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The long-term prognostic and predictive capacity of cyclin D1 gene amplification in 2305 breast tumours

BACKGROUND: Use of cyclin D1 (CCND1) gene amplification as a breast cancer biomarker has been hampered by conflicting assessments of the relationship between cyclin D1 protein levels and patient survival. Here, we aimed to clarify its prognostic and treatment predictive potential through comprehensi...

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Autores principales: Lundberg, Arian, Lindström, Linda S., Li, Jingmei, Harrell, J. Chuck, Darai-Ramqvist, Eva, Sifakis, Emmanouil G., Foukakis, Theodoros, Perou, Charles M., Czene, Kamila, Bergh, Jonas, Tobin, Nicholas P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6394106/
https://www.ncbi.nlm.nih.gov/pubmed/30819233
http://dx.doi.org/10.1186/s13058-019-1121-4
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author Lundberg, Arian
Lindström, Linda S.
Li, Jingmei
Harrell, J. Chuck
Darai-Ramqvist, Eva
Sifakis, Emmanouil G.
Foukakis, Theodoros
Perou, Charles M.
Czene, Kamila
Bergh, Jonas
Tobin, Nicholas P.
author_facet Lundberg, Arian
Lindström, Linda S.
Li, Jingmei
Harrell, J. Chuck
Darai-Ramqvist, Eva
Sifakis, Emmanouil G.
Foukakis, Theodoros
Perou, Charles M.
Czene, Kamila
Bergh, Jonas
Tobin, Nicholas P.
author_sort Lundberg, Arian
collection PubMed
description BACKGROUND: Use of cyclin D1 (CCND1) gene amplification as a breast cancer biomarker has been hampered by conflicting assessments of the relationship between cyclin D1 protein levels and patient survival. Here, we aimed to clarify its prognostic and treatment predictive potential through comprehensive long-term survival analyses. METHODS: CCND1 amplification was assessed using SNP arrays from two cohorts of 1965 and 340 patients with matching gene expression array and clinical follow-up data of over 15 years. Kaplan-Meier and multivariable Cox regression analyses were used to determine survival differences between CCND1 amplified vs. non-amplified tumours in clinically relevant patient sets, within PAM50 subtypes and within treatment-specific subgroups. Boxplots and differential gene expression analyses were performed to assess differences between amplified vs. non-amplified tumours within PAM50 subtypes. RESULTS: When combining both cohorts, worse survival was found for patients with CCND1-amplified tumours in luminal A (HR = 1.68; 95% CI, 1.15–2.46), luminal B (1.37; 1.01–1.86) and ER+/LN−/HER2− (1.66; 1.14–2.41) subgroups. In gene expression analysis, CCND1-amplified luminal A tumours showed increased proliferation (P < 0.001) and decreased progesterone (P = 0.002) levels along with a large overlap in differentially expressed genes when comparing luminal A and B-amplified vs. non-amplified tumours. CONCLUSIONS: Our results indicate that CCND1 amplification is associated with worse 15-year survival in ER+/LN−/HER2−, luminal A and luminal B patients. Moreover, luminal A CCND1-amplified tumours display gene expression changes consistent with a more aggressive phenotype. These novel findings highlight the potential of CCND1 to identify patients that could benefit from long-term treatment strategies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13058-019-1121-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-63941062019-03-11 The long-term prognostic and predictive capacity of cyclin D1 gene amplification in 2305 breast tumours Lundberg, Arian Lindström, Linda S. Li, Jingmei Harrell, J. Chuck Darai-Ramqvist, Eva Sifakis, Emmanouil G. Foukakis, Theodoros Perou, Charles M. Czene, Kamila Bergh, Jonas Tobin, Nicholas P. Breast Cancer Res Research Article BACKGROUND: Use of cyclin D1 (CCND1) gene amplification as a breast cancer biomarker has been hampered by conflicting assessments of the relationship between cyclin D1 protein levels and patient survival. Here, we aimed to clarify its prognostic and treatment predictive potential through comprehensive long-term survival analyses. METHODS: CCND1 amplification was assessed using SNP arrays from two cohorts of 1965 and 340 patients with matching gene expression array and clinical follow-up data of over 15 years. Kaplan-Meier and multivariable Cox regression analyses were used to determine survival differences between CCND1 amplified vs. non-amplified tumours in clinically relevant patient sets, within PAM50 subtypes and within treatment-specific subgroups. Boxplots and differential gene expression analyses were performed to assess differences between amplified vs. non-amplified tumours within PAM50 subtypes. RESULTS: When combining both cohorts, worse survival was found for patients with CCND1-amplified tumours in luminal A (HR = 1.68; 95% CI, 1.15–2.46), luminal B (1.37; 1.01–1.86) and ER+/LN−/HER2− (1.66; 1.14–2.41) subgroups. In gene expression analysis, CCND1-amplified luminal A tumours showed increased proliferation (P < 0.001) and decreased progesterone (P = 0.002) levels along with a large overlap in differentially expressed genes when comparing luminal A and B-amplified vs. non-amplified tumours. CONCLUSIONS: Our results indicate that CCND1 amplification is associated with worse 15-year survival in ER+/LN−/HER2−, luminal A and luminal B patients. Moreover, luminal A CCND1-amplified tumours display gene expression changes consistent with a more aggressive phenotype. These novel findings highlight the potential of CCND1 to identify patients that could benefit from long-term treatment strategies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13058-019-1121-4) contains supplementary material, which is available to authorized users. BioMed Central 2019-02-28 2019 /pmc/articles/PMC6394106/ /pubmed/30819233 http://dx.doi.org/10.1186/s13058-019-1121-4 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Lundberg, Arian
Lindström, Linda S.
Li, Jingmei
Harrell, J. Chuck
Darai-Ramqvist, Eva
Sifakis, Emmanouil G.
Foukakis, Theodoros
Perou, Charles M.
Czene, Kamila
Bergh, Jonas
Tobin, Nicholas P.
The long-term prognostic and predictive capacity of cyclin D1 gene amplification in 2305 breast tumours
title The long-term prognostic and predictive capacity of cyclin D1 gene amplification in 2305 breast tumours
title_full The long-term prognostic and predictive capacity of cyclin D1 gene amplification in 2305 breast tumours
title_fullStr The long-term prognostic and predictive capacity of cyclin D1 gene amplification in 2305 breast tumours
title_full_unstemmed The long-term prognostic and predictive capacity of cyclin D1 gene amplification in 2305 breast tumours
title_short The long-term prognostic and predictive capacity of cyclin D1 gene amplification in 2305 breast tumours
title_sort long-term prognostic and predictive capacity of cyclin d1 gene amplification in 2305 breast tumours
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6394106/
https://www.ncbi.nlm.nih.gov/pubmed/30819233
http://dx.doi.org/10.1186/s13058-019-1121-4
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