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Targeting FBPase is an emerging novel approach for cancer therapy

Cancer is a leading cause of death in both developed and developing countries. Metabolic reprogramming is an emerging hallmark of cancer. Glucose homeostasis is reciprocally controlled by the catabolic glycolysis and anabolic gluconeogenesis pathways. Previous studies have mainly focused on cataboli...

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Autores principales: Liu, Gao-Min, Zhang, Yao-Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5845355/
https://www.ncbi.nlm.nih.gov/pubmed/29556139
http://dx.doi.org/10.1186/s12935-018-0533-z
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author Liu, Gao-Min
Zhang, Yao-Ming
author_facet Liu, Gao-Min
Zhang, Yao-Ming
author_sort Liu, Gao-Min
collection PubMed
description Cancer is a leading cause of death in both developed and developing countries. Metabolic reprogramming is an emerging hallmark of cancer. Glucose homeostasis is reciprocally controlled by the catabolic glycolysis and anabolic gluconeogenesis pathways. Previous studies have mainly focused on catabolic glycolysis, but recently, FBPase, a rate-limiting enzyme in gluconeogenesis, was found to play critical roles in tumour initiation and progression in several cancer types. Here, we review recent ideas and discoveries that illustrate the clinical significance of FBPase expression in various cancers, the mechanism through which FBPase influences cancer, and the mechanism of FBPase silencing. Furthermore, we summarize some of the drugs targeting FBPase and discuss their potential use in clinical applications and the problems that remain unsolved.
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spelling pubmed-58453552018-03-19 Targeting FBPase is an emerging novel approach for cancer therapy Liu, Gao-Min Zhang, Yao-Ming Cancer Cell Int Review Cancer is a leading cause of death in both developed and developing countries. Metabolic reprogramming is an emerging hallmark of cancer. Glucose homeostasis is reciprocally controlled by the catabolic glycolysis and anabolic gluconeogenesis pathways. Previous studies have mainly focused on catabolic glycolysis, but recently, FBPase, a rate-limiting enzyme in gluconeogenesis, was found to play critical roles in tumour initiation and progression in several cancer types. Here, we review recent ideas and discoveries that illustrate the clinical significance of FBPase expression in various cancers, the mechanism through which FBPase influences cancer, and the mechanism of FBPase silencing. Furthermore, we summarize some of the drugs targeting FBPase and discuss their potential use in clinical applications and the problems that remain unsolved. BioMed Central 2018-03-09 /pmc/articles/PMC5845355/ /pubmed/29556139 http://dx.doi.org/10.1186/s12935-018-0533-z Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Liu, Gao-Min
Zhang, Yao-Ming
Targeting FBPase is an emerging novel approach for cancer therapy
title Targeting FBPase is an emerging novel approach for cancer therapy
title_full Targeting FBPase is an emerging novel approach for cancer therapy
title_fullStr Targeting FBPase is an emerging novel approach for cancer therapy
title_full_unstemmed Targeting FBPase is an emerging novel approach for cancer therapy
title_short Targeting FBPase is an emerging novel approach for cancer therapy
title_sort targeting fbpase is an emerging novel approach for cancer therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5845355/
https://www.ncbi.nlm.nih.gov/pubmed/29556139
http://dx.doi.org/10.1186/s12935-018-0533-z
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