Effects of 50 Hz magnetic fields on C-myc transcript levels in nonsynchronized and synchronized human cells
The effects of 50 Hz electromagnetic fields (EMFs) on the expression of the c‐myc oncogene, known to be involved in normal cell proliferation and possibly also in tumor processes, were investigated in nonsynchronized human lymphoid cells immortalized by Epstein‐Barr virus. Viral injury to such cells...
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Veröffentlicht in: | Bioelectromagnetics 1995, Vol.16 (5), p.277-283 |
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description | The effects of 50 Hz electromagnetic fields (EMFs) on the expression of the c‐myc oncogene, known to be involved in normal cell proliferation and possibly also in tumor processes, were investigated in nonsynchronized human lymphoid cells immortalized by Epstein‐Barr virus. Viral injury to such cells makes them a good model for exploring the possible cancer‐promoting effects of 50 Hz magnetic fields. Parallel experiments were conducted on human HL60 leukemic cells. Cells were exposed to sinusoidal 50 Hz EMFs at 10 μT or 1 mT for 20 min, 1 h, 24 h, or 72 h. Exposure was performed either immediately after refeeding or 1.5 h after refeeding. C‐myc transcript values were assessed by Northern blot analysis and normalized to those of the noninducible gene GaPDH. No statistically significant difference between the c‐myc transcript levels of control and exposed cells was found in lymphoid or leukemic cells under our experimental conditions, either after short exposures of 20 min and 1 h or after longer exposures of 24 and 72 h. Other experiments were carried out with pseudosynchronized cells in an attempt to establish whether cells were especially sensitive to 50 Hz magnetic field exposure in any particular phase of the cell cycle. Accordingly, cells were pseudosynchronized in G0/G1 by serum deprivation and exposed for 20 min to a 50 Hz magnetic field, at 10 μT for lymphoid cells and 1 mT for HL60 cells. No significant difference was observed between the c‐myc transcript levels of control and exposed cells for either of the synchronized cell types. These results for synchronized cells correlated with those for nonsynchronized cells. © 1995 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/bem.2250160502 |
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Viral injury to such cells makes them a good model for exploring the possible cancer‐promoting effects of 50 Hz magnetic fields. Parallel experiments were conducted on human HL60 leukemic cells. Cells were exposed to sinusoidal 50 Hz EMFs at 10 μT or 1 mT for 20 min, 1 h, 24 h, or 72 h. Exposure was performed either immediately after refeeding or 1.5 h after refeeding. C‐myc transcript values were assessed by Northern blot analysis and normalized to those of the noninducible gene GaPDH. No statistically significant difference between the c‐myc transcript levels of control and exposed cells was found in lymphoid or leukemic cells under our experimental conditions, either after short exposures of 20 min and 1 h or after longer exposures of 24 and 72 h. Other experiments were carried out with pseudosynchronized cells in an attempt to establish whether cells were especially sensitive to 50 Hz magnetic field exposure in any particular phase of the cell cycle. Accordingly, cells were pseudosynchronized in G0/G1 by serum deprivation and exposed for 20 min to a 50 Hz magnetic field, at 10 μT for lymphoid cells and 1 mT for HL60 cells. No significant difference was observed between the c‐myc transcript levels of control and exposed cells for either of the synchronized cell types. These results for synchronized cells correlated with those for nonsynchronized cells. © 1995 Wiley‐Liss, Inc.