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Energy Metabolic Plasticity of Colorectal Cancer Cells as a Determinant of Tumor Growth and Metastasis
Metabolic plasticity is the ability of the cell to adjust its metabolism to changes in environmental conditions. Increased metabolic plasticity is a defining characteristic of cancer cells, which gives them the advantage of survival and a higher proliferative capacity. Here we review some functional...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8351413/ https://www.ncbi.nlm.nih.gov/pubmed/34381722 http://dx.doi.org/10.3389/fonc.2021.698951 |
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author | Reinsalu, Leenu Puurand, Marju Chekulayev, Vladimir Miller, Sten Shevchuk, Igor Tepp, Kersti Rebane-Klemm, Egle Timohhina, Natalja Terasmaa, Anton Kaambre, Tuuli |
author_facet | Reinsalu, Leenu Puurand, Marju Chekulayev, Vladimir Miller, Sten Shevchuk, Igor Tepp, Kersti Rebane-Klemm, Egle Timohhina, Natalja Terasmaa, Anton Kaambre, Tuuli |
author_sort | Reinsalu, Leenu |
collection | PubMed |
description | Metabolic plasticity is the ability of the cell to adjust its metabolism to changes in environmental conditions. Increased metabolic plasticity is a defining characteristic of cancer cells, which gives them the advantage of survival and a higher proliferative capacity. Here we review some functional features of metabolic plasticity of colorectal cancer cells (CRC). Metabolic plasticity is characterized by changes in adenine nucleotide transport across the outer mitochondrial membrane. Voltage-dependent anion channel (VDAC) is the main protein involved in the transport of adenine nucleotides, and its regulation is impaired in CRC cells. Apparent affinity for ADP is a functional parameter that characterizes VDAC permeability and provides an integrated assessment of cell metabolic state. VDAC permeability can be adjusted via its interactions with other proteins, such as hexokinase and tubulin. Also, the redox conditions inside a cancer cell may alter VDAC function, resulting in enhanced metabolic plasticity. In addition, a cancer cell shows reprogrammed energy transfer circuits such as adenylate kinase (AK) and creatine kinase (CK) pathway. Knowledge of the mechanism of metabolic plasticity will improve our understanding of colorectal carcinogenesis. |
format | Online Article Text |
id | pubmed-8351413 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83514132021-08-10 Energy Metabolic Plasticity of Colorectal Cancer Cells as a Determinant of Tumor Growth and Metastasis Reinsalu, Leenu Puurand, Marju Chekulayev, Vladimir Miller, Sten Shevchuk, Igor Tepp, Kersti Rebane-Klemm, Egle Timohhina, Natalja Terasmaa, Anton Kaambre, Tuuli Front Oncol Oncology Metabolic plasticity is the ability of the cell to adjust its metabolism to changes in environmental conditions. Increased metabolic plasticity is a defining characteristic of cancer cells, which gives them the advantage of survival and a higher proliferative capacity. Here we review some functional features of metabolic plasticity of colorectal cancer cells (CRC). Metabolic plasticity is characterized by changes in adenine nucleotide transport across the outer mitochondrial membrane. Voltage-dependent anion channel (VDAC) is the main protein involved in the transport of adenine nucleotides, and its regulation is impaired in CRC cells. Apparent affinity for ADP is a functional parameter that characterizes VDAC permeability and provides an integrated assessment of cell metabolic state. VDAC permeability can be adjusted via its interactions with other proteins, such as hexokinase and tubulin. Also, the redox conditions inside a cancer cell may alter VDAC function, resulting in enhanced metabolic plasticity. In addition, a cancer cell shows reprogrammed energy transfer circuits such as adenylate kinase (AK) and creatine kinase (CK) pathway. Knowledge of the mechanism of metabolic plasticity will improve our understanding of colorectal carcinogenesis. Frontiers Media S.A. 2021-07-26 /pmc/articles/PMC8351413/ /pubmed/34381722 http://dx.doi.org/10.3389/fonc.2021.698951 Text en Copyright © 2021 Reinsalu, Puurand, Chekulayev, Miller, Shevchuk, Tepp, Rebane-Klemm, Timohhina, Terasmaa and Kaambre 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 Reinsalu, Leenu Puurand, Marju Chekulayev, Vladimir Miller, Sten Shevchuk, Igor Tepp, Kersti Rebane-Klemm, Egle Timohhina, Natalja Terasmaa, Anton Kaambre, Tuuli Energy Metabolic Plasticity of Colorectal Cancer Cells as a Determinant of Tumor Growth and Metastasis |
title | Energy Metabolic Plasticity of Colorectal Cancer Cells as a Determinant of Tumor Growth and Metastasis |
title_full | Energy Metabolic Plasticity of Colorectal Cancer Cells as a Determinant of Tumor Growth and Metastasis |
title_fullStr | Energy Metabolic Plasticity of Colorectal Cancer Cells as a Determinant of Tumor Growth and Metastasis |
title_full_unstemmed | Energy Metabolic Plasticity of Colorectal Cancer Cells as a Determinant of Tumor Growth and Metastasis |
title_short | Energy Metabolic Plasticity of Colorectal Cancer Cells as a Determinant of Tumor Growth and Metastasis |
title_sort | energy metabolic plasticity of colorectal cancer cells as a determinant of tumor growth and metastasis |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8351413/ https://www.ncbi.nlm.nih.gov/pubmed/34381722 http://dx.doi.org/10.3389/fonc.2021.698951 |
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