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Identification of new miRNA biomarkers associated with HER2-positive breast cancers
Human epidermal growth factor receptor 2 (HER2) is overexpressed/amplified in ∼30% breast cancers which are associated with poor prognosis. microRNAs are small non-coding RNA which play an important role in many physiological conditions including cancer. Here we screened and identified many miRNAs w...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4675790/ https://www.ncbi.nlm.nih.gov/pubmed/26697527 |
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author | Tashkandi, Hossam Shah, Nirav Patel, Yogin Chen, Hexin |
author_facet | Tashkandi, Hossam Shah, Nirav Patel, Yogin Chen, Hexin |
author_sort | Tashkandi, Hossam |
collection | PubMed |
description | Human epidermal growth factor receptor 2 (HER2) is overexpressed/amplified in ∼30% breast cancers which are associated with poor prognosis. microRNAs are small non-coding RNA which play an important role in many physiological conditions including cancer. Here we screened and identified many miRNAs which are dysregulated by HER2 overexpression. In line with our quantitative PCR analysis data, in silico analysis of microRNA expression profiles of 1302 breast tumors revealed that miR-146a-5p is up-regulated and miR-181d and miR-195-5p are down-regulated in HER2-positive tumors. Furthermore, the expression levels of these microRNAs can significantly predict patient survival and thus potentially serve as new prognostic markers for HER2-positive breast cancer. |
format | Online Article Text |
id | pubmed-4675790 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-46757902015-12-22 Identification of new miRNA biomarkers associated with HER2-positive breast cancers Tashkandi, Hossam Shah, Nirav Patel, Yogin Chen, Hexin Oncoscience Research Paper Human epidermal growth factor receptor 2 (HER2) is overexpressed/amplified in ∼30% breast cancers which are associated with poor prognosis. microRNAs are small non-coding RNA which play an important role in many physiological conditions including cancer. Here we screened and identified many miRNAs which are dysregulated by HER2 overexpression. In line with our quantitative PCR analysis data, in silico analysis of microRNA expression profiles of 1302 breast tumors revealed that miR-146a-5p is up-regulated and miR-181d and miR-195-5p are down-regulated in HER2-positive tumors. Furthermore, the expression levels of these microRNAs can significantly predict patient survival and thus potentially serve as new prognostic markers for HER2-positive breast cancer. Impact Journals LLC 2015-12-02 /pmc/articles/PMC4675790/ /pubmed/26697527 Text en Copyright: © 2015 Tashkandi 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 | Research Paper Tashkandi, Hossam Shah, Nirav Patel, Yogin Chen, Hexin Identification of new miRNA biomarkers associated with HER2-positive breast cancers |
title | Identification of new miRNA biomarkers associated with HER2-positive breast cancers |
title_full | Identification of new miRNA biomarkers associated with HER2-positive breast cancers |
title_fullStr | Identification of new miRNA biomarkers associated with HER2-positive breast cancers |
title_full_unstemmed | Identification of new miRNA biomarkers associated with HER2-positive breast cancers |
title_short | Identification of new miRNA biomarkers associated with HER2-positive breast cancers |
title_sort | identification of new mirna biomarkers associated with her2-positive breast cancers |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4675790/ https://www.ncbi.nlm.nih.gov/pubmed/26697527 |
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