</description><identifier>ISSN: 0197-8462</identifier><identifier>EISSN: 1521-186X</identifier><identifier>DOI: 10.1002/bem.2250160502</identifier><identifier>PMID: 8554627</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>ANIMAL CELLS ; BIOLOGICAL EFFECTS ; BIOLOGY AND MEDICINE, APPLIED STUDIES ; Blotting, Northern ; c-myc oncogene ; Cell Cycle - radiation effects ; Cell Division - genetics ; Cell Division - radiation effects ; CELL PROLIFERATION ; Cell Transformation, Neoplastic - genetics ; Cell Transformation, Viral ; Cells, Cultured ; Cytological Techniques ; EBV-immortalized lymphoid cells ; ELECTROMAGNETIC FIELDS ; G1 Phase - radiation effects ; Gene Expression Regulation - radiation effects ; Gene Expression Regulation, Neoplastic - radiation effects ; GENE REGULATION ; Genes, myc - genetics ; Genes, myc - radiation effects ; Glyceraldehyde-3-Phosphate Dehydrogenases - genetics ; Glyceraldehyde-3-Phosphate Dehydrogenases - radiation effects ; Herpesvirus 4, Human ; HL60 leukemic cells ; Humans ; LEUKEMIA ; Leukemia - genetics ; Lymphoid Tissue - metabolism ; Lymphoid Tissue - radiation effects ; Lymphoid Tissue - virology ; Magnetics ; MAN ; ONCOGENES ; Proto-Oncogene Proteins c-myc - genetics ; Proto-Oncogene Proteins c-myc - radiation effects ; Resting Phase, Cell Cycle - radiation effects ; synchronized cells ; TRANSCRIPTION ; Transcription, Genetic - genetics ; Transcription, Genetic - radiation effects ; TUMOR CELLS ; Tumor Cells, Cultured</subject><ispartof>Bioelectromagnetics, 1995, Vol.16 (5), p.277-283</ispartof><rights>Copyright © 1995 Wiley‐Liss, Inc., A Wiley Company</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5122-7a264e835a24f16f46015277db22b72241d1438252a3790971c0734b815836c23</citedby><cites>FETCH-LOGICAL-c5122-7a264e835a24f16f46015277db22b72241d1438252a3790971c0734b815836c23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fbem.2250160502$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fbem.2250160502$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,882,1412,4010,27904,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8554627$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/128803$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Desjobert, Hélène</creatorcontrib><creatorcontrib>Hillion, Josette</creatorcontrib><creatorcontrib>Adolphe, Monique</creatorcontrib><creatorcontrib>Averlant, Geneviève</creatorcontrib><creatorcontrib>Nafziger, Joëlle</creatorcontrib><title>Effects of 50 Hz magnetic fields on C-myc transcript levels in nonsynchronized and synchronized human cells</title><title>Bioelectromagnetics</title><addtitle>Bioelectromagnetics</addtitle><description>The effects of 50 Hz electromagnetic fields (EMFs) on the expression of the c‐myc oncogene, known to be involved in normal cell proliferation and possibly also in tumor processes, were investigated in nonsynchronized human lymphoid cells immortalized by Epstein‐Barr virus. Viral injury to such cells makes them a good model for exploring the possible cancer‐promoting effects of 50 Hz magnetic fields. Parallel experiments were conducted on human HL60 leukemic cells. Cells were exposed to sinusoidal 50 Hz EMFs at 10 μT or 1 mT for 20 min, 1 h, 24 h, or 72 h. Exposure was performed either immediately after refeeding or 1.5 h after refeeding. C‐myc transcript values were assessed by Northern blot analysis and normalized to those of the noninducible gene GaPDH. No statistically significant difference between the c‐myc transcript levels of control and exposed cells was found in lymphoid or leukemic cells under our experimental conditions, either after short exposures of 20 min and 1 h or after longer exposures of 24 and 72 h. Other experiments were carried out with pseudosynchronized cells in an attempt to establish whether cells were especially sensitive to 50 Hz magnetic field exposure in any particular phase of the cell cycle. Accordingly, cells were pseudosynchronized in G0/G1 by serum deprivation and exposed for 20 min to a 50 Hz magnetic field, at 10 μT for lymphoid cells and 1 mT for HL60 cells. No significant difference was observed between the c‐myc transcript levels of control and exposed cells for either of the synchronized cell types. These results for synchronized cells correlated with those for nonsynchronized cells. © 1995 Wiley‐Liss, Inc.