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Effect of N-acetylcysteine on the antiproliferative action of X-rays or bleomycin in cultured human lung tumor cells
N-Acetylcysteine is currently being considered as a possible selective protector against pulmonary toxicity resulting from X-rays or chemotherapeutic treatment, but its clinical application awaits evidence that it does not interfere with the efficient killing of tumor cells. The capacity of N-acetyl...
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Published in: | Journal of cancer research and clinical oncology 1989-08, Vol.115 (4), p.340-344 |
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container_end_page | 344 |
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container_title | Journal of cancer research and clinical oncology |
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creator | WANAMARTA, A. H VAN RIJN, J BLANK, L. E. C. M HAVEMAN, J VAN ZANDWIJK, N JOENJE, H |
description | N-Acetylcysteine is currently being considered as a possible selective protector against pulmonary toxicity resulting from X-rays or chemotherapeutic treatment, but its clinical application awaits evidence that it does not interfere with the efficient killing of tumor cells. The capacity of N-acetylcysteine to protect against the antitumor activity of X-rays and of bleomycin was evaluated in a clonogenic cell-survival assay using SW-1573 human squamous lung carcinoma cells as a tumor model. Using the highest non-toxic dose of N-acetylcysteine (incubation for 2 days in the continuous presence of 10 mM) no effect on clonogenic cell killing by X-rays or bleomycin treatment could be detected, even though a twofold enhancement of endogenous glutathione was effectuated. Our data thus indicate that clinically relevant concentrations of N-acetylcysteine are incapable of protecting tumor cells against clonogenic killing by X-rays and by bleomycin. |
doi_str_mv | 10.1007/bf00400960 |
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H ; VAN RIJN, J ; BLANK, L. E. C. M ; HAVEMAN, J ; VAN ZANDWIJK, N ; JOENJE, H</creator><creatorcontrib>WANAMARTA, A. H ; VAN RIJN, J ; BLANK, L. E. C. M ; HAVEMAN, J ; VAN ZANDWIJK, N ; JOENJE, H</creatorcontrib><description>N-Acetylcysteine is currently being considered as a possible selective protector against pulmonary toxicity resulting from X-rays or chemotherapeutic treatment, but its clinical application awaits evidence that it does not interfere with the efficient killing of tumor cells. The capacity of N-acetylcysteine to protect against the antitumor activity of X-rays and of bleomycin was evaluated in a clonogenic cell-survival assay using SW-1573 human squamous lung carcinoma cells as a tumor model. Using the highest non-toxic dose of N-acetylcysteine (incubation for 2 days in the continuous presence of 10 mM) no effect on clonogenic cell killing by X-rays or bleomycin treatment could be detected, even though a twofold enhancement of endogenous glutathione was effectuated. Our data thus indicate that clinically relevant concentrations of N-acetylcysteine are incapable of protecting tumor cells against clonogenic killing by X-rays and by bleomycin.</description><identifier>ISSN: 0171-5216</identifier><identifier>EISSN: 1432-1335</identifier><identifier>DOI: 10.1007/bf00400960</identifier><identifier>PMID: 2474548</identifier><identifier>CODEN: JCROD7</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Acetylcysteine - pharmacology ; Biological and medical sciences ; Bleomycin - pharmacology ; Cell Survival - drug effects ; Cell Survival - radiation effects ; Drug toxicity and drugs side effects treatment ; Glutathione - analysis ; Humans ; Lung Neoplasms - pathology ; Medical sciences ; Pharmacology. Drug treatments ; Radiation Tolerance - drug effects ; Toxicity: respiratory system, ent, stomatology ; Tumor Cells, Cultured - drug effects ; Tumor Cells, Cultured - radiation effects</subject><ispartof>Journal of cancer research and clinical oncology, 1989-08, Vol.115 (4), p.340-344</ispartof><rights>1990 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c377t-fc83fd1ed6ee3a1364346e272433eed57ba3b7bc21df7957ef74c0d2930cb6013</citedby><cites>FETCH-LOGICAL-c377t-fc83fd1ed6ee3a1364346e272433eed57ba3b7bc21df7957ef74c0d2930cb6013</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=6954687$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2474548$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>WANAMARTA, A. H</creatorcontrib><creatorcontrib>VAN RIJN, J</creatorcontrib><creatorcontrib>BLANK, L. E. C. M</creatorcontrib><creatorcontrib>HAVEMAN, J</creatorcontrib><creatorcontrib>VAN ZANDWIJK, N</creatorcontrib><creatorcontrib>JOENJE, H</creatorcontrib><title>Effect of N-acetylcysteine on the antiproliferative action of X-rays or bleomycin in cultured human lung tumor cells</title><title>Journal of cancer research and clinical oncology</title><addtitle>J Cancer Res Clin Oncol</addtitle><description>N-Acetylcysteine is currently being considered as a possible selective protector against pulmonary toxicity resulting from X-rays or chemotherapeutic treatment, but its clinical application awaits evidence that it does not interfere with the efficient killing of tumor cells. The capacity of N-acetylcysteine to protect against the antitumor activity of X-rays and of bleomycin was evaluated in a clonogenic cell-survival assay using SW-1573 human squamous lung carcinoma cells as a tumor model. Using the highest non-toxic dose of N-acetylcysteine (incubation for 2 days in the continuous presence of 10 mM) no effect on clonogenic cell killing by X-rays or bleomycin treatment could be detected, even though a twofold enhancement of endogenous glutathione was effectuated. Our data thus indicate that clinically relevant concentrations of N-acetylcysteine are incapable of protecting tumor cells against clonogenic killing by X-rays and by bleomycin.