Induction of HL-60 cell differentiation by 3-deaza-(±)-aristeromycin, an inhibitor of S-adenosylhomocysteine hydrolase

The metabolically stable inhibitor of S-adenosylhomocysteine hydrolase (AdoHcyase), 3-deaza-(+/-)-aristeromycin (dzAri) has recently been shown to induce differentiation in HL-60 cells. The present study was undertaken to characterize the cytostatic, cytotoxic, and differentiation inducing propertie...

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Veröffentlicht in:Cancer research (Chicago, Ill.) Ill.), 1986-11, Vol.46 (11), p.5469-5472
Hauptverfasser: AARBAKKE, J, MIURA, G. A, PRYTZ, P. S, BESSESEN, A, SLØRDAL, L, GORDON, R. K, CHIANG, P. K
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container_end_page 5472
container_issue 11
container_start_page 5469
container_title Cancer research (Chicago, Ill.)
container_volume 46
creator AARBAKKE, J
MIURA, G. A
PRYTZ, P. S
BESSESEN, A
SLØRDAL, L
GORDON, R. K
CHIANG, P. K
description The metabolically stable inhibitor of S-adenosylhomocysteine hydrolase (AdoHcyase), 3-deaza-(+/-)-aristeromycin (dzAri) has recently been shown to induce differentiation in HL-60 cells. The present study was undertaken to characterize the cytostatic, cytotoxic, and differentiation inducing properties of dzAri in HL-60 cells and to investigate biochemical consequences of AdoHcyase inhibition. A dye exclusion test and a clonogenic assay were used to test cytotoxic and cytostatic properties. dzAri had reversible cytostatic effects on HL-60 cells at concentrations lower than 10 microM and partially reversible cytotoxic effects above 10 microM. The induction of differentiation was dependent upon concentration and time of exposure, with maximal effect after 6 days incubation with 5-10 microM dzAri. Washout experiments demonstrated that the cells were not committed to differentiation after 48 h of incubation with dzAri. The AdoHcyase of HL-60 cells was inhibited with a Ki of 20 nM. The concentration of S-adenosylhomocysteine increased dose dependently 48 h after incubation with 0.1-100 microM dzAri. The incorporation of [3H]methyl from [methyl-3H]methionine into 5-methylcytosine of DNA was reduced by 26% at 5 microM dzAri. The findings indicate that continuous presence of dzAri is necessary to induce differentiation and inhibit proliferation in HL-60 cells. The inhibition of AdoHcyase perturbs levels of transmethylation metabolites and the incorporation of [3H]methyl into 5-methyl-cytosine of DNA.
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A ; PRYTZ, P. S ; BESSESEN, A ; SLØRDAL, L ; GORDON, R. K ; CHIANG, P. K</creator><creatorcontrib>AARBAKKE, J ; MIURA, G. A ; PRYTZ, P. S ; BESSESEN, A ; SLØRDAL, L ; GORDON, R. K ; CHIANG, P. K</creatorcontrib><description>The metabolically stable inhibitor of S-adenosylhomocysteine hydrolase (AdoHcyase), 3-deaza-(+/-)-aristeromycin (dzAri) has recently been shown to induce differentiation in HL-60 cells. The present study was undertaken to characterize the cytostatic, cytotoxic, and differentiation inducing properties of dzAri in HL-60 cells and to investigate biochemical consequences of AdoHcyase inhibition. A dye exclusion test and a clonogenic assay were used to test cytotoxic and cytostatic properties. dzAri had reversible cytostatic effects on HL-60 cells at concentrations lower than 10 microM and partially reversible cytotoxic effects above 10 microM. The induction of differentiation was dependent upon concentration and time of exposure, with maximal effect after 6 days incubation with 5-10 microM dzAri. Washout experiments demonstrated that the cells were not committed to differentiation after 48 h of incubation with dzAri. The AdoHcyase of HL-60 cells was inhibited with a Ki of 20 nM. The concentration of S-adenosylhomocysteine increased dose dependently 48 h after incubation with 0.1-100 microM dzAri. The incorporation of [3H]methyl from [methyl-3H]methionine into 5-methylcytosine of DNA was reduced by 26% at 5 microM dzAri. The findings indicate that continuous presence of dzAri is necessary to induce differentiation and inhibit proliferation in HL-60 cells. 