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An Introspective Update on the Influence of miRNAs in Breast Carcinoma and Neuroblastoma Chemoresistance
Chemoresistance to conventional cytotoxic drugs may occur in any type of cancer and this can either be inherent or develop through time. Studies have linked this acquired resistance to the abnormal expression of microRNAs (miRNAs) that normally silence genes. At abnormal levels, miRNAs can either ga...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4273469/ https://www.ncbi.nlm.nih.gov/pubmed/25548681 http://dx.doi.org/10.1155/2014/743050 |
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author | Carta, Alessia Chetcuti, Rachel Ayers, Duncan |
author_facet | Carta, Alessia Chetcuti, Rachel Ayers, Duncan |
author_sort | Carta, Alessia |
collection | PubMed |
description | Chemoresistance to conventional cytotoxic drugs may occur in any type of cancer and this can either be inherent or develop through time. Studies have linked this acquired resistance to the abnormal expression of microRNAs (miRNAs) that normally silence genes. At abnormal levels, miRNAs can either gain ability to silence tumour suppressor genes or else lose ability to silence oncogenes. miRNAs can also affect pathways that are involved in drug metabolism, such as drug efflux pumps, resulting in a resistant phenotype. The scope of this review is to provide an introspective analysis on the specific niches of breast carcinoma and neuroblastoma research. |
format | Online Article Text |
id | pubmed-4273469 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-42734692014-12-29 An Introspective Update on the Influence of miRNAs in Breast Carcinoma and Neuroblastoma Chemoresistance Carta, Alessia Chetcuti, Rachel Ayers, Duncan Genet Res Int Review Article Chemoresistance to conventional cytotoxic drugs may occur in any type of cancer and this can either be inherent or develop through time. Studies have linked this acquired resistance to the abnormal expression of microRNAs (miRNAs) that normally silence genes. At abnormal levels, miRNAs can either gain ability to silence tumour suppressor genes or else lose ability to silence oncogenes. miRNAs can also affect pathways that are involved in drug metabolism, such as drug efflux pumps, resulting in a resistant phenotype. The scope of this review is to provide an introspective analysis on the specific niches of breast carcinoma and neuroblastoma research. Hindawi Publishing Corporation 2014 2014-12-04 /pmc/articles/PMC4273469/ /pubmed/25548681 http://dx.doi.org/10.1155/2014/743050 Text en Copyright © 2014 Alessia Carta et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Carta, Alessia Chetcuti, Rachel Ayers, Duncan An Introspective Update on the Influence of miRNAs in Breast Carcinoma and Neuroblastoma Chemoresistance |
title | An Introspective Update on the Influence of miRNAs in Breast Carcinoma and Neuroblastoma Chemoresistance |
title_full | An Introspective Update on the Influence of miRNAs in Breast Carcinoma and Neuroblastoma Chemoresistance |
title_fullStr | An Introspective Update on the Influence of miRNAs in Breast Carcinoma and Neuroblastoma Chemoresistance |
title_full_unstemmed | An Introspective Update on the Influence of miRNAs in Breast Carcinoma and Neuroblastoma Chemoresistance |
title_short | An Introspective Update on the Influence of miRNAs in Breast Carcinoma and Neuroblastoma Chemoresistance |
title_sort | introspective update on the influence of mirnas in breast carcinoma and neuroblastoma chemoresistance |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4273469/ https://www.ncbi.nlm.nih.gov/pubmed/25548681 http://dx.doi.org/10.1155/2014/743050 |
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