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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
Main Authors: SCHLAGER, J. J, HOERL, B. J, RIEBOW, J, SCOTT, D. P, GASDASKA, P, SCOTT, R. E, POWIS, G
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container_issue 6
container_start_page 1338
container_title Cancer research (Chicago, Ill.)
container_volume 53
creator SCHLAGER, J. J
HOERL, B. J
RIEBOW, J
SCOTT, D. P
GASDASKA, P
SCOTT, R. E
POWIS, G
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. 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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. 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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. 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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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source EZB-FREE-00999 freely available EZB journals
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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