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The molecular and clinicopathologic characteristics of bilateral breast cancer

In this study, we compared the clinicopathologic characteristics between the bilateral breast cancer (BiBC) and unilateral breast cancer (UBC) and investigated the role of CXC chemokine receptor type 4 (CXCR4) in BiBC. 48 BiBC and 1650 UBC were studied. We found BiBC patients were associated with fa...

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Autores principales: Chen, S. F., Du, C. W., Yang, P., Zhang, H. W., Kwan, M., Zhang, G. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3763252/
https://www.ncbi.nlm.nih.gov/pubmed/24005135
http://dx.doi.org/10.1038/srep02590
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author Chen, S. F.
Du, C. W.
Yang, P.
Zhang, H. W.
Kwan, M.
Zhang, G. J.
author_facet Chen, S. F.
Du, C. W.
Yang, P.
Zhang, H. W.
Kwan, M.
Zhang, G. J.
author_sort Chen, S. F.
collection PubMed
description In this study, we compared the clinicopathologic characteristics between the bilateral breast cancer (BiBC) and unilateral breast cancer (UBC) and investigated the role of CXC chemokine receptor type 4 (CXCR4) in BiBC. 48 BiBC and 1650 UBC were studied. We found BiBC patients were associated with family history of cancer, invasive lobular histology in the first tumor and an advanced nodal status as compared with UBC patients with. Survival analysis indicated that BiBC was not associated with impaired survival. The time interval between the development of first breast cancer and the contralateral cancer did not correlate with the prognosis. Patients with BiBC were more likely to have bone metastasis (P = 0.011) and visceral metastasis (P < 0.001) than those with UBC. However, CXCR4 was not found in any association with poor clinical outcome and increasing visceral metastasis in BiBC patients.
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spelling pubmed-37632522013-09-09 The molecular and clinicopathologic characteristics of bilateral breast cancer Chen, S. F. Du, C. W. Yang, P. Zhang, H. W. Kwan, M. Zhang, G. J. Sci Rep Article In this study, we compared the clinicopathologic characteristics between the bilateral breast cancer (BiBC) and unilateral breast cancer (UBC) and investigated the role of CXC chemokine receptor type 4 (CXCR4) in BiBC. 48 BiBC and 1650 UBC were studied. We found BiBC patients were associated with family history of cancer, invasive lobular histology in the first tumor and an advanced nodal status as compared with UBC patients with. Survival analysis indicated that BiBC was not associated with impaired survival. The time interval between the development of first breast cancer and the contralateral cancer did not correlate with the prognosis. Patients with BiBC were more likely to have bone metastasis (P = 0.011) and visceral metastasis (P < 0.001) than those with UBC. However, CXCR4 was not found in any association with poor clinical outcome and increasing visceral metastasis in BiBC patients. Nature Publishing Group 2013-09-05 /pmc/articles/PMC3763252/ /pubmed/24005135 http://dx.doi.org/10.1038/srep02590 Text en Copyright © 2013, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareALike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Article
Chen, S. F.
Du, C. W.
Yang, P.
Zhang, H. W.
Kwan, M.
Zhang, G. J.
The molecular and clinicopathologic characteristics of bilateral breast cancer
title The molecular and clinicopathologic characteristics of bilateral breast cancer
title_full The molecular and clinicopathologic characteristics of bilateral breast cancer
title_fullStr The molecular and clinicopathologic characteristics of bilateral breast cancer
title_full_unstemmed The molecular and clinicopathologic characteristics of bilateral breast cancer
title_short The molecular and clinicopathologic characteristics of bilateral breast cancer
title_sort molecular and clinicopathologic characteristics of bilateral breast cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3763252/
https://www.ncbi.nlm.nih.gov/pubmed/24005135
http://dx.doi.org/10.1038/srep02590
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