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bcl-2 protein expression correlates with recurrence and survival in early stage head and neck cancer treated by radiotherapy
Inherent cellular radioresistance plays a critical role in the failure of radiation therapy (RT). The proto-oncogene bcl-2 encodes a protein that inhibits apoptosis, a common mechanism of cell death induced by several genotoxic agents, including gamma-radiation. Thus, it is likely that bcl-2 gene ex...
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Published in: | Clinical cancer research 1996-02, Vol.2 (2), p.261-267 |
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creator | Gallo, O Boddi, V Calzolari, A Simonetti, L Trovati, M Bianchi, S |
description | Inherent cellular radioresistance plays a critical role in the failure of radiation therapy (RT). The proto-oncogene bcl-2
encodes a protein that inhibits apoptosis, a common mechanism of cell death induced by several genotoxic agents, including
gamma-radiation. Thus, it is likely that bcl-2 gene expression could be involved in the complex mechanisms of radioresistance
in human tumors with some prognostic implications. In this study, we analyzed the predictive relevance of bcl-2 expression
on 5-year disease-free and overall survival in patients with early stage squamous cell carcinoma of the head and neck (SCCHN)
primary treated with RT. The expression of bcl-2 was analyzed by immunohistochemistry on paraffin-embedded sections from 71
consecutive stage I-II SCCHN patients treated with curative RT. We detected bcl-2 protein in 21% of SCCHN studied. A suggestive
association was observed between tobacco exposure and bcl-2 protein expression (P < 0.1); this association was stronger in
those patients who failed primary RT (P = 0.03). Moreover, we documented a higher rate of bcl-2 immunoreactive tumors in postirradiated
biopsies from relapsed patients than in preirradiated ones (P = 0.03). In both univariate and multivariate analyses, bcl-2
expression was the most important indicator for disease-free survival (P = 0.08 and P = 0.01, respectively) and overall survival
(P = 0.004 and P = 0.05) within 5 years of RT. The present study indicates that the proto-oncogene bcl-2 is abnormally expressed
in some SCCHN, and its expression may prove to be a useful tool in selecting patients for conventional RT with clear prognostic
implications. |
format | article |
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encodes a protein that inhibits apoptosis, a common mechanism of cell death induced by several genotoxic agents, including
gamma-radiation. Thus, it is likely that bcl-2 gene expression could be involved in the complex mechanisms of radioresistance
in human tumors with some prognostic implications. In this study, we analyzed the predictive relevance of bcl-2 expression
on 5-year disease-free and overall survival in patients with early stage squamous cell carcinoma of the head and neck (SCCHN)
primary treated with RT. The expression of bcl-2 was analyzed by immunohistochemistry on paraffin-embedded sections from 71
consecutive stage I-II SCCHN patients treated with curative RT. We detected bcl-2 protein in 21% of SCCHN studied. A suggestive
association was observed between tobacco exposure and bcl-2 protein expression (P < 0.1); this association was stronger in
those patients who failed primary RT (P = 0.03). Moreover, we documented a higher rate of bcl-2 immunoreactive tumors in postirradiated
biopsies from relapsed patients than in preirradiated ones (P = 0.03). In both univariate and multivariate analyses, bcl-2
expression was the most important indicator for disease-free survival (P = 0.08 and P = 0.01, respectively) and overall survival
(P = 0.004 and P = 0.05) within 5 years of RT. The present study indicates that the proto-oncogene bcl-2 is abnormally expressed
in some SCCHN, and its expression may prove to be a useful tool in selecting patients for conventional RT with clear prognostic
