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Published in: International Journal of Clinical Oncology 3/2014

01-06-2014 | Original Article

Influence of body mass index on clinicopathological factors including estrogen receptor, progesterone receptor, and Ki67 expression levels in breast cancers

Authors: Ayako Yanai, Yoshimasa Miyagawa, Keiko Murase, Michiko Imamura, Tomoko Yagi, Shigetoshi Ichii, Yuichi Takatsuka, Takashi Ito, Seiichi Hirota, Mitsunori Sasa, Toyomasa Katagiri, Yasuo Miyoshi

Published in: International Journal of Clinical Oncology | Issue 3/2014

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Abstract

Background

High body mass index (BMI) is associated not only with a higher incidence of breast cancers but also with poorer prognosis. It is speculated that both enhanced production of estrogens and other factors associated with obesity are involved in these associations, but the biological characteristics associated with high BMI have yet to be thoroughly identified.

Methods

We studied 525 breast cancers, focusing on biological differences between tumors associated with high and low BMI and by immunohistochemically defined intrinsic subtype. Ki67 expression levels were used to differentiate luminal A from luminal B estrogen receptor (ER)+/human epidermal growth factor receptor 2 (HER2)-breast cancers.

Results

Premenopausal patients with high BMI showed a significantly higher frequency of lymph node metastasis (46.4 % vs. 22.9 %, P = 0.005) and tended to have a larger tumor size (P = 0.05) and higher nuclear grade (P = 0.07) than those with low BMI. These differences were not observed among postmenopausal patients. BMI was not associated with distribution of breast cancer subtypes, and ER, progesterone receptor (PR), and Ki67 expression levels of each subtype showed no differences between high and low BMI among premenopausal patients.

Conclusion

Higher BMI might influence aggressive tumor characteristics among premenopausal patients, but its influence on ER, PR, and Ki67 expression levels seems to be limited.
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Metadata
Title
Influence of body mass index on clinicopathological factors including estrogen receptor, progesterone receptor, and Ki67 expression levels in breast cancers
Authors
Ayako Yanai
Yoshimasa Miyagawa
Keiko Murase
Michiko Imamura
Tomoko Yagi
Shigetoshi Ichii
Yuichi Takatsuka
Takashi Ito
Seiichi Hirota
Mitsunori Sasa
Toyomasa Katagiri
Yasuo Miyoshi
Publication date
01-06-2014
Publisher
Springer Japan
Published in
International Journal of Clinical Oncology / Issue 3/2014
Print ISSN: 1341-9625
Electronic ISSN: 1437-7772
DOI
https://doi.org/10.1007/s10147-013-0585-y

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