Some members of the RING family play critical roles in regulating cell signaling and are involved in the development and progression of various metabolic diseases, such as cancer, diabetes, and dyslipidemia. And with the progression of modern research, as a negative or active regulator, the RING-finger adaptor has been found to play an indispensable role in PI3K/AKT signaling. However, no reviews have comprehensively clarified the role of RING-finger E3 ligases in PI3K/AKT-mediated glucose metabolism. Therefore, in this review, we focus on the regulation and function of RING ligases in PI3K/AKT-mediated glucose metabolism to establish new insights into the prevention and treatment of metabolic diseases. Nature Publishing Group UK 2022-08-24 /pmc/articles/PMC9402544/ /pubmed/36002460 http://dx.doi.org/10.1038/s41420-022-01162-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review Article
Wang, Wenke
Shi, Bei
Cong, Ruiting
Hao, Mingjun
Peng, Yuanyuan
Yang, Hongyue
Song, Jiahui
Feng, Di
Zhang, Naijin
Li, Da
RING-finger E3 ligases regulatory network in PI3K/AKT-mediated glucose metabolism
title RING-finger E3 ligases regulatory network in PI3K/AKT-mediated glucose metabolism
title_full RING-finger E3 ligases regulatory network in PI3K/AKT-mediated glucose metabolism
title_fullStr RING-finger E3 ligases regulatory network in PI3K/AKT-mediated glucose metabolism
title_full_unstemmed RING-finger E3 ligases regulatory network in PI3K/AKT-mediated glucose metabolism
title_short RING-finger E3 ligases regulatory network in PI3K/AKT-mediated glucose metabolism
title_sort ring-finger e3 ligases regulatory network in pi3k/akt-mediated glucose metabolism
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9402544/
https://www.ncbi.nlm.nih.gov/pubmed/36002460
http://dx.doi.org/10.1038/s41420-022-01162-7
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