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Glucometabolic reprogramming: From trigger to therapeutic target in hepatocellular carcinoma

Glucose, the central macronutrient, releases energy as ATP through carbon bond oxidation and supports various physiological functions of living organisms. Hepatocarcinogenesis relies on the bioenergetic advantage conferred by glucometabolic reprogramming. The exploitation of reformed metabolism indu...

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Autores principales: Xia, Haoming, Huang, Ziyue, Wang, Zhensheng, Liu, Shuqiang, Zhao, Xudong, You, Junqi, Xu, Yi, Yam, Judy Wai Ping, Cui, Yunfu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9336635/
https://www.ncbi.nlm.nih.gov/pubmed/35912218
http://dx.doi.org/10.3389/fonc.2022.953668
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author Xia, Haoming
Huang, Ziyue
Wang, Zhensheng
Liu, Shuqiang
Zhao, Xudong
You, Junqi
Xu, Yi
Yam, Judy Wai Ping
Cui, Yunfu
author_facet Xia, Haoming
Huang, Ziyue
Wang, Zhensheng
Liu, Shuqiang
Zhao, Xudong
You, Junqi
Xu, Yi
Yam, Judy Wai Ping
Cui, Yunfu
author_sort Xia, Haoming
collection PubMed
description Glucose, the central macronutrient, releases energy as ATP through carbon bond oxidation and supports various physiological functions of living organisms. Hepatocarcinogenesis relies on the bioenergetic advantage conferred by glucometabolic reprogramming. The exploitation of reformed metabolism induces a uniquely inert environment conducive to survival and renders the hepatocellular carcinoma (HCC) cells the extraordinary ability to thrive even in the nutrient-poor tumor microenvironment. The rewired metabolism also confers a defensive barrier which protects the HCC cells from environmental stress and immune surveillance. Additionally, targeted interventions against key players of HCC metabolic and signaling pathways provide promising prospects for tumor therapy. The active search for novel drugs based on innovative mutation targets is warranted in the future for effectively treating advanced HCC and the preoperative downstage. This article aims to review the regulatory mechanisms and therapeutic value of glucometabolic reprogramming on the disease progression of HCC, to gain insights into basic and clinical research.
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spelling pubmed-93366352022-07-30 Glucometabolic reprogramming: From trigger to therapeutic target in hepatocellular carcinoma Xia, Haoming Huang, Ziyue Wang, Zhensheng Liu, Shuqiang Zhao, Xudong You, Junqi Xu, Yi Yam, Judy Wai Ping Cui, Yunfu Front Oncol Oncology Glucose, the central macronutrient, releases energy as ATP through carbon bond oxidation and supports various physiological functions of living organisms. Hepatocarcinogenesis relies on the bioenergetic advantage conferred by glucometabolic reprogramming. The exploitation of reformed metabolism induces a uniquely inert environment conducive to survival and renders the hepatocellular carcinoma (HCC) cells the extraordinary ability to thrive even in the nutrient-poor tumor microenvironment. The rewired metabolism also confers a defensive barrier which protects the HCC cells from environmental stress and immune surveillance. Additionally, targeted interventions against key players of HCC metabolic and signaling pathways provide promising prospects for tumor therapy. The active search for novel drugs based on innovative mutation targets is warranted in the future for effectively treating advanced HCC and the preoperative downstage. This article aims to review the regulatory mechanisms and therapeutic value of glucometabolic reprogramming on the disease progression of HCC, to gain insights into basic and clinical research. Frontiers Media S.A. 2022-07-15 /pmc/articles/PMC9336635/ /pubmed/35912218 http://dx.doi.org/10.3389/fonc.2022.953668 Text en Copyright © 2022 Xia, Huang, Wang, Liu, Zhao, You, Xu, Yam and Cui https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Xia, Haoming
Huang, Ziyue
Wang, Zhensheng
Liu, Shuqiang
Zhao, Xudong
You, Junqi
Xu, Yi
Yam, Judy Wai Ping
Cui, Yunfu
Glucometabolic reprogramming: From trigger to therapeutic target in hepatocellular carcinoma
title Glucometabolic reprogramming: From trigger to therapeutic target in hepatocellular carcinoma
title_full Glucometabolic reprogramming: From trigger to therapeutic target in hepatocellular carcinoma
title_fullStr Glucometabolic reprogramming: From trigger to therapeutic target in hepatocellular carcinoma
title_full_unstemmed Glucometabolic reprogramming: From trigger to therapeutic target in hepatocellular carcinoma
title_short Glucometabolic reprogramming: From trigger to therapeutic target in hepatocellular carcinoma
title_sort glucometabolic reprogramming: from trigger to therapeutic target in hepatocellular carcinoma
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9336635/
https://www.ncbi.nlm.nih.gov/pubmed/35912218
http://dx.doi.org/10.3389/fonc.2022.953668
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