</description><subject>Acetylcysteine - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Bleomycin - pharmacology</subject><subject>Cell Survival - drug effects</subject><subject>Cell Survival - radiation effects</subject><subject>Drug toxicity and drugs side effects treatment</subject><subject>Glutathione - analysis</subject><subject>Humans</subject><subject>Lung Neoplasms - pathology</subject><subject>Medical sciences</subject><subject>Pharmacology. 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M</creator><creator>HAVEMAN, J</creator><creator>VAN ZANDWIJK, N</creator><creator>JOENJE, H</creator><general>Springer</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></search><sort><creationdate>198908</creationdate><title>Effect of N-acetylcysteine on the antiproliferative action of X-rays or bleomycin in cultured human lung tumor cells</title><author>WANAMARTA, A. H ; VAN RIJN, J ; BLANK, L. E. C. M ; HAVEMAN, J ; VAN ZANDWIJK, N ; JOENJE, H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c377t-fc83fd1ed6ee3a1364346e272433eed57ba3b7bc21df7957ef74c0d2930cb6013</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Acetylcysteine - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Bleomycin - pharmacology</topic><topic>Cell Survival - drug effects</topic><topic>Cell Survival - radiation effects</topic><topic>Drug toxicity and drugs side effects treatment</topic><topic>Glutathione - analysis</topic><topic>Humans</topic><topic>Lung Neoplasms - pathology</topic><topic>Medical sciences</topic><topic>Pharmacology. Drug treatments</topic><topic>Radiation Tolerance - drug effects</topic><topic>Toxicity: respiratory system, ent, stomatology</topic><topic>Tumor Cells, Cultured - drug effects</topic><topic>Tumor Cells, Cultured - radiation effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>WANAMARTA, A. H</creatorcontrib><creatorcontrib>VAN RIJN, J</creatorcontrib><creatorcontrib>BLANK, L. E. C. M</creatorcontrib><creatorcontrib>HAVEMAN, J</creatorcontrib><creatorcontrib>VAN ZANDWIJK, N</creatorcontrib><creatorcontrib>JOENJE, H</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><jtitle>Journal of cancer research and clinical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>WANAMARTA, A. H</au><au>VAN RIJN, J</au><au>BLANK, L. E. C. M</au><au>HAVEMAN, J</au><au>VAN ZANDWIJK, N</au><au>JOENJE, H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of N-acetylcysteine on the antiproliferative action of X-rays or bleomycin in cultured human lung tumor cells</atitle><jtitle>Journal of cancer research and clinical oncology</jtitle><addtitle>J Cancer Res Clin Oncol</addtitle><date>1989-08</date><risdate>1989</risdate><volume>115</volume><issue>4</issue><spage>340</spage><epage>344</epage><pages>340-344</pages><issn>0171-5216</issn><eissn>1432-1335</eissn><coden>JCROD7</coden><abstract>N-Acetylcysteine is currently being considered as a possible selective protector against pulmonary toxicity resulting from X-rays or chemotherapeutic treatment, but its clinical application awaits evidence that it does not interfere with the efficient killing of tumor cells. The capacity of N-acetylcysteine to protect against the antitumor activity of X-rays and of bleomycin was evaluated in a clonogenic cell-survival assay using SW-1573 human squamous lung carcinoma cells as a tumor model. Using the highest non-toxic dose of N-acetylcysteine (incubation for 2 days in the continuous presence of 10 mM) no effect on clonogenic cell killing by X-rays or bleomycin treatment could be detected, even though a twofold enhancement of endogenous glutathione was effectuated. Our data thus indicate that clinically relevant concentrations of N-acetylcysteine are incapable of protecting tumor cells against clonogenic killing by X-rays and by bleomycin.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>2474548</pmid><doi>10.1007/bf00400960</doi><tpages>5</tpages></addata></record> |
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subjects | Acetylcysteine - pharmacology Biological and medical sciences Bleomycin - pharmacology Cell Survival - drug effects Cell Survival - radiation effects Drug toxicity and drugs side effects treatment Glutathione - analysis Humans Lung Neoplasms - pathology Medical sciences Pharmacology. Drug treatments Radiation Tolerance - drug effects Toxicity: respiratory system, ent, stomatology Tumor Cells, Cultured - drug effects Tumor Cells, Cultured - radiation effects |
title | Effect of N-acetylcysteine on the antiproliferative action of X-rays or bleomycin in cultured human lung tumor cells |
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