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Identification of therapeutic targets and prognostic biomarkers from the hnRNP family in invasive breast carcinoma
Heterogeneous nuclear ribonucleoproteins (hnRNPs) are RNA-binding proteins that are reported to play a crucial role in the pathogenic process of multiple malignancies. However, their expression patterns, clinical application significance and prognostic values in invasive breast carcinoma (BRCA) rema...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7906176/ https://www.ncbi.nlm.nih.gov/pubmed/33495416 http://dx.doi.org/10.18632/aging.202411 |
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author | Zhou, Jiawei Guo, Yugang Huo, Zheng Xing, Yuxin Fang, Jintao Ma, Guohui Han, Qinghui Wang, Mengzhen Xu, Qian |
author_facet | Zhou, Jiawei Guo, Yugang Huo, Zheng Xing, Yuxin Fang, Jintao Ma, Guohui Han, Qinghui Wang, Mengzhen Xu, Qian |
author_sort | Zhou, Jiawei |
collection | PubMed |
description | Heterogeneous nuclear ribonucleoproteins (hnRNPs) are RNA-binding proteins that are reported to play a crucial role in the pathogenic process of multiple malignancies. However, their expression patterns, clinical application significance and prognostic values in invasive breast carcinoma (BRCA) remain unknown. In this study, we investigated hnRNP family members in BRCA using accumulated data from Oncomine 4.5, UALCAN Web portal and other available databases. We explored the expression and prognostic value level of hnRNPs in BRCA. We further analyzed their association with the clinicopathological features of BRCA patients. Subsequently, we calculated the alteration frequency of hnRNPs, constructed the interaction network of hnRNPs, and examined the potential coexpression genes of hnRNPs, revealing that HNRNPU and SYNCRIP are the core molecular genes requiring further investigation for BRCA. We validated the immunohistochemistry (IHC) pattern to simulate clinical applications based on pathology. Cell function experiments conducted in vitro indicated that HNRNPU can promote epithelial-mesenchymal transition, functionally stimulating the invasion capacity and inhibiting the viability of invasive BRCA cells. In summary, our systematic analysis demonstrated that HNRNPU was the key molecule that played a fundamental role in BRCA metastasis, which may facilitate the development of new diagnostic and prognostic markers for the analysis of BRCA progression. |
format | Online Article Text |
id | pubmed-7906176 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-79061762021-03-04 Identification of therapeutic targets and prognostic biomarkers from the hnRNP family in invasive breast carcinoma Zhou, Jiawei Guo, Yugang Huo, Zheng Xing, Yuxin Fang, Jintao Ma, Guohui Han, Qinghui Wang, Mengzhen Xu, Qian Aging (Albany NY) Research Paper Heterogeneous nuclear ribonucleoproteins (hnRNPs) are RNA-binding proteins that are reported to play a crucial role in the pathogenic process of multiple malignancies. However, their expression patterns, clinical application significance and prognostic values in invasive breast carcinoma (BRCA) remain unknown. In this study, we investigated hnRNP family members in BRCA using accumulated data from Oncomine 4.5, UALCAN Web portal and other available databases. We explored the expression and prognostic value level of hnRNPs in BRCA. We further analyzed their association with the clinicopathological features of BRCA patients. Subsequently, we calculated the alteration frequency of hnRNPs, constructed the interaction network of hnRNPs, and examined the potential coexpression genes of hnRNPs, revealing that HNRNPU and SYNCRIP are the core molecular genes requiring further investigation for BRCA. We validated the immunohistochemistry (IHC) pattern to simulate clinical applications based on pathology. Cell function experiments conducted in vitro indicated that HNRNPU can promote epithelial-mesenchymal transition, functionally stimulating the invasion capacity and inhibiting the viability of invasive BRCA cells. In summary, our systematic analysis demonstrated that HNRNPU was the key molecule that played a fundamental role in BRCA metastasis, which may facilitate the development of new diagnostic and prognostic markers for the analysis of BRCA progression. Impact Journals 2021-01-20 /pmc/articles/PMC7906176/ /pubmed/33495416 http://dx.doi.org/10.18632/aging.202411 Text en Copyright: © 2021 Zhou et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Zhou, Jiawei Guo, Yugang Huo, Zheng Xing, Yuxin Fang, Jintao Ma, Guohui Han, Qinghui Wang, Mengzhen Xu, Qian Identification of therapeutic targets and prognostic biomarkers from the hnRNP family in invasive breast carcinoma |
title | Identification of therapeutic targets and prognostic biomarkers from the hnRNP family in invasive breast carcinoma |
title_full | Identification of therapeutic targets and prognostic biomarkers from the hnRNP family in invasive breast carcinoma |
title_fullStr | Identification of therapeutic targets and prognostic biomarkers from the hnRNP family in invasive breast carcinoma |
title_full_unstemmed | Identification of therapeutic targets and prognostic biomarkers from the hnRNP family in invasive breast carcinoma |
title_short | Identification of therapeutic targets and prognostic biomarkers from the hnRNP family in invasive breast carcinoma |
title_sort | identification of therapeutic targets and prognostic biomarkers from the hnrnp family in invasive breast carcinoma |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7906176/ https://www.ncbi.nlm.nih.gov/pubmed/33495416 http://dx.doi.org/10.18632/aging.202411 |
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