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The prognostic significance of topoisomerase II alpha protein in early stage luminal breast cancer

BACKGROUND: Topoisomerase II alpha (TOP2A) protein has been shown to be a proliferation marker associated with tumor grade and Ki67 index. The prognostic effect of TOP2A seems different among different subtypes of breast cancer. The current study evaluated the prognostic impact of TOP2A protein on l...

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Autores principales: An, Xin, Xu, Fei, Luo, Rongzhen, Zheng, Qiufan, Lu, Jiabin, Yang, Yanhua, Qin, Tao, Yuan, Zhongyu, Shi, Yanxia, Jiang, Wenqi, Wang, Shusen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870251/
https://www.ncbi.nlm.nih.gov/pubmed/29587760
http://dx.doi.org/10.1186/s12885-018-4170-7
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author An, Xin
Xu, Fei
Luo, Rongzhen
Zheng, Qiufan
Lu, Jiabin
Yang, Yanhua
Qin, Tao
Yuan, Zhongyu
Shi, Yanxia
Jiang, Wenqi
Wang, Shusen
author_facet An, Xin
Xu, Fei
Luo, Rongzhen
Zheng, Qiufan
Lu, Jiabin
Yang, Yanhua
Qin, Tao
Yuan, Zhongyu
Shi, Yanxia
Jiang, Wenqi
Wang, Shusen
author_sort An, Xin
collection PubMed
description BACKGROUND: Topoisomerase II alpha (TOP2A) protein has been shown to be a proliferation marker associated with tumor grade and Ki67 index. The prognostic effect of TOP2A seems different among different subtypes of breast cancer. The current study evaluated the prognostic impact of TOP2A protein on luminal breast cancer. METHOD: Altogether 434 stage I-II luminal breast cancer patients who underwent curative surgery in Sun Yat-Sen University Cancer Center between 2007 and 2009 were enrolled. TOP2A protein expression was assessed by immunohistochemistry. Clinical and pathological data were retrospectively collected. RESULT: With a cut-off value of 30%, 127 (29.3%) patients were classified as TOP2A overexpression. TOP2A overexpression was associated with a higher tumor grade and Ki67 index. Patients with TOP2A high expression showed a significantly higher rate of distant metastasis and shorter distant metastasis free survival (DMFS) compared with patients with low TOP2A expression. The prognostic influence of TOP2A expression was more significant in years 5–8 after diagnosis, and more pronounced in stage II patients, luminal B disease, and patients treated with adjuvant endocrine therapy alone. Multivariate survival analysis revealed TOP2A overexpression was an independent fact for worse DMFS. CONCLUSION: TOP2A protein showed a time dependent influence on prognosis in stage I-II luminal breast cancer, suggesting it might be a potential predictor of late recurrence for this group of patients.
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spelling pubmed-58702512018-03-29 The prognostic significance of topoisomerase II alpha protein in early stage luminal breast cancer An, Xin Xu, Fei Luo, Rongzhen Zheng, Qiufan Lu, Jiabin Yang, Yanhua Qin, Tao Yuan, Zhongyu Shi, Yanxia Jiang, Wenqi Wang, Shusen BMC Cancer Research Article BACKGROUND: Topoisomerase II alpha (TOP2A) protein has been shown to be a proliferation marker associated with tumor grade and Ki67 index. The prognostic effect of TOP2A seems different among different subtypes of breast cancer. The current study evaluated the prognostic impact of TOP2A protein on luminal breast cancer. METHOD: Altogether 434 stage I-II luminal breast cancer patients who underwent curative surgery in Sun Yat-Sen University Cancer Center between 2007 and 2009 were enrolled. TOP2A protein expression was assessed by immunohistochemistry. Clinical and pathological data were retrospectively collected. RESULT: With a cut-off value of 30%, 127 (29.3%) patients were classified as TOP2A overexpression. TOP2A overexpression was associated with a higher tumor grade and Ki67 index. Patients with TOP2A high expression showed a significantly higher rate of distant metastasis and shorter distant metastasis free survival (DMFS) compared with patients with low TOP2A expression. The prognostic influence of TOP2A expression was more significant in years 5–8 after diagnosis, and more pronounced in stage II patients, luminal B disease, and patients treated with adjuvant endocrine therapy alone. Multivariate survival analysis revealed TOP2A overexpression was an independent fact for worse DMFS. CONCLUSION: TOP2A protein showed a time dependent influence on prognosis in stage I-II luminal breast cancer, suggesting it might be a potential predictor of late recurrence for this group of patients. BioMed Central 2018-03-27 /pmc/articles/PMC5870251/ /pubmed/29587760 http://dx.doi.org/10.1186/s12885-018-4170-7 Text en © The Author(s). 2018 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
An, Xin
Xu, Fei
Luo, Rongzhen
Zheng, Qiufan
Lu, Jiabin
Yang, Yanhua
Qin, Tao
Yuan, Zhongyu
Shi, Yanxia
Jiang, Wenqi
Wang, Shusen
The prognostic significance of topoisomerase II alpha protein in early stage luminal breast cancer
title The prognostic significance of topoisomerase II alpha protein in early stage luminal breast cancer
title_full The prognostic significance of topoisomerase II alpha protein in early stage luminal breast cancer
title_fullStr The prognostic significance of topoisomerase II alpha protein in early stage luminal breast cancer
title_full_unstemmed The prognostic significance of topoisomerase II alpha protein in early stage luminal breast cancer
title_short The prognostic significance of topoisomerase II alpha protein in early stage luminal breast cancer
title_sort prognostic significance of topoisomerase ii alpha protein in early stage luminal breast cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870251/
https://www.ncbi.nlm.nih.gov/pubmed/29587760
http://dx.doi.org/10.1186/s12885-018-4170-7
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