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Reduced poly(ADP‐ribosyl)ation in lymphocytes of laryngeal cancer patients: Results of a case‐control study
Poly(ADP‐ribose) polymerase (PARP), a nuclear enzyme that is catalytically activated by DNA strand breaks, plays a complex role in DNA repair. Using NAD+ as a precursor, it catalyzes the formation of ADP‐ribose polymers, which are attached to various proteins. Defects in DNA repair pathways have bee...
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Published in: | International journal of cancer 2002-04, Vol.98 (5), p.780-784 |
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description | Poly(ADP‐ribose) polymerase (PARP), a nuclear enzyme that is catalytically activated by DNA strand breaks, plays a complex role in DNA repair. Using NAD+ as a precursor, it catalyzes the formation of ADP‐ribose polymers, which are attached to various proteins. Defects in DNA repair pathways have been associated with increased risks for cancer in humans. We investigated whether differences in the activity of PARP are associated with the risk for laryngeal cancer. In a case‐control study on genetic, lifestyle and occupational risk factors for laryngeal cancer, PARP activity was assessed as DNA damage–induced poly(ADP‐ribose) formation in human peripheral blood lymphocytes by quantitative immunofluorescence analysis. Polymer formation was determined as the cellular response to bleomycin, a well‐known inducer of DNA strand breaks, in lymphocytes from 69 laryngeal cancer patients and 125 healthy controls. The frequency of bleomycin‐induced polymer formation, measured as mean pixel intensity, was significantly lower in cases (74.6, SE = 3.7) than in controls (94.5, SE = 3.5) and not influenced by smoking, age or sex. There was no significant difference between cases (59.1, SE = 5.2) and controls (50.5, SE = 3.7) in basal polymer formation (in cells not treated with bleomycin). When the highest tertile of polymer formation was used as the reference, the odds ratio for the lowest tertile of bleomycin‐induced polymer formation was 3.79 (95% confidence interval 1.37–10.47, p = 0.01). Peripheral blood lymphocytes from laryngeal cancer patients thus showed significantly less bleomycin‐induced poly(ADP‐ribose) formation. Our results suggest that a reduced capacity of somatic cells to synthesize poly(ADP‐ribose) might be associated with an increased risk for laryngeal cancer. The underlying mechanism remains to be investigated. © 2002 Wiley‐Liss, Inc. |
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Using NAD+ as a precursor, it catalyzes the formation of ADP‐ribose polymers, which are attached to various proteins. Defects in DNA repair pathways have been associated with increased risks for cancer in humans. We investigated whether differences in the activity of PARP are associated with the risk for laryngeal cancer. In a case‐control study on genetic, lifestyle and occupational risk factors for laryngeal cancer, PARP activity was assessed as DNA damage–induced poly(ADP‐ribose) formation in human peripheral blood lymphocytes by quantitative immunofluorescence analysis. Polymer formation was determined as the cellular response to bleomycin, a well‐known inducer of DNA strand breaks, in lymphocytes from 69 laryngeal cancer patients and 125 healthy controls. The frequency of bleomycin‐induced polymer formation, measured as mean pixel intensity, was significantly lower in cases (74.6, SE = 3.7) than in controls (94.5, SE = 3.5) and not influenced by smoking, age or sex. There was no significant difference between cases (59.1, SE = 5.2) and controls (50.5, SE = 3.7) in basal polymer formation (in cells not treated with bleomycin). When the highest tertile of polymer formation was used as the reference, the odds ratio for the lowest tertile of bleomycin‐induced polymer formation was 3.79 (95% confidence interval 1.37–10.47, p = 0.01). Peripheral blood lymphocytes from laryngeal cancer patients thus showed significantly less bleomycin‐induced poly(ADP‐ribose) formation. Our results suggest that a reduced capacity of somatic cells to synthesize poly(ADP‐ribose) might be associated with an increased risk for laryngeal cancer. The underlying mechanism remains to be investigated. © 2002 Wiley‐Liss, Inc.