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Understanding the role of NRF2-regulated miRNAs in human malignancies

Nuclear factor (erythroid-derived 2)-like 2 (NRF2) is a key transcription factor that regulates the expression of over a hundred cytoprotective and antioxidant genes that provide cellular protection from reactive oxygen species. Chemotherapy resistance in several cancers has been linked to dysregula...

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Detalles Bibliográficos
Autores principales: Shah, Niraj M, Rushworth, Stuart A, Murray, Megan Y, Bowles, Kristian M, MacEwan, David J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3787145/
https://www.ncbi.nlm.nih.gov/pubmed/24029073
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author Shah, Niraj M
Rushworth, Stuart A
Murray, Megan Y
Bowles, Kristian M
MacEwan, David J
author_facet Shah, Niraj M
Rushworth, Stuart A
Murray, Megan Y
Bowles, Kristian M
MacEwan, David J
author_sort Shah, Niraj M
collection PubMed
description Nuclear factor (erythroid-derived 2)-like 2 (NRF2) is a key transcription factor that regulates the expression of over a hundred cytoprotective and antioxidant genes that provide cellular protection from reactive oxygen species. Chemotherapy resistance in several cancers has been linked to dysregulation of the NRF2 signalling pathway, moreover there is growing evidence that NRF2 may contribute to tumorigenesis. MicroRNA (miRNA) are small non-coding RNA sequences that post-transcriptionally regulate mRNA sequences. In cancer pathogenesis, aberrantly expressed miRNAs can act as either tumor suppressor or oncogenic miRNA. Recent evidence has been described that identifies a number of miRNA that can be regulated by NRF2. This review outlines the importance of NRF2 in regulating miRNA, and the functional role this may have in the tumorigenesis of human malignancies and their chemotherapy resistance.
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spelling pubmed-37871452013-10-01 Understanding the role of NRF2-regulated miRNAs in human malignancies Shah, Niraj M Rushworth, Stuart A Murray, Megan Y Bowles, Kristian M MacEwan, David J Oncotarget Review Nuclear factor (erythroid-derived 2)-like 2 (NRF2) is a key transcription factor that regulates the expression of over a hundred cytoprotective and antioxidant genes that provide cellular protection from reactive oxygen species. Chemotherapy resistance in several cancers has been linked to dysregulation of the NRF2 signalling pathway, moreover there is growing evidence that NRF2 may contribute to tumorigenesis. MicroRNA (miRNA) are small non-coding RNA sequences that post-transcriptionally regulate mRNA sequences. In cancer pathogenesis, aberrantly expressed miRNAs can act as either tumor suppressor or oncogenic miRNA. Recent evidence has been described that identifies a number of miRNA that can be regulated by NRF2. This review outlines the importance of NRF2 in regulating miRNA, and the functional role this may have in the tumorigenesis of human malignancies and their chemotherapy resistance. Impact Journals LLC 2013-08-08 /pmc/articles/PMC3787145/ /pubmed/24029073 Text en Copyright: © 2013 Shah et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
spellingShingle Review
Shah, Niraj M
Rushworth, Stuart A
Murray, Megan Y
Bowles, Kristian M
MacEwan, David J
Understanding the role of NRF2-regulated miRNAs in human malignancies
title Understanding the role of NRF2-regulated miRNAs in human malignancies
title_full Understanding the role of NRF2-regulated miRNAs in human malignancies
title_fullStr Understanding the role of NRF2-regulated miRNAs in human malignancies
title_full_unstemmed Understanding the role of NRF2-regulated miRNAs in human malignancies
title_short Understanding the role of NRF2-regulated miRNAs in human malignancies
title_sort understanding the role of nrf2-regulated mirnas in human malignancies
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3787145/
https://www.ncbi.nlm.nih.gov/pubmed/24029073
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