Variable DNA methylation changes during differentiation of human melanoma cells

The DNA 5-methylcytosine content has been analyzed in the human melanoma cell line M21 at several time points after induction of differentiation by a variety of inducers. 5-Aza-2′-deoxycytidine reduces DNA methylation to about 50% of the control level and this demethylation occurs prior to the estab...

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Veröffentlicht in:Experimental cell research 1988-09, Vol.178 (1), p.41-50
Hauptverfasser: Steigerwald, Sabine D., Pfeifer, Gerd P.
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description The DNA 5-methylcytosine content has been analyzed in the human melanoma cell line M21 at several time points after induction of differentiation by a variety of inducers. 5-Aza-2′-deoxycytidine reduces DNA methylation to about 50% of the control level and this demethylation occurs prior to the establishment of the differentiated phenotype. The DNA synthesis inhibitors cytosine arabinoside, aphidicolin, and hydroxyurea exert different effects on DNA methylation in these cells. Cytosine arabinoside induces an early DNA hypermethylation, which is however reversible and drops to the original level after 24 h. Hydroxyurea induces DNA hypermethylation after a lag period of more than 48 h and the DNA polymerase α inhibitor aphidicolin has no effect on the DNA methylation level. Treatment of cells with phorbol 12-myristate 13-acetate, another potent inducer of melanoma cell differentiation, does not result in a change of total DNA methylation over a period of 96 h. These results indicate that differentiation of human melanoma cells can be accompanied by variable changes of the DNA methylation pattern. These changes can be neither generally related to the differentiation process itself nor related to the effects of DNA synthesis inhibition on DNA methylation, but may more likely reflect a direct or indirect particular effect of the inducer on the DNA methylation process.
doi_str_mv 10.1016/0014-4827(88)90376-X
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The DNA synthesis inhibitors cytosine arabinoside, aphidicolin, and hydroxyurea exert different effects on DNA methylation in these cells. Cytosine arabinoside induces an early DNA hypermethylation, which is however reversible and drops to the original level after 24 h. Hydroxyurea induces DNA hypermethylation after a lag period of more than 48 h and the DNA polymerase α inhibitor aphidicolin has no effect on the DNA methylation level. Treatment of cells with phorbol 12-myristate 13-acetate, another potent inducer of melanoma cell differentiation, does not result in a change of total DNA methylation over a period of 96 h. These results indicate that differentiation of human melanoma cells can be accompanied by variable changes of the DNA methylation pattern. 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The DNA synthesis inhibitors cytosine arabinoside, aphidicolin, and hydroxyurea exert different effects on DNA methylation in these cells. Cytosine arabinoside induces an early DNA hypermethylation, which is however reversible and drops to the original level after 24 h. Hydroxyurea induces DNA hypermethylation after a lag period of more than 48 h and the DNA polymerase α inhibitor aphidicolin has no effect on the DNA methylation level. Treatment of cells with phorbol 12-myristate 13-acetate, another potent inducer of melanoma cell differentiation, does not result in a change of total DNA methylation over a period of 96 h. These results indicate that differentiation of human melanoma cells can be accompanied by variable changes of the DNA methylation pattern. These changes can be neither generally related to the differentiation process itself nor related to the effects of DNA synthesis inhibition on DNA methylation, but may more likely reflect a direct or indirect particular effect of the inducer on the DNA methylation process.