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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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. |
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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><identifier>ISSN: 0014-4827</identifier><identifier>EISSN: 1090-2422</identifier><identifier>DOI: 10.1016/0014-4827(88)90376-X</identifier><identifier>PMID: 2457505</identifier><identifier>CODEN: ECREAL</identifier><language>eng</language><publisher>Orlando, FL: Elsevier Inc</publisher><subject>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</subject><ispartof>Experimental cell research, 1988-09, Vol.178 (1), p.41-50</ispartof><rights>1988</rights><rights>1989 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0014-4827(88)90376-X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7134377$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2457505$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/5451140$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Steigerwald, Sabine D.</creatorcontrib><creatorcontrib>Pfeifer, Gerd P.</creatorcontrib><title>Variable DNA methylation changes during differentiation of human melanoma cells</title><title>Experimental cell research</title><addtitle>Exp Cell Res</addtitle><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.</description><subject>550300 - Cytology</subject><subject>AMIDES</subject><subject>ANIMAL CELLS</subject><subject>ANIMALS</subject><subject>Aphidicolin</subject><subject>Azacitidine - analogs & 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 & 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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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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