implications.</description><identifier>ISSN: 1078-0432</identifier><identifier>EISSN: 1557-3265</identifier><identifier>PMID: 9816168</identifier><language>eng</language><publisher>United States: American Association for Cancer Research</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Carcinoma, Squamous Cell - chemistry ; Carcinoma, Squamous Cell - mortality ; Carcinoma, Squamous Cell - radiotherapy ; Female ; Head and Neck Neoplasms - chemistry ; Head and Neck Neoplasms - mortality ; Head and Neck Neoplasms - radiotherapy ; Humans ; Immunohistochemistry ; Male ; Middle Aged ; Neoplasm Recurrence, Local - chemistry ; Proto-Oncogene Proteins c-bcl-2 - analysis ; Survival Rate</subject><ispartof>Clinical cancer research, 1996-02, Vol.2 (2), p.261-267</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9816168$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gallo, O</creatorcontrib><creatorcontrib>Boddi, V</creatorcontrib><creatorcontrib>Calzolari, A</creatorcontrib><creatorcontrib>Simonetti, L</creatorcontrib><creatorcontrib>Trovati, M</creatorcontrib><creatorcontrib>Bianchi, S</creatorcontrib><title>bcl-2 protein expression correlates with recurrence and survival in early stage head and neck cancer treated by radiotherapy</title><title>Clinical cancer research</title><addtitle>Clin Cancer Res</addtitle><description>Inherent cellular radioresistance plays a critical role in the failure of radiation therapy (RT). The proto-oncogene bcl-2
encodes a protein that inhibits apoptosis, a common mechanism of cell death induced by several genotoxic agents, including
gamma-radiation. Thus, it is likely that bcl-2 gene expression could be involved in the complex mechanisms of radioresistance
in human tumors with some prognostic implications. In this study, we analyzed the predictive relevance of bcl-2 expression
on 5-year disease-free and overall survival in patients with early stage squamous cell carcinoma of the head and neck (SCCHN)
primary treated with RT. The expression of bcl-2 was analyzed by immunohistochemistry on paraffin-embedded sections from 71
consecutive stage I-II SCCHN patients treated with curative RT. We detected bcl-2 protein in 21% of SCCHN studied. A suggestive
association was observed between tobacco exposure and bcl-2 protein expression (P < 0.1); this association was stronger in
those patients who failed primary RT (P = 0.03). Moreover, we documented a higher rate of bcl-2 immunoreactive tumors in postirradiated
biopsies from relapsed patients than in preirradiated ones (P = 0.03). In both univariate and multivariate analyses, bcl-2
expression was the most important indicator for disease-free survival (P = 0.08 and P = 0.01, respectively) and overall survival
(P = 0.004 and P = 0.05) within 5 years of RT. The present study indicates that the proto-oncogene bcl-2 is abnormally expressed
in some SCCHN, and its expression may prove to be a useful tool in selecting patients for conventional RT with clear prognostic
implications.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Carcinoma, Squamous Cell - chemistry</subject><subject>Carcinoma, Squamous Cell - mortality</subject><subject>Carcinoma, Squamous Cell - radiotherapy</subject><subject>Female</subject><subject>Head and Neck Neoplasms - chemistry</subject><subject>Head and Neck Neoplasms - mortality</subject><subject>Head and Neck Neoplasms - radiotherapy</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neoplasm Recurrence, Local - chemistry</subject><subject>Proto-Oncogene Proteins c-bcl-2 - analysis</subject><subject>Survival Rate</subject><issn>1078-0432</issn><issn>1557-3265</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><recordid>eNpFkM1Lw0AQxYMotVb_BGFP3gLZj2ySoxS_oOBFz2F2d7ZZTZO6m7QG_OPd2oLMYYbHbx68d5bMaZ4XKWcyP493VpRpJji7TK5C-MgyKmgmZsmsKqmkspwnP0q3KSNb3w_oOoLfW48huL4juvceWxgwkL0bGuJRj1HpNBLoDAmj37kdtOTwBb6dSBhgjaRBMH9Ah_qTaIi8J4PHaGSImogH4_qhQQ_b6Tq5sNAGvDntRfL--PC2fE5Xr08vy_tV2jBeDKkQpmLC5lLxSuRWKmOYyHglcy1ViUClNkyBljm3YCXYUmRMyMKqqrBALV8kd0ffGPNrxDDUGxc0ti102I-hLspCyozSCN6ewFFt0NRb7zbgp_pU179R49bN3nmsjwFjZ7ED3dTsMJLyXzw_d44</recordid><startdate>19960201</startdate><enddate>19960201</enddate><creator>Gallo, O</creator><creator>Boddi, V</creator><creator>Calzolari, A</creator><creator>Simonetti, L</creator><creator>Trovati, M</creator><creator>Bianchi, S</creator><general>American Association for Cancer Research</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>19960201</creationdate><title>bcl-2 protein expression correlates with recurrence