</description><identifier>ISSN: 0020-7136</identifier><identifier>EISSN: 1097-0215</identifier><identifier>DOI: 10.1002/ijc.10234</identifier><identifier>PMID: 11920651</identifier><identifier>CODEN: IJCNAW</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Antibiotics, Antineoplastic - pharmacology ; Biological and medical sciences ; biomarker ; bleomycin ; Bleomycin - pharmacology ; Case-Control Studies ; DNA Damage ; DNA, Neoplasm - drug effects ; Female ; Fluorescent Antibody Technique - methods ; Humans ; Image Processing, Computer-Assisted - methods ; laryngeal cancer ; Laryngeal Neoplasms - metabolism ; Laryngeal Neoplasms - pathology ; Lymphocytes - drug effects ; Lymphocytes - metabolism ; Male ; Medical sciences ; Middle Aged ; molecular epidemiology ; Otorhinolaryngology. Stomatology ; Poly Adenosine Diphosphate Ribose - metabolism ; Poly(ADP-ribose) Polymerases - metabolism ; poly(ADP‐ribose) polymerase ; Tumors ; Upper respiratory tract, upper alimentary tract, paranasal sinuses, salivary glands: diseases, semeiology</subject><ispartof>International journal of cancer, 2002-04, Vol.98 (5), p.780-784</ispartof><rights>Copyright © 2002 Wiley‐Liss, Inc.</rights><rights>2002 INIST-CNRS</rights><rights>Copyright 2002 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3864-456f2069837cd2aa1b4d94a82d7c86fda770e366139375c72e3b424072df441a3</citedby><cites>FETCH-LOGICAL-c3864-456f2069837cd2aa1b4d94a82d7c86fda770e366139375c72e3b424072df441a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13587366$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11920651$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rajaee‐Behbahani, Nahid</creatorcontrib><creatorcontrib>Schmezer, Peter</creatorcontrib><creatorcontrib>Ramroth, Heribert</creatorcontrib><creatorcontrib>Bürkle, Alexander</creatorcontrib><creatorcontrib>Bartsch, Helmut</creatorcontrib><creatorcontrib>Dietz, Andreas</creatorcontrib><creatorcontrib>Becher, Heiko</creatorcontrib><title>Reduced poly(ADP‐ribosyl)ation in lymphocytes of laryngeal cancer patients: Results of a case‐control study</title><title>International journal of cancer</title><addtitle>Int J Cancer</addtitle><description>Poly(ADP‐ribose) polymerase (PARP), a nuclear enzyme that is catalytically activated by DNA strand breaks, plays a complex role in DNA repair. Using NAD+ as a precursor, it catalyzes the formation of ADP‐ribose polymers, which are attached to various proteins. Defects in DNA repair pathways have been associated with increased risks for cancer in humans. We investigated whether differences in the activity of PARP are associated with the risk for laryngeal cancer. In a case‐control study on genetic, lifestyle and occupational risk factors for laryngeal cancer, PARP activity was assessed as DNA damage–induced poly(ADP‐ribose) formation in human peripheral blood lymphocytes by quantitative immunofluorescence analysis. Polymer formation was determined as the cellular response to bleomycin, a well‐known inducer of DNA strand breaks, in lymphocytes from 69 laryngeal cancer patients and 125 healthy controls. The frequency of bleomycin‐induced polymer formation, measured as mean pixel intensity, was significantly lower in cases (74.6, SE = 3.7) than in controls (94.5, SE = 3.5) and not influenced by smoking, age or sex. There was no significant difference between cases (59.1, SE = 5.2) and controls (50.5, SE = 3.7) in basal polymer formation (in cells not treated with bleomycin). When the highest tertile of polymer formation was used as the reference, the odds ratio for the lowest tertile of bleomycin‐induced polymer formation was 3.79 (95% confidence interval 1.37–10.47, p = 0.01). Peripheral blood lymphocytes from laryngeal cancer patients thus showed significantly less bleomycin‐induced poly(ADP‐ribose) formation. Our results suggest that a reduced capacity of somatic cells to synthesize poly(ADP‐ribose) might be associated with an increased risk for laryngeal cancer. The underlying mechanism remains to be investigated. © 2002 Wiley‐Liss, Inc.