Expression of Bim, Noxa, and Puma in non-small cell lung cancer

<p>Abstract</p> <p>Background</p> <p>The BH3-only members of the Bcl-2 protein family have been proposed to play a key role in the control of apoptosis and in the initiation of the apoptotic pathways. In this study, we evaluated the expression of Bim, Noxa, and Puma in...

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Main Authors: Sakakibara-Konishi Jun, Oizumi Satoshi, Kikuchi Junko, Kikuchi Eiki, Mizugaki Hidenori, Kinoshita Ichiro, Dosaka-Akita Hirotoshi, Nishimura Masaharu
Format: Article
Language:English
Published: BMC 2012-07-01
Series:BMC Cancer
Online Access:http://www.biomedcentral.com/1471-2407/12/286
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spelling doaj-8c75197be101446bb2ac2dee4823e2e42020-11-24T22:16:25ZengBMCBMC Cancer1471-24072012-07-0112128610.1186/1471-2407-12-286Expression of Bim, Noxa, and Puma in non-small cell lung cancerSakakibara-Konishi JunOizumi SatoshiKikuchi JunkoKikuchi EikiMizugaki HidenoriKinoshita IchiroDosaka-Akita HirotoshiNishimura Masaharu<p>Abstract</p> <p>Background</p> <p>The BH3-only members of the Bcl-2 protein family have been proposed to play a key role in the control of apoptosis and in the initiation of the apoptotic pathways. In this study, we evaluated the expression of Bim, Noxa, and Puma in non-small cell lung cancer (NSCLC).</p> <p>Methods</p> <p>A total of 135 surgically resected NSCLCs were immunohistochemically assessed for Bim, Noxa, and Puma expression. The immunoscores were determined, and then its correlation with either the clinicopathological variables or the survival outcomes were analyzed.</p> <p>Results</p> <p>Immunohistochemical reactivity for Bim, Noxa, and Puma was detected in the cytoplasm of the tumor cells. Bim expression was associated with several clinicopathological factors, including sex (p < 0.001), smoking habit (p = 0.03), pathological histology (p = 0.001), pathological T stage (p = 0.03), pathological disease stage (p = 0.02), and differentiation of tumor (p < 0.001). Multivariate logistic regression analysis showed a significant correlation between low Bim expression and squamous cell carcinoma (p = 0.04), in addition to a correlation between high Bim expression and well differentiated tumors (p = 0.02). Analysis of cellular biological expression demonstrated a link between low Bim expression and high Ki67. While Noxa expression was also shown to be correlated with both smoking habit (p = 0.02) and the pathological histology (p = 0.03), there was no strong association observed between the expression and the clinical features when they were examined by a multivariate logistic regression analysis. No correlations were noted between Puma expression and any of the variables. Our analyses also indicated that the expression levels of the BH3-only proteins were not pertinent to the survival outcome.</p> <p>Conclusions</p> <p>The current analyses demonstrated that Bim expression in the NSCLCs was associated with both squamous cell carcinoma histology and tumor proliferation.</p> http://www.biomedcentral.com/1471-2407/12/286
collection DOAJ
language English
format Article
sources DOAJ
author Sakakibara-Konishi Jun
Oizumi Satoshi
Kikuchi Junko
Kikuchi Eiki
Mizugaki Hidenori
Kinoshita Ichiro
Dosaka-Akita Hirotoshi
Nishimura Masaharu
spellingShingle Sakakibara-Konishi Jun
Oizumi Satoshi
Kikuchi Junko
Kikuchi Eiki
Mizugaki Hidenori
Kinoshita Ichiro
Dosaka-Akita Hirotoshi
Nishimura Masaharu
Expression of Bim, Noxa, and Puma in non-small cell lung cancer
BMC Cancer
author_facet Sakakibara-Konishi Jun
Oizumi Satoshi
Kikuchi Junko
Kikuchi Eiki
Mizugaki Hidenori
Kinoshita Ichiro
Dosaka-Akita Hirotoshi
Nishimura Masaharu
author_sort Sakakibara-Konishi Jun
title Expression of Bim, Noxa, and Puma in non-small cell lung cancer
title_short Expression of Bim, Noxa, and Puma in non-small cell lung cancer
title_full Expression of Bim, Noxa, and Puma in non-small cell lung cancer
title_fullStr Expression of Bim, Noxa, and Puma in non-small cell lung cancer
title_full_unstemmed Expression of Bim, Noxa, and Puma in non-small cell lung cancer
title_sort expression of bim, noxa, and puma in non-small cell lung cancer
publisher BMC
series BMC Cancer
issn 1471-2407
publishDate 2012-07-01
description <p>Abstract</p> <p>Background</p> <p>The BH3-only members of the Bcl-2 protein family have been proposed to play a key role in the control of apoptosis and in the initiation of the apoptotic pathways. In this study, we evaluated the expression of Bim, Noxa, and Puma in non-small cell lung cancer (NSCLC).</p> <p>Methods</p> <p>A total of 135 surgically resected NSCLCs were immunohistochemically assessed for Bim, Noxa, and Puma expression. The immunoscores were determined, and then its correlation with either the clinicopathological variables or the survival outcomes were analyzed.</p> <p>Results</p> <p>Immunohistochemical reactivity for Bim, Noxa, and Puma was detected in the cytoplasm of the tumor cells. Bim expression was associated with several clinicopathological factors, including sex (p < 0.001), smoking habit (p = 0.03), pathological histology (p = 0.001), pathological T stage (p = 0.03), pathological disease stage (p = 0.02), and differentiation of tumor (p < 0.001). Multivariate logistic regression analysis showed a significant correlation between low Bim expression and squamous cell carcinoma (p = 0.04), in addition to a correlation between high Bim expression and well differentiated tumors (p = 0.02). Analysis of cellular biological expression demonstrated a link between low Bim expression and high Ki67. While Noxa expression was also shown to be correlated with both smoking habit (p = 0.02) and the pathological histology (p = 0.03), there was no strong association observed between the expression and the clinical features when they were examined by a multivariate logistic regression analysis. No correlations were noted between Puma expression and any of the variables. Our analyses also indicated that the expression levels of the BH3-only proteins were not pertinent to the survival outcome.</p> <p>Conclusions</p> <p>The current analyses demonstrated that Bim expression in the NSCLCs was associated with both squamous cell carcinoma histology and tumor proliferation.</p>
url http://www.biomedcentral.com/1471-2407/12/286
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