</description><subject>550300 - Cytology</subject><subject>AMIDES</subject><subject>ANIMAL CELLS</subject><subject>ANIMALS</subject><subject>Aphidicolin</subject><subject>Azacitidine - analogs &amp; derivatives</subject><subject>Azacitidine - pharmacology</subject><subject>BASIC BIOLOGICAL SCIENCES</subject><subject>Biological and medical sciences</subject><subject>CARCINOGENS</subject><subject>CELL DIFFERENTIATION</subject><subject>Cell Differentiation - drug effects</subject><subject>Cell differentiation, maturation, development, hematopoiesis</subject><subject>Cell Division - drug effects</subject><subject>Cell physiology</subject><subject>CHEMICAL REACTIONS</subject><subject>CHROMATOGRAPHY</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Cytarabine - pharmacology</subject><subject>Decitabine</subject><subject>DISEASES</subject><subject>Diterpenes - pharmacology</subject><subject>DNA</subject><subject>DNA - drug effects</subject><subject>DNA - metabolism</subject><subject>DNA METHYLASES</subject><subject>DNA, Neoplasm - drug effects</subject><subject>DNA, Neoplasm - metabolism</subject><subject>ENZYMES</subject><subject>ESTERS</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>HYDROXY COMPOUNDS</subject><subject>HYDROXYUREA</subject><subject>Hydroxyurea - pharmacology</subject><subject>LYASES</subject><subject>MAMMALS</subject><subject>MAN</subject><subject>MELANOMAS</subject><subject>METHYLATION</subject><subject>Molecular and cellular biology</subject><subject>Monophenol Monooxygenase - metabolism</subject><subject>NEOPLASMS</subject><subject>NUCLEIC ACIDS</subject><subject>NUCLEOPROTEINS</subject><subject>ORGANIC COMPOUNDS</subject><subject>ORGANIC NITROGEN COMPOUNDS</subject><subject>PHORBOL ESTERS</subject><subject>PRIMATES</subject><subject>PROTEINS</subject><subject>SEPARATION PROCESSES</subject><subject>Tetradecanoylphorbol Acetate - pharmacology</subject><subject>THIN-LAYER CHROMATOGRAPHY</subject><subject>TUMOR CELLS</subject><subject>Tumor Cells, Cultured</subject><subject>VERTEBRATES</subject><issn>0014-4827</issn><issn>1090-2422</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kU1v1DAQhi0EKtvCPwApQlUFh8A4tmPnglSVr0pVewHUmzVrj7tGiVPspFL_PQm76mkO72PrnXkYe8PhIwfefgLgspam0e-N-dCB0G19-4xtOHRQN7JpnrPNE_KSHZfyBwCM4e0RO2qk0grUht38xhxx21P15fq8GmjaPfY4xTFVbofpjkrl5xzTXeVjCJQpTXEfj6HazQOm5U2PaRywctT35RV7EbAv9PowT9ivb19_Xvyor26-X16cX9UkpJlqGToueIdeIgTBDcoALmyl1zpI55zXpIA6uVXO8IAahGn9QjUqeE66ESfs3f7fsUzRFhcncjs3pkRuskoqziUs0Nkeus_j35nKZIdY1pqYaJyL5QraVkm5gG8P4LwdyNv7HAfMj_ZwpiU_PeRYHPYhY3KxPGGaCym0XrDPe4yWzR8i5bUYJUc-5rWXH6PlYFd7dlVjVzXWGPvfnr0V_wALsort</recordid><startdate>19880901</startdate><enddate>19880901</enddate><creator>Steigerwald, Sabine D.</creator><creator>Pfeifer, Gerd P.</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7TM</scope><scope>OTOTI</scope></search><sort><creationdate>19880901</creationdate><title>Variable DNA methylation changes during differentiation of human melanoma cells</title><author>Steigerwald, Sabine D. ; Pfeifer, Gerd P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-e348t-4f91319ad4a0f318a4f0cfb4d77f4cccd7e50e94b5c81fa70386d8a425fd1e723</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1988</creationdate><topic>550300 - Cytology</topic><topic>AMIDES</topic><topic>ANIMAL CELLS</topic><topic>ANIMALS</topic><topic>Aphidicolin</topic><topic>Azacitidine - analogs &amp; derivatives</topic><topic>Azacitidine - pharmacology</topic><topic>BASIC BIOLOGICAL SCIENCES</topic><topic>Biological and medical sciences</topic><topic>CARCINOGENS</topic><topic>CELL DIFFERENTIATION</topic><topic>Cell Differentiation - drug effects</topic><topic>Cell differentiation, maturation, development, hematopoiesis</topic><topic>Cell Division - drug effects</topic><topic>Cell physiology</topic><topic>CHEMICAL REACTIONS</topic><topic>CHROMATOGRAPHY</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Cytarabine - pharmacology</topic><topic>Decitabine</topic><topic>DISEASES</topic><topic>Diterpenes - pharmacology</topic><topic>DNA</topic><topic>DNA - drug effects</topic><topic>DNA - metabolism</topic><topic>DNA METHYLASES</topic><topic>DNA, Neoplasm - drug effects</topic><topic>DNA, Neoplasm - metabolism</topic><topic>ENZYMES</topic><topic>ESTERS</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>HYDROXY COMPOUNDS</topic><topic>HYDROXYUREA</topic><topic>Hydroxyurea - pharmacology</topic><topic>LYASES</topic><topic>MAMMALS</topic><topic>MAN</topic><topic>MELANOMAS</topic><topic>METHYLATION</topic><topic>Molecular and cellular biology</topic><topic>Monophenol Monooxygenase - metabolism</topic><topic>NEOPLASMS</topic><topic>NUCLEIC ACIDS</topic><topic>NUCLEOPROTEINS</topic><topic>ORGANIC COMPOUNDS</topic><topic>ORGANIC NITROGEN COMPOUNDS</topic><topic>PHORBOL ESTERS</topic><topic>PRIMATES</topic><topic>PROTEINS</topic><topic>SEPARATION PROCESSES</topic><topic>Tetradecanoylphorbol Acetate - pharmacology</topic><topic>THIN-LAYER CHROMATOGRAPHY</topic><topic>TUMOR CELLS</topic><topic>Tumor Cells, Cultured</topic><topic>VERTEBRATES</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Steigerwald, Sabine D.