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A dye exclusion test and a clonogenic assay were used to test cytotoxic and cytostatic properties. dzAri had reversible cytostatic effects on HL-60 cells at concentrations lower than 10 microM and partially reversible cytotoxic effects above 10 microM. The induction of differentiation was dependent upon concentration and time of exposure, with maximal effect after 6 days incubation with 5-10 microM dzAri. Washout experiments demonstrated that the cells were not committed to differentiation after 48 h of incubation with dzAri. The AdoHcyase of HL-60 cells was inhibited with a Ki of 20 nM. The concentration of S-adenosylhomocysteine increased dose dependently 48 h after incubation with 0.1-100 microM dzAri. The incorporation of [3H]methyl from [methyl-3H]methionine into 5-methylcytosine of DNA was reduced by 26% at 5 microM dzAri. The findings indicate that continuous presence of dzAri is necessary to induce differentiation and inhibit proliferation in HL-60 cells. 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S</au><au>BESSESEN, A</au><au>SLØRDAL, L</au><au>GORDON, R. K</au><au>CHIANG, P. K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Induction of HL-60 cell differentiation by 3-deaza-(±)-aristeromycin, an inhibitor of S-adenosylhomocysteine hydrolase</atitle><jtitle>Cancer research (Chicago, Ill.)</jtitle><addtitle>Cancer Res</addtitle><date>1986-11-01</date><risdate>1986</risdate><volume>46</volume><issue>11</issue><spage>5469</spage><epage>5472</epage><pages>5469-5472</pages><issn>0008-5472</issn><eissn>1538-7445</eissn><coden>CNREA8</coden><abstract>The metabolically stable inhibitor of S-adenosylhomocysteine hydrolase (AdoHcyase), 3-deaza-(+/-)-aristeromycin (dzAri) has recently been shown to induce differentiation in HL-60 cells. The present study was undertaken to characterize the cytostatic, cytotoxic, and differentiation inducing properties of dzAri in HL-60 cells and to investigate biochemical consequences of AdoHcyase inhibition. A dye exclusion test and a clonogenic assay were used to test cytotoxic and cytostatic properties. dzAri had reversible cytostatic effects on HL-60 cells at concentrations lower than 10 microM and partially reversible cytotoxic effects above 10 microM. The induction of differentiation was dependent upon concentration and time of exposure, with maximal effect after 6 days incubation with 5-10 microM dzAri. Washout experiments demonstrated that the cells were not committed to differentiation after 48 h of incubation with dzAri. The AdoHcyase of HL-60 cells was inhibited with a Ki of 20 nM. The concentration of S-adenosylhomocysteine increased dose dependently 48 h after incubation with 0.1-100 microM dzAri. The incorporation of [3H]methyl from [methyl-3H]methionine into 5-methylcytosine of DNA was reduced by 26% at 5 microM dzAri. The findings indicate that continuous presence of dzAri is necessary to induce differentiation and inhibit proliferation in HL-60 cells. The inhibition of AdoHcyase perturbs levels of transmethylation metabolites and the incorporation of [3H]methyl into 5-methyl-cytosine of DNA.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>3463413</pmid><tpages>4</tpages></addata></record>
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source MEDLINE; American Association for Cancer Research; EZB-FREE-00999 freely available EZB journals
subjects Adenosine - analogs & derivatives
Adenosine - pharmacology
Adenosylhomocysteinase
Antineoplastic agents
Biological and medical sciences
Cell Cycle - drug effects
Cell Differentiation - drug effects
Cell Line
Cell Survival - drug effects
General aspects
Humans
Hydrolases - antagonists & inhibitors
Leukemia, Myeloid, Acute
Medical sciences
Pharmacology. Drug treatments
S-Adenosylhomocysteine - metabolism
S-Adenosylmethionine - metabolism
title Induction of HL-60 cell differentiation by 3-deaza-(±)-aristeromycin, an inhibitor of S-adenosylhomocysteine hydrolase
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