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antibiotics, Antineoplastic - pharmacology</subject><subject>Biological and medical sciences</subject><subject>biomarker</subject><subject>bleomycin</subject><subject>Bleomycin - pharmacology</subject><subject>Case-Control Studies</subject><subject>DNA Damage</subject><subject>DNA, Neoplasm - drug effects</subject><subject>Female</subject><subject>Fluorescent Antibody Technique - methods</subject><subject>Humans</subject><subject>Image Processing, Computer-Assisted - methods</subject><subject>laryngeal cancer</subject><subject>Laryngeal Neoplasms - metabolism</subject><subject>Laryngeal Neoplasms - pathology</subject><subject>Lymphocytes - drug effects</subject><subject>Lymphocytes - metabolism</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>molecular epidemiology</subject><subject>Otorhinolaryngology. Stomatology</subject><subject>Poly Adenosine Diphosphate Ribose - metabolism</subject><subject>Poly(ADP-ribose) Polymerases - metabolism</subject><subject>poly(ADP‐ribose) polymerase</subject><subject>Tumors</subject><subject>Upper respiratory tract, upper alimentary tract, paranasal sinuses, salivary glands: diseases, semeiology</subject><issn>0020-7136</issn><issn>1097-0215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNp10MtO3DAUBmALFcFwWfAClTetmEXAx3bipDs00AJCokJlHXnsExrkiVM7UZUdj8Az8iR1Z0ZixcqWzqdz-Qk5AXYGjPHz9tmkDxdyh8yAVSpjHPJPZJZqLFMgin1yEOMzYwA5k3tkH6DirMhhRvwD2tGgpb130-nF5c-3l9fQLn2c3FwPre9o21E3rfrf3kwDRuob6nSYuifUjhrdGQy0TxK7IX6jDxhHN6yVTtWIqZ3x3RC8o3EY7XREdhvtIh5v30Py-P3q1-I6u7v_cbO4uMuMKAuZybxo0oZVKZSxXGtYSltJXXKrTFk0VivFUBQFiEqo3CiOYim5ZIrbRkrQ4pB83fTtg_8zYhzqVRsNOqc79GOsFeQyhwoSnG-gCT7GgE3dh3aVLqyB1f_TrVO69TrdZD9vm47LFdp3uY0zgS9boKPRrgkpnza-O5GXKm2d3PnG_W0dTh9PrG9uF5vR_wBPpZKG</recordid><startdate>20020410</startdate><enddate>20020410</enddate><creator>Rajaee‐Behbahani, Nahid</creator><creator>Schmezer, Peter</creator><creator>Ramroth, Heribert</creator><creator>Bürkle, Alexander</creator><creator>Bartsch, Helmut</creator><creator>Dietz, Andreas</creator><creator>Becher, Heiko</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20020410</creationdate><title>Reduced poly(ADP‐ribosyl)ation in lymphocytes of laryngeal cancer patients: Results of a case‐control study</title><author>Rajaee‐Behbahani, Nahid ; Schmezer, Peter ; Ramroth, Heribert ; Bürkle, Alexander ; Bartsch, Helmut ; Dietz, Andreas ; Becher, Heiko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3864-456f2069837cd2aa1b4d94a82d7c86fda770e366139375c72e3b424072df441a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antibiotics, Antineoplastic - pharmacology</topic><topic>Biological and medical sciences</topic><topic>biomarker</topic><topic>bleomycin</topic><topic>Bleomycin - pharmacology</topic><topic>Case-Control Studies</topic><topic>DNA Damage</topic><topic>DNA, Neoplasm - drug effects</topic><topic>Female</topic><topic>Fluorescent Antibody Technique - methods</topic><topic>Humans</topic><topic>Image Processing, Computer-Assisted - methods</topic><topic>laryngeal cancer</topic><topic>Laryngeal Neoplasms - metabolism</topic><topic>Laryngeal Neoplasms - pathology</topic><topic>Lymphocytes - drug effects</topic><topic>Lymphocytes - metabolism</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>molecular epidemiology</topic><topic>Otorhinolaryngology. Stomatology</topic><topic>Poly Adenosine Diphosphate Ribose - metabolism</topic><topic>Poly(ADP-ribose) Polymerases - metabolism</topic><topic>poly(ADP‐ribose) polymerase</topic><topic>Tumors</topic><topic>Upper respiratory tract, upper alimentary tract, paranasal sinuses, salivary