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Targeting cancer-specific metabolic pathways for developing novel cancer therapeutics
Cancer is a heterogeneous disease characterized by various genetic and phenotypic aberrations. Cancer cells undergo genetic modifications that promote their proliferation, survival, and dissemination as the disease progresses. The unabated proliferation of cancer cells incurs an enormous energy dema...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9815821/ https://www.ncbi.nlm.nih.gov/pubmed/36618350 http://dx.doi.org/10.3389/fimmu.2022.955476 |
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author | Pal, Soumik Sharma, Amit Mathew, Sam Padalumavunkal Jaganathan, Bithiah Grace |
author_facet | Pal, Soumik Sharma, Amit Mathew, Sam Padalumavunkal Jaganathan, Bithiah Grace |
author_sort | Pal, Soumik |
collection | PubMed |
description | Cancer is a heterogeneous disease characterized by various genetic and phenotypic aberrations. Cancer cells undergo genetic modifications that promote their proliferation, survival, and dissemination as the disease progresses. The unabated proliferation of cancer cells incurs an enormous energy demand that is supplied by metabolic reprogramming. Cancer cells undergo metabolic alterations to provide for increased energy and metabolite requirement; these alterations also help drive the tumor progression. Dysregulation in glucose uptake and increased lactate production via “aerobic glycolysis” were described more than 100 years ago, and since then, the metabolic signature of various cancers has been extensively studied. However, the extensive research in this field has failed to translate into significant therapeutic intervention, except for treating childhood-ALL with amino acid metabolism inhibitor L-asparaginase. Despite the growing understanding of novel metabolic alterations in tumors, the therapeutic targeting of these tumor-specific dysregulations has largely been ineffective in clinical trials. This chapter discusses the major pathways involved in the metabolism of glucose, amino acids, and lipids and highlights the inter-twined nature of metabolic aberrations that promote tumorigenesis in different types of cancer. Finally, we summarise the therapeutic interventions which can be used as a combinational therapy to target metabolic dysregulations that are unique or common in blood, breast, colorectal, lung, and prostate cancer. |
format | Online Article Text |
id | pubmed-9815821 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98158212023-01-06 Targeting cancer-specific metabolic pathways for developing novel cancer therapeutics Pal, Soumik Sharma, Amit Mathew, Sam Padalumavunkal Jaganathan, Bithiah Grace Front Immunol Immunology Cancer is a heterogeneous disease characterized by various genetic and phenotypic aberrations. Cancer cells undergo genetic modifications that promote their proliferation, survival, and dissemination as the disease progresses. The unabated proliferation of cancer cells incurs an enormous energy demand that is supplied by metabolic reprogramming. Cancer cells undergo metabolic alterations to provide for increased energy and metabolite requirement; these alterations also help drive the tumor progression. Dysregulation in glucose uptake and increased lactate production via “aerobic glycolysis” were described more than 100 years ago, and since then, the metabolic signature of various cancers has been extensively studied. However, the extensive research in this field has failed to translate into significant therapeutic intervention, except for treating childhood-ALL with amino acid metabolism inhibitor L-asparaginase. Despite the growing understanding of novel metabolic alterations in tumors, the therapeutic targeting of these tumor-specific dysregulations has largely been ineffective in clinical trials. This chapter discusses the major pathways involved in the metabolism of glucose, amino acids, and lipids and highlights the inter-twined nature of metabolic aberrations that promote tumorigenesis in different types of cancer. Finally, we summarise the therapeutic interventions which can be used as a combinational therapy to target metabolic dysregulations that are unique or common in blood, breast, colorectal, lung, and prostate cancer. Frontiers Media S.A. 2022-12-22 /pmc/articles/PMC9815821/ /pubmed/36618350 http://dx.doi.org/10.3389/fimmu.2022.955476 Text en Copyright © 2022 Pal, Sharma, Mathew and Jaganathan 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 | Immunology Pal, Soumik Sharma, Amit Mathew, Sam Padalumavunkal Jaganathan, Bithiah Grace Targeting cancer-specific metabolic pathways for developing novel cancer therapeutics |
title | Targeting cancer-specific metabolic pathways for developing novel cancer therapeutics |
title_full | Targeting cancer-specific metabolic pathways for developing novel cancer therapeutics |
title_fullStr | Targeting cancer-specific metabolic pathways for developing novel cancer therapeutics |
title_full_unstemmed | Targeting cancer-specific metabolic pathways for developing novel cancer therapeutics |
title_short | Targeting cancer-specific metabolic pathways for developing novel cancer therapeutics |
title_sort | targeting cancer-specific metabolic pathways for developing novel cancer therapeutics |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9815821/ https://www.ncbi.nlm.nih.gov/pubmed/36618350 http://dx.doi.org/10.3389/fimmu.2022.955476 |
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