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A New Perspective on the Heterogeneity of Cancer Glycolysis
Tumors are dynamic metabolic systems which highly augmented metabolic fluxes and nutrient needs to support cellular proliferation and physiological function. For many years, a central hallmark of tumor metabolism has emphasized a uniformly elevated aerobic glycolysis as a critical feature of tumorig...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society of Applied Pharmacology
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5746033/ https://www.ncbi.nlm.nih.gov/pubmed/29212302 http://dx.doi.org/10.4062/biomolther.2017.210 |
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author | Neugent, Michael L. Goodwin, Justin Sankaranarayanan, Ishwarya Yetkin, Celal Emre Hsieh, Meng-Hsiung Kim, Jung-whan |
author_facet | Neugent, Michael L. Goodwin, Justin Sankaranarayanan, Ishwarya Yetkin, Celal Emre Hsieh, Meng-Hsiung Kim, Jung-whan |
author_sort | Neugent, Michael L. |
collection | PubMed |
description | Tumors are dynamic metabolic systems which highly augmented metabolic fluxes and nutrient needs to support cellular proliferation and physiological function. For many years, a central hallmark of tumor metabolism has emphasized a uniformly elevated aerobic glycolysis as a critical feature of tumorigenecity. This led to extensive efforts of targeting glycolysis in human cancers. However, clinical attempts to target glycolysis and glucose metabolism have proven to be challenging. Recent advancements revealing a high degree of metabolic heterogeneity and plasticity embedded among various human cancers may paint a new picture of metabolic targeting for cancer therapies with a renewed interest in glucose metabolism. In this review, we will discuss diverse oncogenic and molecular alterations that drive distinct and heterogeneous glucose metabolism in cancers. We will also discuss a new perspective on how aberrantly altered glycolysis in response to oncogenic signaling is further influenced and remodeled by dynamic metabolic interaction with surrounding tumor-associated stromal cells. |
format | Online Article Text |
id | pubmed-5746033 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Korean Society of Applied Pharmacology |
record_format | MEDLINE/PubMed |
spelling | pubmed-57460332018-01-01 A New Perspective on the Heterogeneity of Cancer Glycolysis Neugent, Michael L. Goodwin, Justin Sankaranarayanan, Ishwarya Yetkin, Celal Emre Hsieh, Meng-Hsiung Kim, Jung-whan Biomol Ther (Seoul) Invited Review Tumors are dynamic metabolic systems which highly augmented metabolic fluxes and nutrient needs to support cellular proliferation and physiological function. For many years, a central hallmark of tumor metabolism has emphasized a uniformly elevated aerobic glycolysis as a critical feature of tumorigenecity. This led to extensive efforts of targeting glycolysis in human cancers. However, clinical attempts to target glycolysis and glucose metabolism have proven to be challenging. Recent advancements revealing a high degree of metabolic heterogeneity and plasticity embedded among various human cancers may paint a new picture of metabolic targeting for cancer therapies with a renewed interest in glucose metabolism. In this review, we will discuss diverse oncogenic and molecular alterations that drive distinct and heterogeneous glucose metabolism in cancers. We will also discuss a new perspective on how aberrantly altered glycolysis in response to oncogenic signaling is further influenced and remodeled by dynamic metabolic interaction with surrounding tumor-associated stromal cells. The Korean Society of Applied Pharmacology 2018-01 2017-12-07 /pmc/articles/PMC5746033/ /pubmed/29212302 http://dx.doi.org/10.4062/biomolther.2017.210 Text en Copyright ©2018, The Korean Society of Applied Pharmacology http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Invited Review Neugent, Michael L. Goodwin, Justin Sankaranarayanan, Ishwarya Yetkin, Celal Emre Hsieh, Meng-Hsiung Kim, Jung-whan A New Perspective on the Heterogeneity of Cancer Glycolysis |
title | A New Perspective on the Heterogeneity of Cancer Glycolysis |
title_full | A New Perspective on the Heterogeneity of Cancer Glycolysis |
title_fullStr | A New Perspective on the Heterogeneity of Cancer Glycolysis |
title_full_unstemmed | A New Perspective on the Heterogeneity of Cancer Glycolysis |
title_short | A New Perspective on the Heterogeneity of Cancer Glycolysis |
title_sort | new perspective on the heterogeneity of cancer glycolysis |
topic | Invited Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5746033/ https://www.ncbi.nlm.nih.gov/pubmed/29212302 http://dx.doi.org/10.4062/biomolther.2017.210 |
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