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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Published in | Journal of Korean medical science Vol. 22; no. 2; pp. 318 - 325 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Korea (South)
The Korean Academy of Medical Sciences
01.04.2007
대한의학회 |
Subjects | |
Online Access | Get full text |
ISSN | 1011-8934 1598-6357 |
DOI | 10.3346/jkms.2007.22.2.318 |
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Abstract | 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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AbstractList | 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. 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.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. 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. KCI Citation Count: 28 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. |
Author | Shim, Byoung Yong Cho, Kyu Do Jung, Ji Han Yoo, Jinyoung Ahn, Myeong Im Kim, Hoon Kyo Kim, Sung Hwan Kim, Chi Hong Cho, Deog Gon Kang, Seok Jin Lee, Myung A Seo, Kyung Jin |
AuthorAffiliation | Department of Internal Medicine, St. Vincent's Hospital, The Catholic University of Korea, Suwon, Korea Department of Thoracic Surgery, St. Vincent's Hospital, The Catholic University of Korea, Suwon, Korea Department of Pathology, St. Vincent's Hospital, The Catholic University of Korea, Suwon, Korea Department of Radiation Oncology, St. Vincent's Hospital, The Catholic University of Korea, Suwon, Korea Department of Diagnostic Radiology, St. Vincent's Hospital, The Catholic University of Korea, Suwon, Korea |
AuthorAffiliation_xml | – name: Department of Internal Medicine, St. Vincent's Hospital, The Catholic University of Korea, Suwon, Korea – name: Department of Pathology, St. Vincent's Hospital, The Catholic University of Korea, Suwon, Korea – name: Department of Diagnostic Radiology, St. Vincent's Hospital, The Catholic University of Korea, Suwon, Korea – name: Department of Radiation Oncology, St. Vincent's Hospital, The Catholic University of Korea, Suwon, Korea – name: Department of Thoracic Surgery, St. Vincent's Hospital, The Catholic University of Korea, Suwon, Korea |
Author_xml | – sequence: 1 givenname: Jinyoung surname: Yoo fullname: Yoo, Jinyoung organization: Department of Pathology, St. Vincent's Hospital, The Catholic University of Korea, Suwon, Korea – sequence: 2 givenname: Ji Han surname: Jung fullname: Jung, Ji Han organization: Department of Pathology, St. Vincent's Hospital, The Catholic University of Korea, Suwon, Korea – sequence: 3 givenname: Myung A surname: Lee fullname: Lee, Myung A organization: Department of Internal Medicine, St. Vincent's Hospital, The Catholic University of Korea, Suwon, Korea – sequence: 4 givenname: Kyung Jin surname: Seo fullname: Seo, Kyung Jin organization: Department of Pathology, St. Vincent's Hospital, The Catholic University of Korea, Suwon, Korea – sequence: 5 givenname: Byoung Yong surname: Shim fullname: Shim, Byoung Yong organization: Department of Internal Medicine, St. Vincent's Hospital, The Catholic University of Korea, Suwon, Korea – sequence: 6 givenname: Sung Hwan surname: Kim fullname: Kim, Sung Hwan organization: Department of Radiation Oncology, St. Vincent's Hospital, The Catholic University of Korea, Suwon, Korea – sequence: 7 givenname: Deog Gon surname: Cho fullname: Cho, Deog Gon organization: Department of Thoracic Surgery, St. Vincent's Hospital, The Catholic University of Korea, Suwon, Korea – sequence: 8 givenname: Myeong Im surname: Ahn fullname: Ahn, Myeong Im organization: Department of Diagnostic Radiology, St. Vincent's Hospital, The Catholic University of Korea, Suwon, Korea – sequence: 9 givenname: Chi Hong surname: Kim fullname: Kim, Chi Hong organization: Department of Internal Medicine, St. Vincent's Hospital, The Catholic University of Korea, Suwon, Korea – sequence: 10 givenname: Kyu Do surname: Cho fullname: Cho, Kyu Do organization: Department of Thoracic Surgery, St. Vincent's Hospital, The Catholic University of Korea, Suwon, Korea – sequence: 11 givenname: Seok Jin surname: Kang fullname: Kang, Seok Jin organization: Department of Pathology, St. Vincent's Hospital, The Catholic University of Korea, Suwon, Korea – sequence: 12 givenname: Hoon Kyo surname: Kim fullname: Kim, Hoon Kyo organization: Department of Internal Medicine, St. Vincent's Hospital, The Catholic University of Korea, Suwon, Korea |
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CitedBy_id | crossref_primary_10_1039_C4AN01978D crossref_primary_10_1097_JTO_0b013e3181e77efc crossref_primary_10_1016_j_lungcan_2012_10_008 crossref_primary_10_1016_S1578_200X_09_70011_7 crossref_primary_10_1002_cncr_25935 crossref_primary_10_1007_s10354_007_0483_x crossref_primary_10_3892_etm_2019_7392 crossref_primary_10_1016_j_arbr_2011_04_005 crossref_primary_10_3892_br_2014_319 crossref_primary_10_1007_s12253_010_9259_5 crossref_primary_10_1186_s12885_015_1524_2 crossref_primary_10_1038_labinvest_2015_1 crossref_primary_10_1016_S0212_6982_09_70209_5 crossref_primary_10_1016_j_lungcan_2011_04_019 crossref_primary_10_1186_s12931_018_0843_7 crossref_primary_10_1590_0001_3765201320120026 crossref_primary_10_2353_ajpath_2010_090500 crossref_primary_10_1016_j_humpath_2017_05_022 crossref_primary_10_1097_MD_0000000000023172 crossref_primary_10_1016_j_cca_2011_08_018 crossref_primary_10_1097_JTO_0b013e3181a97e31 crossref_primary_10_3390_cancers13164098 crossref_primary_10_1007_s11033_012_2132_8 crossref_primary_10_7314_APJCP_2014_15_20_8861 crossref_primary_10_7314_APJCP_2015_16_5_1881 crossref_primary_10_1038_labinvest_2012_101 crossref_primary_10_1097_JTO_0000000000000243 crossref_primary_10_1186_s12885_016_2304_3 crossref_primary_10_4143_crt_2012_44_1_57 crossref_primary_10_1177_1066896908323506 crossref_primary_10_1016_j_cca_2011_12_020 crossref_primary_10_5858_2008_132_384_AOITTD crossref_primary_10_1016_j_lungcan_2008_09_004 crossref_primary_10_1016_j_arbres_2011_04_010 crossref_primary_10_1007_s12105_008_0089_7 crossref_primary_10_1016_j_lungcan_2007_11_011 crossref_primary_10_1371_journal_pone_0034100 |
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Snippet | Non-small cell lung cancers (NSCLC) vary in their biologic behavior. Recurrence and tumor-related mortality may be attributable to molecular abnormalities in... |
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SubjectTerms | Aged Biomarkers, Tumor - analysis Carcinoma, Non-Small-Cell Lung - diagnosis Carcinoma, Non-Small-Cell Lung - metabolism Carcinoma, Non-Small-Cell Lung - mortality Female Humans Korea - epidemiology Lung Neoplasms - diagnosis Lung Neoplasms - metabolism Lung Neoplasms - mortality Male Neoplasm Proteins - analysis Original Outcome Assessment (Health Care) - methods Prognosis Reproducibility of Results Sensitivity and Specificity Statistics as Topic Survival Analysis Survival Rate 의학일반 |
Title | Immunohistochemical Analysis of Non-Small Cell Lung Cancer: Correlation with Clinical Parameters and Prognosis |
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