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Analysis of Cyclin D1 in Breast Cancer: A Call to Arms
The oncogenic capabilities of the cell cycle protein cyclin D1 have long been established in a breast cancer setting. The CCND1 gene is amplified in up to 15 % of breast tumors, with overexpression of its corresponding protein found in up to 50 % of cases. While gene amplification is consistently as...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Current Science Inc.
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3410026/ https://www.ncbi.nlm.nih.gov/pubmed/22924091 http://dx.doi.org/10.1007/s12609-012-0083-7 |
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author | Tobin, Nicholas P. Bergh, Jonas |
author_facet | Tobin, Nicholas P. Bergh, Jonas |
author_sort | Tobin, Nicholas P. |
collection | PubMed |
description | The oncogenic capabilities of the cell cycle protein cyclin D1 have long been established in a breast cancer setting. The CCND1 gene is amplified in up to 15 % of breast tumors, with overexpression of its corresponding protein found in up to 50 % of cases. While gene amplification is consistently associated with reduced patient survival times and treatment resistance, repeated attempts to clarify the prognostic and predictive impact of the cyclin D1 protein in breast cancer have yielded contrasting results. Here, we recommend that any examination of cyclin D1 in a patient cohort should begin by determining CCND1 copy number, with subsequent removal and separate analysis of amplified cases. Next, the remaining tumors should be examined for cyclin D1 protein expression in the context of well-defined breast cancer subgroups. Only in this manner can the true clinical value of cyclin D1 be fully elucidated. |
format | Online Article Text |
id | pubmed-3410026 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Current Science Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-34100262012-08-24 Analysis of Cyclin D1 in Breast Cancer: A Call to Arms Tobin, Nicholas P. Bergh, Jonas Curr Breast Cancer Rep Invited Commentary The oncogenic capabilities of the cell cycle protein cyclin D1 have long been established in a breast cancer setting. The CCND1 gene is amplified in up to 15 % of breast tumors, with overexpression of its corresponding protein found in up to 50 % of cases. While gene amplification is consistently associated with reduced patient survival times and treatment resistance, repeated attempts to clarify the prognostic and predictive impact of the cyclin D1 protein in breast cancer have yielded contrasting results. Here, we recommend that any examination of cyclin D1 in a patient cohort should begin by determining CCND1 copy number, with subsequent removal and separate analysis of amplified cases. Next, the remaining tumors should be examined for cyclin D1 protein expression in the context of well-defined breast cancer subgroups. Only in this manner can the true clinical value of cyclin D1 be fully elucidated. Current Science Inc. 2012-06-22 2012 /pmc/articles/PMC3410026/ /pubmed/22924091 http://dx.doi.org/10.1007/s12609-012-0083-7 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Invited Commentary Tobin, Nicholas P. Bergh, Jonas Analysis of Cyclin D1 in Breast Cancer: A Call to Arms |
title | Analysis of Cyclin D1 in Breast Cancer: A Call to Arms |
title_full | Analysis of Cyclin D1 in Breast Cancer: A Call to Arms |
title_fullStr | Analysis of Cyclin D1 in Breast Cancer: A Call to Arms |
title_full_unstemmed | Analysis of Cyclin D1 in Breast Cancer: A Call to Arms |
title_short | Analysis of Cyclin D1 in Breast Cancer: A Call to Arms |
title_sort | analysis of cyclin d1 in breast cancer: a call to arms |
topic | Invited Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3410026/ https://www.ncbi.nlm.nih.gov/pubmed/22924091 http://dx.doi.org/10.1007/s12609-012-0083-7 |
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