</creatorcontrib><creatorcontrib>Pfeifer, Gerd P.</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>Nucleic Acids Abstracts</collection><collection>OSTI.GOV</collection><jtitle>Experimental cell research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Steigerwald, Sabine D.</au><au>Pfeifer, Gerd P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Variable DNA methylation changes during differentiation of human melanoma cells</atitle><jtitle>Experimental cell research</jtitle><addtitle>Exp Cell Res</addtitle><date>1988-09-01</date><risdate>1988</risdate><volume>178</volume><issue>1</issue><spage>41</spage><epage>50</epage><pages>41-50</pages><issn>0014-4827</issn><eissn>1090-2422</eissn><coden>ECREAL</coden><abstract>The DNA 5-methylcytosine content has been analyzed in the human melanoma cell line M21 at several time points after induction of differentiation by a variety of inducers. 5-Aza-2′-deoxycytidine reduces DNA methylation to about 50% of the control level and this demethylation occurs prior to the establishment of the differentiated phenotype. The DNA synthesis inhibitors cytosine arabinoside, aphidicolin, and hydroxyurea exert different effects on DNA methylation in these cells. Cytosine arabinoside induces an early DNA hypermethylation, which is however reversible and drops to the original level after 24 h. Hydroxyurea induces DNA hypermethylation after a lag period of more than 48 h and the DNA polymerase α inhibitor aphidicolin has no effect on the DNA methylation level. Treatment of cells with phorbol 12-myristate 13-acetate, another potent inducer of melanoma cell differentiation, does not result in a change of total DNA methylation over a period of 96 h. These results indicate that differentiation of human melanoma cells can be accompanied by variable changes of the DNA methylation pattern. These changes can be neither generally related to the differentiation process itself nor related to the effects of DNA synthesis inhibition on DNA methylation, but may more likely reflect a direct or indirect particular effect of the inducer on the DNA methylation process.</abstract><cop>Orlando, FL</cop><pub>Elsevier Inc</pub><pmid>2457505</pmid><doi>10.1016/0014-4827(88)90376-X</doi><tpages>10</tpages></addata></record>
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ispartof Experimental cell research, 1988-09, Vol.178 (1), p.41-50
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subjects 550300 - Cytology
AMIDES
ANIMAL CELLS
ANIMALS
Aphidicolin
Azacitidine - analogs & derivatives
Azacitidine - pharmacology
BASIC BIOLOGICAL SCIENCES
Biological and medical sciences
CARCINOGENS
CELL DIFFERENTIATION
Cell Differentiation - drug effects
Cell differentiation, maturation, development, hematopoiesis
Cell Division - drug effects
Cell physiology
CHEMICAL REACTIONS
CHROMATOGRAPHY
Chromatography, High Pressure Liquid
Cytarabine - pharmacology
Decitabine
DISEASES
Diterpenes - pharmacology
DNA
DNA - drug effects
DNA - metabolism
DNA METHYLASES
DNA, Neoplasm - drug effects
DNA, Neoplasm - metabolism
ENZYMES
ESTERS
Fundamental and applied biological sciences. Psychology
Humans
HYDROXY COMPOUNDS
HYDROXYUREA
Hydroxyurea - pharmacology
LYASES
MAMMALS
MAN
MELANOMAS
METHYLATION
Molecular and cellular biology
Monophenol Monooxygenase - metabolism
NEOPLASMS
NUCLEIC ACIDS
NUCLEOPROTEINS
ORGANIC COMPOUNDS
ORGANIC NITROGEN COMPOUNDS
PHORBOL ESTERS
PRIMATES
PROTEINS
SEPARATION PROCESSES
Tetradecanoylphorbol Acetate - pharmacology
THIN-LAYER CHROMATOGRAPHY
TUMOR CELLS
Tumor Cells, Cultured
VERTEBRATES
title Variable DNA methylation changes during differentiation of human melanoma cells
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