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Understanding the molecular mechanisms of macrophage polarization and metabolic reprogramming in endometriosis: A narrative review
BACKGROUND: Endometriosis is an estrogen‐dependent disease and causes pelvic pain and infertility. The limits of current pharmacotherapy in women who desire to become pregnant prompt the development of various targeted molecules for more effective treatment. A review article focused on the unique as...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9596393/ https://www.ncbi.nlm.nih.gov/pubmed/36310658 http://dx.doi.org/10.1002/rmb2.12488 |
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author | Kobayashi, Hiroshi Imanaka, Shogo |
author_facet | Kobayashi, Hiroshi Imanaka, Shogo |
author_sort | Kobayashi, Hiroshi |
collection | PubMed |
description | BACKGROUND: Endometriosis is an estrogen‐dependent disease and causes pelvic pain and infertility. The limits of current pharmacotherapy in women who desire to become pregnant prompt the development of various targeted molecules for more effective treatment. A review article focused on the unique aspect of cellular metabolic reprogramming of endometriotic cells has been reported. The cellular metabolic pathways are reprogrammed to adapt to a variety of environmental stresses (e.g., nutrient starvation or glucose deprivation, hypoxic stress, excessive reactive oxygen species generation, and other environmental factors). This review aims to summarize macrophage polarization and metabolic reprogramming in endometriosis. METHODS: A literature search was performed between January 2000 and March 2022 in the PubMed and Google Scholar databases using a combination of specific terms. RESULTS: Macrophage cellular metabolism has a marked influence on its phenotype and function. Preclinical studies showed that metabolic conversion toward glycolysis or oxidative phosphorylation drives macrophage polarization to M1 or M2 phenotype, respectively. Such cellular metabolic rewiring can offer new therapeutic opportunities. CONCLUSION: A better understanding of metabolic reprogramming biology in endometriosis‐associated macrophages is essential in considering novel therapeutic approach for endometriosis. However, there are currently no detailed studies on therapeutic strategies targeting the cellular metabolic properties of endometriosis‐associated macrophages. |
format | Online Article Text |
id | pubmed-9596393 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95963932022-10-27 Understanding the molecular mechanisms of macrophage polarization and metabolic reprogramming in endometriosis: A narrative review Kobayashi, Hiroshi Imanaka, Shogo Reprod Med Biol Reviews BACKGROUND: Endometriosis is an estrogen‐dependent disease and causes pelvic pain and infertility. The limits of current pharmacotherapy in women who desire to become pregnant prompt the development of various targeted molecules for more effective treatment. A review article focused on the unique aspect of cellular metabolic reprogramming of endometriotic cells has been reported. The cellular metabolic pathways are reprogrammed to adapt to a variety of environmental stresses (e.g., nutrient starvation or glucose deprivation, hypoxic stress, excessive reactive oxygen species generation, and other environmental factors). This review aims to summarize macrophage polarization and metabolic reprogramming in endometriosis. METHODS: A literature search was performed between January 2000 and March 2022 in the PubMed and Google Scholar databases using a combination of specific terms. RESULTS: Macrophage cellular metabolism has a marked influence on its phenotype and function. Preclinical studies showed that metabolic conversion toward glycolysis or oxidative phosphorylation drives macrophage polarization to M1 or M2 phenotype, respectively. Such cellular metabolic rewiring can offer new therapeutic opportunities. CONCLUSION: A better understanding of metabolic reprogramming biology in endometriosis‐associated macrophages is essential in considering novel therapeutic approach for endometriosis. However, there are currently no detailed studies on therapeutic strategies targeting the cellular metabolic properties of endometriosis‐associated macrophages. John Wiley and Sons Inc. 2022-10-17 /pmc/articles/PMC9596393/ /pubmed/36310658 http://dx.doi.org/10.1002/rmb2.12488 Text en © 2022 The Authors. Reproductive Medicine and Biology published by John Wiley & Sons Australia, Ltd on behalf of Japan Society for Reproductive Medicine. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Reviews Kobayashi, Hiroshi Imanaka, Shogo Understanding the molecular mechanisms of macrophage polarization and metabolic reprogramming in endometriosis: A narrative review |
title | Understanding the molecular mechanisms of macrophage polarization and metabolic reprogramming in endometriosis: A narrative review |
title_full | Understanding the molecular mechanisms of macrophage polarization and metabolic reprogramming in endometriosis: A narrative review |
title_fullStr | Understanding the molecular mechanisms of macrophage polarization and metabolic reprogramming in endometriosis: A narrative review |
title_full_unstemmed | Understanding the molecular mechanisms of macrophage polarization and metabolic reprogramming in endometriosis: A narrative review |
title_short | Understanding the molecular mechanisms of macrophage polarization and metabolic reprogramming in endometriosis: A narrative review |
title_sort | understanding the molecular mechanisms of macrophage polarization and metabolic reprogramming in endometriosis: a narrative review |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9596393/ https://www.ncbi.nlm.nih.gov/pubmed/36310658 http://dx.doi.org/10.1002/rmb2.12488 |
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