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Evaluation of the role of KPNA2 mutations in breast cancer prognosis using bioinformatics datasets
Breast cancer, comprising of several sub-phenotypes, is a leading cause of female cancer-related mortality in the UK and accounts for 15% of all cancer cases. Chemoresistant sub phenotypes of breast cancer remain a particular challenge. However, the rapidly-growing availability of clinical datasets,...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9364282/ https://www.ncbi.nlm.nih.gov/pubmed/35948941 http://dx.doi.org/10.1186/s12885-022-09969-4 |
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author | Alnoumas, Layla van den Driest, Lisa Apczynski, Zoe Lannigan, Alison Johnson, Caroline H. Rattray, Nicholas J. W. Rattray, Zahra |
author_facet | Alnoumas, Layla van den Driest, Lisa Apczynski, Zoe Lannigan, Alison Johnson, Caroline H. Rattray, Nicholas J. W. Rattray, Zahra |
author_sort | Alnoumas, Layla |
collection | PubMed |
description | Breast cancer, comprising of several sub-phenotypes, is a leading cause of female cancer-related mortality in the UK and accounts for 15% of all cancer cases. Chemoresistant sub phenotypes of breast cancer remain a particular challenge. However, the rapidly-growing availability of clinical datasets, presents the scope to underpin a data-driven precision medicine-based approach exploring new targets for diagnostic and therapeutic interventions. We report the application of a bioinformatics-based approach probing the expression and prognostic role of Karyopherin-2 alpha (KPNA2) in breast cancer prognosis. Aberrant KPNA2 overexpression is directly correlated with aggressive tumour phenotypes and poor patient survival outcomes. We examined the existing clinical data available on a range of commonly occurring mutations of KPNA2 and their correlation with patient survival. Our analysis of clinical gene expression datasets show that KPNA2 is frequently amplified in breast cancer, with differences in expression levels observed as a function of patient age and clinicopathologic parameters. We also found that aberrant KPNA2 overexpression is directly correlated with poor patient prognosis, warranting further investigation of KPNA2 as an actionable target for patient stratification or the design of novel chemotherapy agents. In the era of big data, the wealth of datasets available in the public domain can be used to underpin proof of concept studies evaluating the biomolecular pathways implicated in chemotherapy resistance in breast cancer. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-022-09969-4. |
format | Online Article Text |
id | pubmed-9364282 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-93642822022-08-10 Evaluation of the role of KPNA2 mutations in breast cancer prognosis using bioinformatics datasets Alnoumas, Layla van den Driest, Lisa Apczynski, Zoe Lannigan, Alison Johnson, Caroline H. Rattray, Nicholas J. W. Rattray, Zahra BMC Cancer Research Breast cancer, comprising of several sub-phenotypes, is a leading cause of female cancer-related mortality in the UK and accounts for 15% of all cancer cases. Chemoresistant sub phenotypes of breast cancer remain a particular challenge. However, the rapidly-growing availability of clinical datasets, presents the scope to underpin a data-driven precision medicine-based approach exploring new targets for diagnostic and therapeutic interventions. We report the application of a bioinformatics-based approach probing the expression and prognostic role of Karyopherin-2 alpha (KPNA2) in breast cancer prognosis. Aberrant KPNA2 overexpression is directly correlated with aggressive tumour phenotypes and poor patient survival outcomes. We examined the existing clinical data available on a range of commonly occurring mutations of KPNA2 and their correlation with patient survival. Our analysis of clinical gene expression datasets show that KPNA2 is frequently amplified in breast cancer, with differences in expression levels observed as a function of patient age and clinicopathologic parameters. We also found that aberrant KPNA2 overexpression is directly correlated with poor patient prognosis, warranting further investigation of KPNA2 as an actionable target for patient stratification or the design of novel chemotherapy agents. In the era of big data, the wealth of datasets available in the public domain can be used to underpin proof of concept studies evaluating the biomolecular pathways implicated in chemotherapy resistance in breast cancer. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-022-09969-4. BioMed Central 2022-08-10 /pmc/articles/PMC9364282/ /pubmed/35948941 http://dx.doi.org/10.1186/s12885-022-09969-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Alnoumas, Layla van den Driest, Lisa Apczynski, Zoe Lannigan, Alison Johnson, Caroline H. Rattray, Nicholas J. W. Rattray, Zahra Evaluation of the role of KPNA2 mutations in breast cancer prognosis using bioinformatics datasets |
title | Evaluation of the role of KPNA2 mutations in breast cancer prognosis using bioinformatics datasets |
title_full | Evaluation of the role of KPNA2 mutations in breast cancer prognosis using bioinformatics datasets |
title_fullStr | Evaluation of the role of KPNA2 mutations in breast cancer prognosis using bioinformatics datasets |
title_full_unstemmed | Evaluation of the role of KPNA2 mutations in breast cancer prognosis using bioinformatics datasets |
title_short | Evaluation of the role of KPNA2 mutations in breast cancer prognosis using bioinformatics datasets |
title_sort | evaluation of the role of kpna2 mutations in breast cancer prognosis using bioinformatics datasets |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9364282/ https://www.ncbi.nlm.nih.gov/pubmed/35948941 http://dx.doi.org/10.1186/s12885-022-09969-4 |
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