glands: diseases, semeiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rajaee‐Behbahani, Nahid</creatorcontrib><creatorcontrib>Schmezer, Peter</creatorcontrib><creatorcontrib>Ramroth, Heribert</creatorcontrib><creatorcontrib>Bürkle, Alexander</creatorcontrib><creatorcontrib>Bartsch, Helmut</creatorcontrib><creatorcontrib>Dietz, Andreas</creatorcontrib><creatorcontrib>Becher, Heiko</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rajaee‐Behbahani, Nahid</au><au>Schmezer, Peter</au><au>Ramroth, Heribert</au><au>Bürkle, Alexander</au><au>Bartsch, Helmut</au><au>Dietz, Andreas</au><au>Becher, Heiko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reduced poly(ADP‐ribosyl)ation in lymphocytes of laryngeal cancer patients: Results of a case‐control study</atitle><jtitle>International journal of cancer</jtitle><addtitle>Int J Cancer</addtitle><date>2002-04-10</date><risdate>2002</risdate><volume>98</volume><issue>5</issue><spage>780</spage><epage>784</epage><pages>780-784</pages><issn>0020-7136</issn><eissn>1097-0215</eissn><coden>IJCNAW</coden><abstract>Poly(ADP‐ribose) polymerase (PARP), a nuclear enzyme that is catalytically activated by DNA strand breaks, plays a complex role in DNA repair. Using NAD+ as a precursor, it catalyzes the formation of ADP‐ribose polymers, which are attached to various proteins. Defects in DNA repair pathways have been associated with increased risks for cancer in humans. We investigated whether differences in the activity of PARP are associated with the risk for laryngeal cancer. In a case‐control study on genetic, lifestyle and occupational risk factors for laryngeal cancer, PARP activity was assessed as DNA damage–induced poly(ADP‐ribose) formation in human peripheral blood lymphocytes by quantitative immunofluorescence analysis. Polymer formation was determined as the cellular response to bleomycin, a well‐known inducer of DNA strand breaks, in lymphocytes from 69 laryngeal cancer patients and 125 healthy controls. The frequency of bleomycin‐induced polymer formation, measured as mean pixel intensity, was significantly lower in cases (74.6, SE = 3.7) than in controls (94.5, SE = 3.5) and not influenced by smoking, age or sex. There was no significant difference between cases (59.1, SE = 5.2) and controls (50.5, SE = 3.7) in basal polymer formation (in cells not treated with bleomycin). When the highest tertile of polymer formation was used as the reference, the odds ratio for the lowest tertile of bleomycin‐induced polymer formation was 3.79 (95% confidence interval 1.37–10.47, p = 0.01). Peripheral blood lymphocytes from laryngeal cancer patients thus showed significantly less bleomycin‐induced poly(ADP‐ribose) formation. Our results suggest that a reduced capacity of somatic cells to synthesize poly(ADP‐ribose) might be associated with an increased risk for laryngeal cancer. The underlying mechanism remains to be investigated. © 2002 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>11920651</pmid><doi>10.1002/ijc.10234</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Aged, 80 and over Antibiotics, Antineoplastic - pharmacology Biological and medical sciences biomarker bleomycin Bleomycin - pharmacology Case-Control Studies DNA Damage DNA, Neoplasm - drug effects Female Fluorescent Antibody Technique - methods Humans Image Processing, Computer-Assisted - methods laryngeal cancer Laryngeal Neoplasms - metabolism Laryngeal Neoplasms - pathology Lymphocytes - drug effects Lymphocytes - metabolism Male Medical sciences Middle Aged molecular epidemiology Otorhinolaryngology. Stomatology Poly Adenosine Diphosphate Ribose - metabolism Poly(ADP-ribose) Polymerases - metabolism poly(ADP‐ribose) polymerase Tumors Upper respiratory tract, upper alimentary tract, paranasal sinuses, salivary glands: diseases, semeiology |
title | Reduced poly(ADP‐ribosyl)ation in lymphocytes of laryngeal cancer patients: Results of a case‐control study |
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