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Immunohistochemical Analysis of Non-Small Cell Lung Cancer: Correlation with Clinical Parameters and Prognosis

Non-small cell lung cancers (NSCLC) vary in their biologic behavior. Recurrence and tumor-related mortality may be attributable to molecular abnormalities in primary tumors. This study evaluated such immunophenotypes with regard to cell cycle regulation and proliferation, apoptosis, and angiogenesis...

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Autores principales: Yoo, Jinyoung, Jung, Ji Han, Lee, Myung A, Seo, Kyung Jin, Shim, Byoung Yong, Kim, Sung Hwan, Cho, Deog Gon, Ahn, Myeong Im, Kim, Chi Hong, Cho, Kyu Do, Kang, Seok Jin, Kim, Hoon Kyo
Formato: Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2693601/
https://www.ncbi.nlm.nih.gov/pubmed/17449943
http://dx.doi.org/10.3346/jkms.2007.22.2.318
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author Yoo, Jinyoung
Jung, Ji Han
Lee, Myung A
Seo, Kyung Jin
Shim, Byoung Yong
Kim, Sung Hwan
Cho, Deog Gon
Ahn, Myeong Im
Kim, Chi Hong
Cho, Kyu Do
Kang, Seok Jin
Kim, Hoon Kyo
author_facet Yoo, Jinyoung
Jung, Ji Han
Lee, Myung A
Seo, Kyung Jin
Shim, Byoung Yong
Kim, Sung Hwan
Cho, Deog Gon
Ahn, Myeong Im
Kim, Chi Hong
Cho, Kyu Do
Kang, Seok Jin
Kim, Hoon Kyo
author_sort Yoo, Jinyoung
collection PubMed
description Non-small cell lung cancers (NSCLC) vary in their biologic behavior. Recurrence and tumor-related mortality may be attributable to molecular abnormalities in primary tumors. This study evaluated such immunophenotypes with regard to cell cycle regulation and proliferation, apoptosis, and angiogenesis, to determine their significance for patient outcome. Core biopsies from 219 patients with NSCLC were assembled on tissue microarrays, and the expressions of p16, p21, p27, cyclin B1, cyclin E, Ki-67, caspase-3, survivin, bcl-2, VEGF, and endostatin were evaluated by immunohistochemistry. Despite previously described prognostic relevance of some of the investigated molecules, many of those markers were not directly associated with recurrence or survival. However, there was a trend for p16 immunoreactivity to be associated with a good prognosis (57% vs. 42% in 5-yr survival) (p=0.071). bcl-2 expression was strongly correlated with a better outcome (65% vs. 45% in 5-yr survival) (p=0.029), and the hazard of death for bcl-2 positive patients was 0.42 times of that for bcl-2 negative patients (p=0.047). A multivariate analysis with Cox proportional hazards model confirmed that the lymph node status (p=0.043) and stage (p=0.003) were other independent prognostic factors. Our results suggest that p16 and bcl-2 provide prognostic information independent of the TNM stage in NSCLC.
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spelling pubmed-26936012009-06-11 Immunohistochemical Analysis of Non-Small Cell Lung Cancer: Correlation with Clinical Parameters and Prognosis Yoo, Jinyoung Jung, Ji Han Lee, Myung A Seo, Kyung Jin Shim, Byoung Yong Kim, Sung Hwan Cho, Deog Gon Ahn, Myeong Im Kim, Chi Hong Cho, Kyu Do Kang, Seok Jin Kim, Hoon Kyo J Korean Med Sci Original Article Non-small cell lung cancers (NSCLC) vary in their biologic behavior. Recurrence and tumor-related mortality may be attributable to molecular abnormalities in primary tumors. This study evaluated such immunophenotypes with regard to cell cycle regulation and proliferation, apoptosis, and angiogenesis, to determine their significance for patient outcome. Core biopsies from 219 patients with NSCLC were assembled on tissue microarrays, and the expressions of p16, p21, p27, cyclin B1, cyclin E, Ki-67, caspase-3, survivin, bcl-2, VEGF, and endostatin were evaluated by immunohistochemistry. Despite previously described prognostic relevance of some of the investigated molecules, many of those markers were not directly associated with recurrence or survival. However, there was a trend for p16 immunoreactivity to be associated with a good prognosis (57% vs. 42% in 5-yr survival) (p=0.071). bcl-2 expression was strongly correlated with a better outcome (65% vs. 45% in 5-yr survival) (p=0.029), and the hazard of death for bcl-2 positive patients was 0.42 times of that for bcl-2 negative patients (p=0.047). A multivariate analysis with Cox proportional hazards model confirmed that the lymph node status (p=0.043) and stage (p=0.003) were other independent prognostic factors. Our results suggest that p16 and bcl-2 provide prognostic information independent of the TNM stage in NSCLC. The Korean Academy of Medical Sciences 2007-04 2007-04-30 /pmc/articles/PMC2693601/ /pubmed/17449943 http://dx.doi.org/10.3346/jkms.2007.22.2.318 Text en Copyright © 2007 The Korean Academy of Medical Sciences http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Yoo, Jinyoung
Jung, Ji Han
Lee, Myung A
Seo, Kyung Jin
Shim, Byoung Yong
Kim, Sung Hwan
Cho, Deog Gon
Ahn, Myeong Im
Kim, Chi Hong
Cho, Kyu Do
Kang, Seok Jin
Kim, Hoon Kyo
Immunohistochemical Analysis of Non-Small Cell Lung Cancer: Correlation with Clinical Parameters and Prognosis
title Immunohistochemical Analysis of Non-Small Cell Lung Cancer: Correlation with Clinical Parameters and Prognosis
title_full Immunohistochemical Analysis of Non-Small Cell Lung Cancer: Correlation with Clinical Parameters and Prognosis
title_fullStr Immunohistochemical Analysis of Non-Small Cell Lung Cancer: Correlation with Clinical Parameters and Prognosis
title_full_unstemmed Immunohistochemical Analysis of Non-Small Cell Lung Cancer: Correlation with Clinical Parameters and Prognosis
title_short Immunohistochemical Analysis of Non-Small Cell Lung Cancer: Correlation with Clinical Parameters and Prognosis
title_sort immunohistochemical analysis of non-small cell lung cancer: correlation with clinical parameters and prognosis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2693601/
https://www.ncbi.nlm.nih.gov/pubmed/17449943
http://dx.doi.org/10.3346/jkms.2007.22.2.318
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