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The effect of smoking on biological change of recurrent breast cancer

BACKGROUND: The selection of treatment for a patient with breast cancer largely relies on the cancer subtype. However, this process is complicated by changes in tumor biology at relapse. Smoking has been identified as a risk factor for breast cancer. The direct effect of a tobacco component delivere...

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Autores principales: Takada, Koji, Kashiwagi, Shinichiro, Asano, Yuka, Goto, Wataru, Kouhashi, Rika, Yabumoto, Akimichi, Morisaki, Tamami, Fujita, Hisakazu, Shibutani, Masatsune, Takashima, Tsutomu, Hirakawa, Kosei, Ohira, Masaichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7132886/
https://www.ncbi.nlm.nih.gov/pubmed/32248830
http://dx.doi.org/10.1186/s12967-020-02307-x
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author Takada, Koji
Kashiwagi, Shinichiro
Asano, Yuka
Goto, Wataru
Kouhashi, Rika
Yabumoto, Akimichi
Morisaki, Tamami
Fujita, Hisakazu
Shibutani, Masatsune
Takashima, Tsutomu
Hirakawa, Kosei
Ohira, Masaichi
author_facet Takada, Koji
Kashiwagi, Shinichiro
Asano, Yuka
Goto, Wataru
Kouhashi, Rika
Yabumoto, Akimichi
Morisaki, Tamami
Fujita, Hisakazu
Shibutani, Masatsune
Takashima, Tsutomu
Hirakawa, Kosei
Ohira, Masaichi
author_sort Takada, Koji
collection PubMed
description BACKGROUND: The selection of treatment for a patient with breast cancer largely relies on the cancer subtype. However, this process is complicated by changes in tumor biology at relapse. Smoking has been identified as a risk factor for breast cancer. The direct effect of a tobacco component delivered via blood circulation on the mammary gland tissue and subsequent DNA damage have been proposed to explain the association between cigarette smoking and breast cancer carcinogenesis. This postulation is supported by both tissue culture and animal studies demonstrating that the associated DNA damage further alters breast cancer cells, as indicated by an increased proliferative capacity and malignant transformation. In this study, we aimed to explore the relationship between changes in Estrogen receptor (ER), progesterone receptor (PgR), and human epidermal growth factor receptor 2 (HER2) each receptor at recurrence, and smoking and the prognosis after recurrence. METHODS: This retrospective study included 989 patients with primary breast cancer who developed relapse after surgery and 50 patients who underwent regenerative biopsy or surgery from December 2007 to March 2018. ER, PgR, and HER2 expression in the primary and recurrent lesions was evaluated using immunohistochemistry, and the correlations of these expression patterns with smoking history (pack-years) were examined. RESULTS: When ER was evaluated in recurrent tumors, negative and positive conversions were recognized in 3 (6.0%) and 1 patient (2.0%), respectively. When PgR was evaluated, negative conversion was recognized in 15 patients (30.0%). When HER2 was evaluated, positive conversion was recognized in 6 patients (12.0%). Consequently, we observed a change in the intrinsic subtype in in 5 patients with recurrent tumors (10.0%). Although most clinical factors were not correlated with smoking, a positive conversion of HER2 in recurrence was significantly more frequent among smokers than among non-smokers (p = 0.024). CONCLUSIONS: Biological changes during breast cancer recurrence should be given careful clinical consideration because they affect treatment after recurrence. Our results suggest that smoking may induce increased HER2 expression in recurrent breast tumors.
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spelling pubmed-71328862020-04-11 The effect of smoking on biological change of recurrent breast cancer Takada, Koji Kashiwagi, Shinichiro Asano, Yuka Goto, Wataru Kouhashi, Rika Yabumoto, Akimichi Morisaki, Tamami Fujita, Hisakazu Shibutani, Masatsune Takashima, Tsutomu Hirakawa, Kosei Ohira, Masaichi J Transl Med Research BACKGROUND: The selection of treatment for a patient with breast cancer largely relies on the cancer subtype. However, this process is complicated by changes in tumor biology at relapse. Smoking has been identified as a risk factor for breast cancer. The direct effect of a tobacco component delivered via blood circulation on the mammary gland tissue and subsequent DNA damage have been proposed to explain the association between cigarette smoking and breast cancer carcinogenesis. This postulation is supported by both tissue culture and animal studies demonstrating that the associated DNA damage further alters breast cancer cells, as indicated by an increased proliferative capacity and malignant transformation. In this study, we aimed to explore the relationship between changes in Estrogen receptor (ER), progesterone receptor (PgR), and human epidermal growth factor receptor 2 (HER2) each receptor at recurrence, and smoking and the prognosis after recurrence. METHODS: This retrospective study included 989 patients with primary breast cancer who developed relapse after surgery and 50 patients who underwent regenerative biopsy or surgery from December 2007 to March 2018. ER, PgR, and HER2 expression in the primary and recurrent lesions was evaluated using immunohistochemistry, and the correlations of these expression patterns with smoking history (pack-years) were examined. RESULTS: When ER was evaluated in recurrent tumors, negative and positive conversions were recognized in 3 (6.0%) and 1 patient (2.0%), respectively. When PgR was evaluated, negative conversion was recognized in 15 patients (30.0%). When HER2 was evaluated, positive conversion was recognized in 6 patients (12.0%). Consequently, we observed a change in the intrinsic subtype in in 5 patients with recurrent tumors (10.0%). Although most clinical factors were not correlated with smoking, a positive conversion of HER2 in recurrence was significantly more frequent among smokers than among non-smokers (p = 0.024). CONCLUSIONS: Biological changes during breast cancer recurrence should be given careful clinical consideration because they affect treatment after recurrence. Our results suggest that smoking may induce increased HER2 expression in recurrent breast tumors. BioMed Central 2020-04-05 /pmc/articles/PMC7132886/ /pubmed/32248830 http://dx.doi.org/10.1186/s12967-020-02307-x Text en © The Author(s) 2020 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/. 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 in a credit line to the data.
spellingShingle Research
Takada, Koji
Kashiwagi, Shinichiro
Asano, Yuka
Goto, Wataru
Kouhashi, Rika
Yabumoto, Akimichi
Morisaki, Tamami
Fujita, Hisakazu
Shibutani, Masatsune
Takashima, Tsutomu
Hirakawa, Kosei
Ohira, Masaichi
The effect of smoking on biological change of recurrent breast cancer
title The effect of smoking on biological change of recurrent breast cancer
title_full The effect of smoking on biological change of recurrent breast cancer
title_fullStr The effect of smoking on biological change of recurrent breast cancer
title_full_unstemmed The effect of smoking on biological change of recurrent breast cancer
title_short The effect of smoking on biological change of recurrent breast cancer
title_sort effect of smoking on biological change of recurrent breast cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7132886/
https://www.ncbi.nlm.nih.gov/pubmed/32248830
http://dx.doi.org/10.1186/s12967-020-02307-x
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