</description><subject>ANIMAL CELLS</subject><subject>BIOLOGICAL EFFECTS</subject><subject>BIOLOGY AND MEDICINE, APPLIED STUDIES</subject><subject>Blotting, Northern</subject><subject>c-myc oncogene</subject><subject>Cell Cycle - radiation effects</subject><subject>Cell Division - genetics</subject><subject>Cell Division - radiation effects</subject><subject>CELL PROLIFERATION</subject><subject>Cell Transformation, Neoplastic - genetics</subject><subject>Cell Transformation, Viral</subject><subject>Cells, Cultured</subject><subject>Cytological Techniques</subject><subject>EBV-immortalized lymphoid cells</subject><subject>ELECTROMAGNETIC FIELDS</subject><subject>G1 Phase - radiation effects</subject><subject>Gene Expression Regulation - radiation effects</subject><subject>Gene Expression Regulation, Neoplastic - radiation effects</subject><subject>GENE REGULATION</subject><subject>Genes, myc - genetics</subject><subject>Genes, myc - radiation effects</subject><subject>Glyceraldehyde-3-Phosphate Dehydrogenases - genetics</subject><subject>Glyceraldehyde-3-Phosphate Dehydrogenases - radiation effects</subject><subject>Herpesvirus 4, Human</subject><subject>HL60 leukemic cells</subject><subject>Humans</subject><subject>LEUKEMIA</subject><subject>Leukemia - genetics</subject><subject>Lymphoid Tissue - metabolism</subject><subject>Lymphoid Tissue - radiation effects</subject><subject>Lymphoid Tissue - virology</subject><subject>Magnetics</subject><subject>MAN</subject><subject>ONCOGENES</subject><subject>Proto-Oncogene Proteins c-myc - genetics</subject><subject>Proto-Oncogene Proteins c-myc - radiation effects</subject><subject>Resting Phase, Cell Cycle - radiation effects</subject><subject>synchronized cells</subject><subject>TRANSCRIPTION</subject><subject>Transcription, Genetic - genetics</subject><subject>Transcription, Genetic - radiation effects</subject><subject>TUMOR CELLS</subject><subject>Tumor Cells, Cultured</subject><issn>0197-8462</issn><issn>1521-186X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUc9P2zAUtqZNUGDX3SZ5l93S2c9x7BxZVwqibNK0id0sx3GoIXE6Ox2Uvx5XqUCc9i5Pet8Pvfc-hD5QMqWEwJfKdlMATmhBOIE3aEI50IzK4s9bNCG0FJnMCzhERzHeEkKkJOwAHUjO01RM0N28aawZIu4bzAk-f8SdvvF2cAY3zrZ1AjyeZd3W4CFoH01w6wG39p9tI3Ye-97HrTer0Hv3aGusfY1fDVabTntsbNvGE_Su0W207_f9GP0-m_-anWfLH4uL2ekyM5wCZEJDkVvJuIa8oUWTFyTdJERdAVQCIKc1zZkEDpqJkpSCGiJYXknKJSsMsGP0afTt4-BUNG6wZmV679OhisLuBYnzeeSsQ_93Y-OgOhd3W2pv-01UIhUv5c5sOhJN6GMMtlHr4DodtooStUtApQTUSwJJ8HHvvKk6Wz_T9y9PeDni96612_-4qa_zq1fe2ah1cbAPz1od7lQhmODq-vtCUXl9-W0pFuonewLcZp8O</recordid><startdate>1995</startdate><enddate>1995</enddate><creator>Desjobert, Hélène</creator><creator>Hillion, Josette</creator><creator>Adolphe, Monique</creator><creator>Averlant, Geneviève</creator><creator>Nafziger, Joëlle</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>OTOTI</scope></search><sort><creationdate>1995</creationdate><title>Effects of 50 Hz magnetic fields on C-myc transcript levels in nonsynchronized and synchronized human cells</title><author>Desjobert, Hélène ; Hillion, Josette ; Adolphe, Monique ; Averlant, Geneviève ; Nafziger, Joëlle</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5122-7a264e835a24f16f46015277db22b72241d1438252a3790971c0734b815836c23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>ANIMAL CELLS</topic><topic>BIOLOGICAL EFFECTS</topic><topic>BIOLOGY AND MEDICINE, APPLIED STUDIES</topic><topic>Blotting, Northern</topic><topic>c-myc oncogene</topic><topic>Cell Cycle - radiation effects</topic><topic>Cell Division - genetics</topic><topic>Cell Division - radiation effects</topic><topic>CELL PROLIFERATION</topic><topic>Cell Transformation, Neoplastic - genetics</topic><topic>Cell Transformation, Viral</topic><topic>Cells, Cultured</topic><topic>Cytological Techniques</topic><topic>EBV-immortalized lymphoid cells</topic><topic>ELECTROMAGNETIC FIELDS</topic><topic>G1 Phase - radiation effects</topic><topic>Gene Expression Regulation - radiation effects</topic><topic>Gene Expression Regulation, Neoplastic - radiation effects</topic><topic>GENE REGULATION</topic><topic>Genes, myc - genetics</topic><topic>Genes, myc - radiation effects</topic><topic>Glyceraldehyde-3-Phosphate Dehydrogenases - genetics</topic><topic>Glyceraldehyde-3-Phosphate Dehydrogenases - radiation effects</topic><topic>Herpesvirus 4, Human</topic><topic>HL60 leukemic cells</topic><topic>Humans</topic><topic>LEUKEMIA</topic><topic>Leukemia - genetics</topic><topic>Lymphoid Tissue - metabolism</topic><topic>Lymphoid Tissue - radiation effects</topic><topic>Lymphoid Tissue - virology</topic><topic>Magnetics</topic><topic>MAN</topic><topic>ONCOGENES</topic><topic>Proto-Oncogene Proteins c-myc - genetics</topic><topic>Proto-Oncogene Proteins c-myc - radiation effects</topic><topic>Resting Phase, Cell Cycle - radiation effects</topic><topic>synchronized