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Therapeutic Metabolic Reprograming Using microRNAs: From Cancer to HIV Infection
MicroRNAs (miRNAs) are crucial regulators of cellular processes, including metabolism. Attempts to use miRNAs as therapeutic agents are being explored in several areas, including the control of cancer progression. Recent evidence suggests fine tuning miRNA activity to reprogram tumor cell metabolism...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8872267/ https://www.ncbi.nlm.nih.gov/pubmed/35205318 http://dx.doi.org/10.3390/genes13020273 |
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author | Gibson, Mark S. Noronha-Estima, Cláudia Gama-Carvalho, Margarida |
author_facet | Gibson, Mark S. Noronha-Estima, Cláudia Gama-Carvalho, Margarida |
author_sort | Gibson, Mark S. |
collection | PubMed |
description | MicroRNAs (miRNAs) are crucial regulators of cellular processes, including metabolism. Attempts to use miRNAs as therapeutic agents are being explored in several areas, including the control of cancer progression. Recent evidence suggests fine tuning miRNA activity to reprogram tumor cell metabolism has enormous potential as an alternative treatment option. Indeed, cancer growth is known to be linked to profound metabolic changes. Likewise, the emerging field of immunometabolism is leading to a refined understanding of how immune cell proliferation and function is governed by glucose homeostasis. Different immune cell types are now known to have unique metabolic signatures that switch in response to a changing environment. T-cell subsets exhibit distinct metabolic profiles which underlie their alternative differentiation and phenotypic functions. Recent evidence shows that the susceptibility of CD4(+) T-cells to HIV infection is intimately linked to their metabolic activity, with many of the metabolic features of HIV-1-infected cells resembling those found in tumor cells. In this review, we discuss the use of miRNA modulation to achieve metabolic reprogramming for cancer therapy and explore the idea that the same approach may serve as an effective mechanism to restrict HIV replication and eliminate infected cells. |
format | Online Article Text |
id | pubmed-8872267 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-88722672022-02-25 Therapeutic Metabolic Reprograming Using microRNAs: From Cancer to HIV Infection Gibson, Mark S. Noronha-Estima, Cláudia Gama-Carvalho, Margarida Genes (Basel) Review MicroRNAs (miRNAs) are crucial regulators of cellular processes, including metabolism. Attempts to use miRNAs as therapeutic agents are being explored in several areas, including the control of cancer progression. Recent evidence suggests fine tuning miRNA activity to reprogram tumor cell metabolism has enormous potential as an alternative treatment option. Indeed, cancer growth is known to be linked to profound metabolic changes. Likewise, the emerging field of immunometabolism is leading to a refined understanding of how immune cell proliferation and function is governed by glucose homeostasis. Different immune cell types are now known to have unique metabolic signatures that switch in response to a changing environment. T-cell subsets exhibit distinct metabolic profiles which underlie their alternative differentiation and phenotypic functions. Recent evidence shows that the susceptibility of CD4(+) T-cells to HIV infection is intimately linked to their metabolic activity, with many of the metabolic features of HIV-1-infected cells resembling those found in tumor cells. In this review, we discuss the use of miRNA modulation to achieve metabolic reprogramming for cancer therapy and explore the idea that the same approach may serve as an effective mechanism to restrict HIV replication and eliminate infected cells. MDPI 2022-01-29 /pmc/articles/PMC8872267/ /pubmed/35205318 http://dx.doi.org/10.3390/genes13020273 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Gibson, Mark S. Noronha-Estima, Cláudia Gama-Carvalho, Margarida Therapeutic Metabolic Reprograming Using microRNAs: From Cancer to HIV Infection |
title | Therapeutic Metabolic Reprograming Using microRNAs: From Cancer to HIV Infection |
title_full | Therapeutic Metabolic Reprograming Using microRNAs: From Cancer to HIV Infection |
title_fullStr | Therapeutic Metabolic Reprograming Using microRNAs: From Cancer to HIV Infection |
title_full_unstemmed | Therapeutic Metabolic Reprograming Using microRNAs: From Cancer to HIV Infection |
title_short | Therapeutic Metabolic Reprograming Using microRNAs: From Cancer to HIV Infection |
title_sort | therapeutic metabolic reprograming using micrornas: from cancer to hiv infection |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8872267/ https://www.ncbi.nlm.nih.gov/pubmed/35205318 http://dx.doi.org/10.3390/genes13020273 |
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