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Increased NAD(P)H : (quinone-acceptor)oxidoreductase activity is associated with density-dependent growth inhibition of normal but not transformed cells
The activity of DT-diaphorase [NAD(P)H:(quinone-acceptor)oxidoreductase] is increased 7-fold in wild-type BALB/c 3T3T cells as they reach confluence and become density growth arrested. Harvesting and replating the cells at low density resulted in a loss of DT-diaphorase with a half time of 7 h, and...
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Published in: | Cancer research (Chicago, Ill.) Ill.), 1993-03, Vol.53 (6), p.1338-1342 |
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description | The activity of DT-diaphorase [NAD(P)H:(quinone-acceptor)oxidoreductase] is increased 7-fold in wild-type BALB/c 3T3T cells as they reach confluence and become density growth arrested. Harvesting and replating the cells at low density resulted in a loss of DT-diaphorase with a half time of 7 h, and removal of serum from high-density growth-arrested cells resulted in a decrease in DT-diaphorase with a half time of 3 days. Platelet-derived growth factor and insulin together, but not singly, maintain elevated DT-diaphorase levels in high-density growth-arrested BALB/c 3T3T cells. The increase in DT-diaphorase at high density diminished proportionately to the extent of transformation in four cell lines, 4NQO-3T3T, UV-3T3T, EJras-3T3T. and CSV3-1-3T3T. The most transformed cell line, CSV3-1-3T3T, showed no increase in DT-diaphorase at high density. Since there was no increase in DT-diaphorase mRNA in high-density growth-arrested wild-type BALB/c 3T3T cells compared to rapidly growing cells, the increase in DT-diaphorase activity at high density is most likely due to posttranslational events. High-density growth-arrested wild-type BALB/c 3T3 cells exhibited a greater sensitivity to growth inhibition by the antitumor quinone diaziquone [1,4-cyclohexadiene-1,4- dicarbamic acid, 2,5-bis(1-aziridinyl)-3,6-dioxo-, diethyl ether], which is metabolically activated by DT-diaphorase, than do low-cell-density, growth-arrested cells. The significance of the increase in DT-diaphorase at high cell density in normal cells and its loss in transformed cells may be related to the phenomenon of density-dependent growth inhibition in nontransformed but not in transformed cells. |
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J ; HOERL, B. J ; RIEBOW, J ; SCOTT, D. P ; GASDASKA, P ; SCOTT, R. E ; POWIS, G</creator><creatorcontrib>SCHLAGER, J. J ; HOERL, B. J ; RIEBOW, J ; SCOTT, D. P ; GASDASKA, P ; SCOTT, R. E ; POWIS, G</creatorcontrib><description>The activity of DT-diaphorase [NAD(P)H:(quinone-acceptor)oxidoreductase] is increased 7-fold in wild-type BALB/c 3T3T cells as they reach confluence and become density growth arrested. Harvesting and replating the cells at low density resulted in a loss of DT-diaphorase with a half time of 7 h, and removal of serum from high-density growth-arrested cells resulted in a decrease in DT-diaphorase with a half time of 3 days. Platelet-derived growth factor and insulin together, but not singly, maintain elevated DT-diaphorase levels in high-density growth-arrested BALB/c 3T3T cells. The increase in DT-diaphorase at high density diminished proportionately to the extent of transformation in four cell lines, 4NQO-3T3T, UV-3T3T, EJras-3T3T. and CSV3-1-3T3T. The most transformed cell line, CSV3-1-3T3T, showed no increase in DT-diaphorase at high density. Since there was no increase in DT-diaphorase mRNA in high-density growth-arrested wild-type BALB/c 3T3T cells compared to rapidly growing cells, the increase in DT-diaphorase activity at high density is most likely due to posttranslational events. High-density growth-arrested wild-type BALB/c 3T3 cells exhibited a greater sensitivity to growth inhibition by the antitumor quinone diaziquone [1,4-cyclohexadiene-1,4- dicarbamic acid, 2,5-bis(1-aziridinyl)-3,6-dioxo-, diethyl ether], which is metabolically activated by DT-diaphorase, than do low-cell-density, growth-arrested cells. The significance of the increase in DT-diaphorase at high cell density in normal cells and its loss in transformed cells may be related to the phenomenon of density-dependent growth inhibition in nontransformed but not in transformed cells.