cells</topic><topic>TRANSCRIPTION</topic><topic>Transcription, Genetic - genetics</topic><topic>Transcription, Genetic - radiation effects</topic><topic>TUMOR CELLS</topic><topic>Tumor Cells, Cultured</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Desjobert, Hélène</creatorcontrib><creatorcontrib>Hillion, Josette</creatorcontrib><creatorcontrib>Adolphe, Monique</creatorcontrib><creatorcontrib>Averlant, Geneviève</creatorcontrib><creatorcontrib>Nafziger, Joëlle</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>OSTI.GOV</collection><jtitle>Bioelectromagnetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Desjobert, Hélène</au><au>Hillion, Josette</au><au>Adolphe, Monique</au><au>Averlant, Geneviève</au><au>Nafziger, Joëlle</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of 50 Hz magnetic fields on C-myc transcript levels in nonsynchronized and synchronized human cells</atitle><jtitle>Bioelectromagnetics</jtitle><addtitle>Bioelectromagnetics</addtitle><date>1995</date><risdate>1995</risdate><volume>16</volume><issue>5</issue><spage>277</spage><epage>283</epage><pages>277-283</pages><issn>0197-8462</issn><eissn>1521-186X</eissn><abstract>The effects of 50 Hz electromagnetic fields (EMFs) on the expression of the c‐myc oncogene, known to be involved in normal cell proliferation and possibly also in tumor processes, were investigated in nonsynchronized human lymphoid cells immortalized by Epstein‐Barr virus. Viral injury to such cells makes them a good model for exploring the possible cancer‐promoting effects of 50 Hz magnetic fields. Parallel experiments were conducted on human HL60 leukemic cells. Cells were exposed to sinusoidal 50 Hz EMFs at 10 μT or 1 mT for 20 min, 1 h, 24 h, or 72 h. Exposure was performed either immediately after refeeding or 1.5 h after refeeding. C‐myc transcript values were assessed by Northern blot analysis and normalized to those of the noninducible gene GaPDH. No statistically significant difference between the c‐myc transcript levels of control and exposed cells was found in lymphoid or leukemic cells under our experimental conditions, either after short exposures of 20 min and 1 h or after longer exposures of 24 and 72 h. Other experiments were carried out with pseudosynchronized cells in an attempt to establish whether cells were especially sensitive to 50 Hz magnetic field exposure in any particular phase of the cell cycle. Accordingly, cells were pseudosynchronized in G0/G1 by serum deprivation and exposed for 20 min to a 50 Hz magnetic field, at 10 μT for lymphoid cells and 1 mT for HL60 cells. No significant difference was observed between the c‐myc transcript levels of control and exposed cells for either of the synchronized cell types. These results for synchronized cells correlated with those for nonsynchronized cells. © 1995 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>8554627</pmid><doi>10.1002/bem.2250160502</doi><tpages>7</tpages></addata></record> |
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subjects | ANIMAL CELLS BIOLOGICAL EFFECTS BIOLOGY AND MEDICINE, APPLIED STUDIES Blotting, Northern c-myc oncogene Cell Cycle - radiation effects Cell Division - genetics Cell Division - radiation effects CELL PROLIFERATION Cell Transformation, Neoplastic - genetics Cell Transformation, Viral Cells, Cultured Cytological Techniques EBV-immortalized lymphoid cells ELECTROMAGNETIC FIELDS G1 Phase - radiation effects Gene Expression Regulation - radiation effects Gene Expression Regulation, Neoplastic - radiation effects GENE REGULATION Genes, myc - genetics Genes, myc - radiation effects Glyceraldehyde-3-Phosphate Dehydrogenases - genetics Glyceraldehyde-3-Phosphate Dehydrogenases - radiation effects Herpesvirus 4, Human HL60 leukemic cells Humans LEUKEMIA Leukemia - genetics Lymphoid Tissue - metabolism Lymphoid Tissue - radiation effects Lymphoid Tissue - virology Magnetics MAN ONCOGENES Proto-Oncogene Proteins c-myc - genetics Proto-Oncogene Proteins c-myc - radiation effects Resting Phase, Cell Cycle - radiation effects synchronized cells TRANSCRIPTION Transcription, Genetic - genetics Transcription, Genetic - radiation effects TUMOR CELLS Tumor Cells, Cultured |
title | Effects of 50 Hz magnetic fields on C-myc transcript levels in nonsynchronized and synchronized human cells |
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