and survival in early stage head and neck cancer treated by radiotherapy</title><author>Gallo, O ; Boddi, V ; Calzolari, A ; Simonetti, L ; Trovati, M ; Bianchi, S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h237t-44d924f56b3945f6bdd2403965c6b8ea16cd2bac653faf6af8402467fb97fa1f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Carcinoma, Squamous Cell - chemistry</topic><topic>Carcinoma, Squamous Cell - mortality</topic><topic>Carcinoma, Squamous Cell - radiotherapy</topic><topic>Female</topic><topic>Head and Neck Neoplasms - chemistry</topic><topic>Head and Neck Neoplasms - mortality</topic><topic>Head and Neck Neoplasms - radiotherapy</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neoplasm Recurrence, Local - chemistry</topic><topic>Proto-Oncogene Proteins c-bcl-2 - analysis</topic><topic>Survival Rate</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gallo, O</creatorcontrib><creatorcontrib>Boddi, V</creatorcontrib><creatorcontrib>Calzolari, A</creatorcontrib><creatorcontrib>Simonetti, L</creatorcontrib><creatorcontrib>Trovati, M</creatorcontrib><creatorcontrib>Bianchi, S</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical cancer research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gallo, O</au><au>Boddi, V</au><au>Calzolari, A</au><au>Simonetti, L</au><au>Trovati, M</au><au>Bianchi, S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>bcl-2 protein expression correlates with recurrence and survival in early stage head and neck cancer treated by radiotherapy</atitle><jtitle>Clinical cancer research</jtitle><addtitle>Clin Cancer Res</addtitle><date>1996-02-01</date><risdate>1996</risdate><volume>2</volume><issue>2</issue><spage>261</spage><epage>267</epage><pages>261-267</pages><issn>1078-0432</issn><eissn>1557-3265</eissn><abstract>Inherent cellular radioresistance plays a critical role in the failure of radiation therapy (RT). The proto-oncogene bcl-2
encodes a protein that inhibits apoptosis, a common mechanism of cell death induced by several genotoxic agents, including
gamma-radiation. Thus, it is likely that bcl-2 gene expression could be involved in the complex mechanisms of radioresistance
in human tumors with some prognostic implications. In this study, we analyzed the predictive relevance of bcl-2 expression
on 5-year disease-free and overall survival in patients with early stage squamous cell carcinoma of the head and neck (SCCHN)
primary treated with RT. The expression of bcl-2 was analyzed by immunohistochemistry on paraffin-embedded sections from 71
consecutive stage I-II SCCHN patients treated with curative RT. We detected bcl-2 protein in 21% of SCCHN studied. A suggestive
association was observed between tobacco exposure and bcl-2 protein expression (P < 0.1); this association was stronger in
those patients who failed primary RT (P = 0.03). Moreover, we documented a higher rate of bcl-2 immunoreactive tumors in postirradiated
biopsies from relapsed patients than in preirradiated ones (P = 0.03). In both univariate and multivariate analyses, bcl-2
expression was the most important indicator for disease-free survival (P = 0.08 and P = 0.01, respectively) and overall survival
(P = 0.004 and P = 0.05) within 5 years of RT. The present study indicates that the proto-oncogene bcl-2 is abnormally expressed
in some SCCHN, and its expression may prove to be a useful tool in selecting patients for conventional RT with clear prognostic
implications.</abstract><cop>United States</cop><pub>American Association for Cancer Research</pub><pmid>9816168</pmid><tpages>7</tpages></addata></record> |
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subjects | Adult Aged Aged, 80 and over Carcinoma, Squamous Cell - chemistry Carcinoma, Squamous Cell - mortality Carcinoma, Squamous Cell - radiotherapy Female Head and Neck Neoplasms - chemistry Head and Neck Neoplasms - mortality Head and Neck Neoplasms - radiotherapy Humans Immunohistochemistry Male Middle Aged Neoplasm Recurrence, Local - chemistry Proto-Oncogene Proteins c-bcl-2 - analysis Survival Rate |
title | bcl-2 protein expression correlates with recurrence and survival in early stage head and neck cancer treated by radiotherapy |
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