</description><identifier>ISSN: 0008-5472</identifier><identifier>EISSN: 1538-7445</identifier><identifier>PMID: 8443814</identifier><identifier>CODEN: CNREA8</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject>3T3 Cells - drug effects ; Animals ; Aziridines - pharmacology ; Benzoquinones - pharmacology ; Biological and medical sciences ; Blood Physiological Phenomena ; Cell Count ; Cell Division ; Cell Line, Transformed ; Cell physiology ; Cell transformation and carcinogenesis. Action of oncogenes and antioncogenes ; Cell Transformation, Neoplastic ; Fundamental and applied biological sciences. Psychology ; Growth Substances - pharmacology ; Mice ; Molecular and cellular biology ; NAD(P)H Dehydrogenase (Quinone) - genetics ; NAD(P)H Dehydrogenase (Quinone) - metabolism ; RNA, Messenger - analysis</subject><ispartof>Cancer research (Chicago, Ill.), 1993-03, Vol.53 (6), p.1338-1342</ispartof><rights>1993 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4678166$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8443814$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SCHLAGER, J. J</creatorcontrib><creatorcontrib>HOERL, B. J</creatorcontrib><creatorcontrib>RIEBOW, J</creatorcontrib><creatorcontrib>SCOTT, D. P</creatorcontrib><creatorcontrib>GASDASKA, P</creatorcontrib><creatorcontrib>SCOTT, R. E</creatorcontrib><creatorcontrib>POWIS, G</creatorcontrib><title>Increased NAD(P)H : (quinone-acceptor)oxidoreductase activity is associated with density-dependent growth inhibition of normal but not transformed cells</title><title>Cancer research (Chicago, Ill.)</title><addtitle>Cancer Res</addtitle><description>The activity of DT-diaphorase [NAD(P)H:(quinone-acceptor)oxidoreductase] is increased 7-fold in wild-type BALB/c 3T3T cells as they reach confluence and become density growth arrested. Harvesting and replating the cells at low density resulted in a loss of DT-diaphorase with a half time of 7 h, and removal of serum from high-density growth-arrested cells resulted in a decrease in DT-diaphorase with a half time of 3 days. Platelet-derived growth factor and insulin together, but not singly, maintain elevated DT-diaphorase levels in high-density growth-arrested BALB/c 3T3T cells. The increase in DT-diaphorase at high density diminished proportionately to the extent of transformation in four cell lines, 4NQO-3T3T, UV-3T3T, EJras-3T3T. and CSV3-1-3T3T. The most transformed cell line, CSV3-1-3T3T, showed no increase in DT-diaphorase at high density. Since there was no increase in DT-diaphorase mRNA in high-density growth-arrested wild-type BALB/c 3T3T cells compared to rapidly growing cells, the increase in DT-diaphorase activity at high density is most likely due to posttranslational events. High-density growth-arrested wild-type BALB/c 3T3 cells exhibited a greater sensitivity to growth inhibition by the antitumor quinone diaziquone [1,4-cyclohexadiene-1,4- dicarbamic acid, 2,5-bis(1-aziridinyl)-3,6-dioxo-, diethyl ether], which is metabolically activated by DT-diaphorase, than do low-cell-density, growth-arrested cells. The significance of the increase in DT-diaphorase at high cell density in normal cells and its loss in transformed cells may be related to the phenomenon of density-dependent growth inhibition in nontransformed but not in transformed cells.</description><subject>3T3 Cells - drug effects</subject><subject>Animals</subject><subject>Aziridines - pharmacology</subject><subject>Benzoquinones - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Blood Physiological Phenomena</subject><subject>Cell Count</subject><subject>Cell Division</subject><subject>Cell Line, Transformed</subject><subject>Cell physiology</subject><subject>Cell transformation and carcinogenesis. Action of oncogenes and antioncogenes</subject><subject>Cell Transformation, Neoplastic</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Growth Substances - pharmacology</subject><subject>Mice</subject><subject>Molecular and cellular biology</subject><subject>NAD(P)H Dehydrogenase (Quinone) - genetics</subject><subject>NAD(P)H Dehydrogenase (Quinone) - metabolism</subject><subject>RNA, Messenger - analysis</subject><issn>0008-5472</issn><issn>1538-7445</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><recordid>eNo9UE1LAzEQXUTRWv0JQg4i9rCQ3c0X3opfLYh60HOZTWZtZJu0SdbqP_HnGrE4l5k37_F4M3vFqOKNKiVjfL8YUUpVyZmsj4rjGN8z5BXlh8WhYqxRFRsV33OnA0JEQx6nN5fPkxm5IpebwTrvsAStcZ18mPhPa3xAM-iUtQR0sh82fREbCcTotYWUHbY2LYlBFzNVGlyjyyCRt-C3mbBuaVubrHfEd8T5sIKetEPKYyIpgItd3mUbjX0fT4qDDvqIp7s-Ll7vbl-uZ-XD0_38evpQLmuhUillVQtsqOlEp4F1miouaoMSa2RCGQ2dbLGuFIJiKA3DWgPmAk418rYZFxd_vuvgNwPGtFjZ-JsAHPohLiQXlNaCZuHZTji0OeViHewKwtdi98rMn-94iBr6Lh-kbfyXMSFVJUTzA-xRgio</recordid><startdate>19930315</startdate><enddate>19930315</enddate><creator>SCHLAGER, J. 