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Proline metabolism and cancer: emerging links to glutamine and collagen
PURPOSE OF REVIEW: Proline metabolism impacts a number of regulatory targets in both animals and plants and is especially important in cancer. Glutamine, a related amino acid, is considered second in importance only to glucose as a substrate for tumors. But proline and glutamine are interconvertible...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4255759/ https://www.ncbi.nlm.nih.gov/pubmed/25474014 http://dx.doi.org/10.1097/MCO.0000000000000121 |
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author | Phang, James M. Liu, Wei Hancock, Chad N. Fischer, Joseph W. |
author_facet | Phang, James M. Liu, Wei Hancock, Chad N. Fischer, Joseph W. |
author_sort | Phang, James M. |
collection | PubMed |
description | PURPOSE OF REVIEW: Proline metabolism impacts a number of regulatory targets in both animals and plants and is especially important in cancer. Glutamine, a related amino acid, is considered second in importance only to glucose as a substrate for tumors. But proline and glutamine are interconvertible and linked in their metabolism. In animals, proline and glutamine have specific regulatory functions and their respective physiologic sources. A comparison of the metabolism of proline and glutamine would help us understand the importance of these two nonessential amino acids in cancer metabolism. RECENT FINDINGS: The regulatory functions of proline metabolism proposed 3 decades ago have found relevance in many areas. For cancer, these functions play a role in apoptosis, autophagy and in response to nutrient and oxygen deprivation. Importantly, proline-derived reactive oxygen species served as a driving signal for reprogramming. This model has been applied by others to metabolic regulation for the insulin-prosurvival axis, induction of adipose triglyceride lipase for lipid metabolism and regulation of embryonic stem cell development. Of special interest, modulatory proteins such as parkinson protein 7 and oral cancer overexpressed 1 interact with pyrroline-5-carboxylate reductase, a critical component of the proline regulatory axis. Although the interconvertibility of proline and glutamine has been long established, recent findings showed that the proto-oncogene, cellular myelocytomatosis oncogene, upregulates glutamine utilization (glutaminase) and routes glutamate to proline biosynthesis (pyrroline-5-carboxylate synthase, pyrroline-5-carboxylate reductases). Additionally, collagen, which contains large amounts of proline, may be metabolized to serve as a reservoir for proline. This metabolic relationship as well as the new regulatory targets of proline metabolism invites an elucidation of the differential effects of these nonessential amino acids and their production, storage and mobilization. SUMMARY: Mechanisms by which the proline regulatory axis modulates the cancer phenotype are being revealed. Proline can be synthesized from glutamine as well as derived from collagen degradation. The metabolism of proline serves as a source of energy during stress, provides signaling reactive oxygen species for epigenetic reprogramming and regulates redox homeostasis. |
format | Online Article Text |
id | pubmed-4255759 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-42557592014-12-05 Proline metabolism and cancer: emerging links to glutamine and collagen Phang, James M. Liu, Wei Hancock, Chad N. Fischer, Joseph W. Curr Opin Clin Nutr Metab Care PROTEIN, AMINO ACID METABOLISM AND THERAPY: Edited by Olav Rooyackers and Sidney M. Morris Jr. PURPOSE OF REVIEW: Proline metabolism impacts a number of regulatory targets in both animals and plants and is especially important in cancer. Glutamine, a related amino acid, is considered second in importance only to glucose as a substrate for tumors. But proline and glutamine are interconvertible and linked in their metabolism. In animals, proline and glutamine have specific regulatory functions and their respective physiologic sources. A comparison of the metabolism of proline and glutamine would help us understand the importance of these two nonessential amino acids in cancer metabolism. RECENT FINDINGS: The regulatory functions of proline metabolism proposed 3 decades ago have found relevance in many areas. For cancer, these functions play a role in apoptosis, autophagy and in response to nutrient and oxygen deprivation. Importantly, proline-derived reactive oxygen species served as a driving signal for reprogramming. This model has been applied by others to metabolic regulation for the insulin-prosurvival axis, induction of adipose triglyceride lipase for lipid metabolism and regulation of embryonic stem cell development. Of special interest, modulatory proteins such as parkinson protein 7 and oral cancer overexpressed 1 interact with pyrroline-5-carboxylate reductase, a critical component of the proline regulatory axis. Although the interconvertibility of proline and glutamine has been long established, recent findings showed that the proto-oncogene, cellular myelocytomatosis oncogene, upregulates glutamine utilization (glutaminase) and routes glutamate to proline biosynthesis (pyrroline-5-carboxylate synthase, pyrroline-5-carboxylate reductases). Additionally, collagen, which contains large amounts of proline, may be metabolized to serve as a reservoir for proline. This metabolic relationship as well as the new regulatory targets of proline metabolism invites an elucidation of the differential effects of these nonessential amino acids and their production, storage and mobilization. SUMMARY: Mechanisms by which the proline regulatory axis modulates the cancer phenotype are being revealed. Proline can be synthesized from glutamine as well as derived from collagen degradation. The metabolism of proline serves as a source of energy during stress, provides signaling reactive oxygen species for epigenetic reprogramming and regulates redox homeostasis. Lippincott Williams & Wilkins 2015-01 2014-12-04 /pmc/articles/PMC4255759/ /pubmed/25474014 http://dx.doi.org/10.1097/MCO.0000000000000121 Text en © 2014 Wolters Kluwer Health | Lippincott Williams & Wilkins http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License, where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially. http://creativecommons.org/licenses/by-nc-nd/3.0 |
spellingShingle | PROTEIN, AMINO ACID METABOLISM AND THERAPY: Edited by Olav Rooyackers and Sidney M. Morris Jr. Phang, James M. Liu, Wei Hancock, Chad N. Fischer, Joseph W. Proline metabolism and cancer: emerging links to glutamine and collagen |
title | Proline metabolism and cancer: emerging links to glutamine and collagen |
title_full | Proline metabolism and cancer: emerging links to glutamine and collagen |
title_fullStr | Proline metabolism and cancer: emerging links to glutamine and collagen |
title_full_unstemmed | Proline metabolism and cancer: emerging links to glutamine and collagen |
title_short | Proline metabolism and cancer: emerging links to glutamine and collagen |
title_sort | proline metabolism and cancer: emerging links to glutamine and collagen |
topic | PROTEIN, AMINO ACID METABOLISM AND THERAPY: Edited by Olav Rooyackers and Sidney M. Morris Jr. |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4255759/ https://www.ncbi.nlm.nih.gov/pubmed/25474014 http://dx.doi.org/10.1097/MCO.0000000000000121 |
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