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2-Deoxy-d-Glucose and Its Analogs: From Diagnostic to Therapeutic Agents
The ability of 2-deoxy-d-glucose (2-DG) to interfere with d-glucose metabolism demonstrates that nutrient and energy deprivation is an efficient tool to suppress cancer cell growth and survival. Acting as a d-glucose mimic, 2-DG inhibits glycolysis due to formation and intracellular accumulation of...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6982256/ https://www.ncbi.nlm.nih.gov/pubmed/31905745 http://dx.doi.org/10.3390/ijms21010234 |
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author | Pajak, B. Siwiak, E. Sołtyka, M. Priebe, A. Zieliński, R. Fokt, I. Ziemniak, M. Jaśkiewicz, A. Borowski, R. Domoradzki, T. Priebe, W. |
author_facet | Pajak, B. Siwiak, E. Sołtyka, M. Priebe, A. Zieliński, R. Fokt, I. Ziemniak, M. Jaśkiewicz, A. Borowski, R. Domoradzki, T. Priebe, W. |
author_sort | Pajak, B. |
collection | PubMed |
description | The ability of 2-deoxy-d-glucose (2-DG) to interfere with d-glucose metabolism demonstrates that nutrient and energy deprivation is an efficient tool to suppress cancer cell growth and survival. Acting as a d-glucose mimic, 2-DG inhibits glycolysis due to formation and intracellular accumulation of 2-deoxy-d-glucose-6-phosphate (2-DG6P), inhibiting the function of hexokinase and glucose-6-phosphate isomerase, and inducing cell death. In addition to glycolysis inhibition, other molecular processes are also affected by 2-DG. Attempts to improve 2-DG’s drug-like properties, its role as a potential adjuvant for other chemotherapeutics, and novel 2-DG analogs as promising new anticancer agents are discussed in this review. |
format | Online Article Text |
id | pubmed-6982256 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-69822562020-02-07 2-Deoxy-d-Glucose and Its Analogs: From Diagnostic to Therapeutic Agents Pajak, B. Siwiak, E. Sołtyka, M. Priebe, A. Zieliński, R. Fokt, I. Ziemniak, M. Jaśkiewicz, A. Borowski, R. Domoradzki, T. Priebe, W. Int J Mol Sci Review The ability of 2-deoxy-d-glucose (2-DG) to interfere with d-glucose metabolism demonstrates that nutrient and energy deprivation is an efficient tool to suppress cancer cell growth and survival. Acting as a d-glucose mimic, 2-DG inhibits glycolysis due to formation and intracellular accumulation of 2-deoxy-d-glucose-6-phosphate (2-DG6P), inhibiting the function of hexokinase and glucose-6-phosphate isomerase, and inducing cell death. In addition to glycolysis inhibition, other molecular processes are also affected by 2-DG. Attempts to improve 2-DG’s drug-like properties, its role as a potential adjuvant for other chemotherapeutics, and novel 2-DG analogs as promising new anticancer agents are discussed in this review. MDPI 2019-12-29 /pmc/articles/PMC6982256/ /pubmed/31905745 http://dx.doi.org/10.3390/ijms21010234 Text en © 2019 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 Pajak, B. Siwiak, E. Sołtyka, M. Priebe, A. Zieliński, R. Fokt, I. Ziemniak, M. Jaśkiewicz, A. Borowski, R. Domoradzki, T. Priebe, W. 2-Deoxy-d-Glucose and Its Analogs: From Diagnostic to Therapeutic Agents |
title | 2-Deoxy-d-Glucose and Its Analogs: From Diagnostic to Therapeutic Agents |
title_full | 2-Deoxy-d-Glucose and Its Analogs: From Diagnostic to Therapeutic Agents |
title_fullStr | 2-Deoxy-d-Glucose and Its Analogs: From Diagnostic to Therapeutic Agents |
title_full_unstemmed | 2-Deoxy-d-Glucose and Its Analogs: From Diagnostic to Therapeutic Agents |
title_short | 2-Deoxy-d-Glucose and Its Analogs: From Diagnostic to Therapeutic Agents |
title_sort | 2-deoxy-d-glucose and its analogs: from diagnostic to therapeutic agents |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6982256/ https://www.ncbi.nlm.nih.gov/pubmed/31905745 http://dx.doi.org/10.3390/ijms21010234 |
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