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Psychology</topic><topic>Growth Substances - pharmacology</topic><topic>Mice</topic><topic>Molecular and cellular biology</topic><topic>NAD(P)H Dehydrogenase (Quinone) - genetics</topic><topic>NAD(P)H Dehydrogenase (Quinone) - metabolism</topic><topic>RNA, Messenger - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SCHLAGER, J. J</creatorcontrib><creatorcontrib>HOERL, B. J</creatorcontrib><creatorcontrib>RIEBOW, J</creatorcontrib><creatorcontrib>SCOTT, D. P</creatorcontrib><creatorcontrib>GASDASKA, P</creatorcontrib><creatorcontrib>SCOTT, R. E</creatorcontrib><creatorcontrib>POWIS, G</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>MEDLINE - Academic</collection><jtitle>Cancer research (Chicago, Ill.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SCHLAGER, J. J</au><au>HOERL, B. J</au><au>RIEBOW, J</au><au>SCOTT, D. P</au><au>GASDASKA, P</au><au>SCOTT, R. E</au><au>POWIS, G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Increased NAD(P)H : (quinone-acceptor)oxidoreductase activity is associated with density-dependent growth inhibition of normal but not transformed cells</atitle><jtitle>Cancer research (Chicago, Ill.)</jtitle><addtitle>Cancer Res</addtitle><date>1993-03-15</date><risdate>1993</risdate><volume>53</volume><issue>6</issue><spage>1338</spage><epage>1342</epage><pages>1338-1342</pages><issn>0008-5472</issn><eissn>1538-7445</eissn><coden>CNREA8</coden><abstract>The activity of DT-diaphorase [NAD(P)H:(quinone-acceptor)oxidoreductase] is increased 7-fold in wild-type BALB/c 3T3T cells as they reach confluence and become density growth arrested. Harvesting and replating the cells at low density resulted in a loss of DT-diaphorase with a half time of 7 h, and removal of serum from high-density growth-arrested cells resulted in a decrease in DT-diaphorase with a half time of 3 days. Platelet-derived growth factor and insulin together, but not singly, maintain elevated DT-diaphorase levels in high-density growth-arrested BALB/c 3T3T cells. The increase in DT-diaphorase at high density diminished proportionately to the extent of transformation in four cell lines, 4NQO-3T3T, UV-3T3T, EJras-3T3T. and CSV3-1-3T3T. The most transformed cell line, CSV3-1-3T3T, showed no increase in DT-diaphorase at high density. Since there was no increase in DT-diaphorase mRNA in high-density growth-arrested wild-type BALB/c 3T3T cells compared to rapidly growing cells, the increase in DT-diaphorase activity at high density is most likely due to posttranslational events. High-density growth-arrested wild-type BALB/c 3T3 cells exhibited a greater sensitivity to growth inhibition by the antitumor quinone diaziquone [1,4-cyclohexadiene-1,4- dicarbamic acid, 2,5-bis(1-aziridinyl)-3,6-dioxo-, diethyl ether], which is metabolically activated by DT-diaphorase, than do low-cell-density, growth-arrested cells. The significance of the increase in DT-diaphorase at high cell density in normal cells and its loss in transformed cells may be related to the phenomenon of density-dependent growth inhibition in nontransformed but not in transformed cells.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>8443814</pmid><tpages>5</tpages></addata></record> |
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subjects | 3T3 Cells - drug effects Animals Aziridines - pharmacology Benzoquinones - pharmacology Biological and medical sciences Blood Physiological Phenomena Cell Count Cell Division Cell Line, Transformed Cell physiology Cell transformation and carcinogenesis. Action of oncogenes and antioncogenes Cell Transformation, Neoplastic Fundamental and applied biological sciences. Psychology Growth Substances - pharmacology Mice Molecular and cellular biology NAD(P)H Dehydrogenase (Quinone) - genetics NAD(P)H Dehydrogenase (Quinone) - metabolism RNA, Messenger - analysis |
title | Increased NAD(P)H : (quinone-acceptor)oxidoreductase activity is associated with density-dependent growth inhibition of normal but not transformed cells |
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