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Mutagenicity of Arsenic in Mammalian Cells: Role of Reactive Oxygen Species
Arsenite, the trivalent form of arsenic present in the environment, is a known human carcinogen that lacked mutagenic activity in bacterial and standard mammalian cell mutation assays. We show herein that when evaluated in an assay (ALcell assay), in which both intragenic and multilocus mutations ar...
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Published in: | Proceedings of the National Academy of Sciences - PNAS 1998-07, Vol.95 (14), p.8103-8107 |
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creator | Hei, Tom K. Liu, Su X. Waldren, Charles |
description | Arsenite, the trivalent form of arsenic present in the environment, is a known human carcinogen that lacked mutagenic activity in bacterial and standard mammalian cell mutation assays. We show herein that when evaluated in an assay (ALcell assay), in which both intragenic and multilocus mutations are detectable, that arsenite is in fact a strong dose-dependent mutagen and that it induces mostly large deletion mutations. Cotreatment of cells with the oxygen radical scavenger dimethyl sulfoxide significantly reduces the mutagenicity of arsenite. Thus, the carcinogenicity of arsenite can be explained at least in part by it being a mutagen that depends on reactive oxygen species for its activity. |
doi_str_mv | 10.1073/pnas.95.14.8103 |
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We show herein that when evaluated in an assay (ALcell assay), in which both intragenic and multilocus mutations are detectable, that arsenite is in fact a strong dose-dependent mutagen and that it induces mostly large deletion mutations. Cotreatment of cells with the oxygen radical scavenger dimethyl sulfoxide significantly reduces the mutagenicity of arsenite. 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Thus, the carcinogenicity of arsenite can be explained at least in part by it being a mutagen that depends on reactive oxygen species for its activity.</description><subject>Animals</subject><subject>Arsenic</subject><subject>Arsenic - toxicity</subject><subject>Arsenites</subject><subject>Biological Sciences</subject><subject>Cells</subject><subject>Cellular biology</subject><subject>CHO Cells</subject><subject>Chromosomes, Human, Pair 11</subject><subject>Cricetinae</subject><subject>Genes</subject><subject>Genetic mutation</subject><subject>Human chromosomes</subject><subject>Humans</subject><subject>Hybrid Cells</subject><subject>Life Sciences (General)</subject><subject>Mammals</subject><subject>Mutagenicity</subject><subject>Mutagenicity Tests</subject><subject>Mutagens</subject><subject>Mutation</subject><subject>Mutation - drug effects</subject><subject>Polymerase chain reaction</subject><subject>Reactive Oxygen Species</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNp9kd1rFDEUxYModa0-C6Iy-NA-zfZmkkkm4ktZrBVbClWfQyZzp2aZj3WSKd3_3oRdluqDTyGc37nccw8hryksKUh2thmMX6pySfmyosCekAUFRXPBFTwlC4BC5hUv-HPywvs1AKiygiNypETJKJcL8u16DuYOB2dd2GZjm51PPv0yN2TXpu9N58yQrbDr_MfsduwwMbdobHD3mN08bKM3-75B69C_JM9a03l8tX-Pyc-Lzz9Wl_nVzZevq_Or3AooQ45Wtm1lsSmBm5gBaCULZhSra6yFqpuWWqsqVdumaVDUgByplIY2ZUE5CnZMPu3mbua6x8biECbT6c3kejNt9Wic_lsZ3C99N97rAhRL9pO9fRp_z-iD7p23MaEZcJy9poIXEoSK4Id_wPU4T0OMFidRJkVVyAid7SA7jd5P2B72oKBTRTpVpFWpKdepouh493j9A7_vJOrv93oyHtTHA07_C-h27rqADyGSb3dkBI2Ox0ibAwcqC8FSwDc7ee3DOB0m8VLGQ_0BgJS3SA</recordid><startdate>19980707</startdate><enddate>19980707</enddate><creator>Hei, Tom K.</creator><creator>Liu, Su X.</creator><creator>Waldren, Charles</creator><general>National Academy of Sciences of the United States of America</general><general>National Acad Sciences</general><general>National Academy of Sciences</general><general>The National Academy of Sciences</general><scope>CYE</scope><scope>CYI</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>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7U7</scope><scope>5PM</scope></search><sort><creationdate>19980707</creationdate><title>Mutagenicity of Arsenic in Mammalian Cells: Role of Reactive Oxygen Species</title><author>Hei, Tom K. ; Liu, Su X. ; Waldren, Charles</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c605t-ec7ff8ced504a073018723a93bbeb69bdf1cc989bcddde6b0e4e177a1d5214e63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Animals</topic><topic>Arsenic</topic><topic>Arsenic - toxicity</topic><topic>Arsenites</topic><topic>Biological Sciences</topic><topic>Cells</topic><topic>Cellular biology</topic><topic>CHO Cells</topic><topic>Chromosomes, Human, Pair 11</topic><topic>Cricetinae</topic><topic>Genes</topic><topic>Genetic mutation</topic><topic>Human chromosomes</topic><topic>Humans</topic><topic>Hybrid Cells</topic><topic>Life Sciences (General)</topic><topic>Mammals</topic><topic>Mutagenicity</topic><topic>Mutagenicity Tests</topic><topic>Mutagens</topic><topic>Mutation</topic><topic>Mutation - drug effects</topic><topic>Polymerase chain reaction</topic><topic>Reactive Oxygen Species</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hei, Tom K.</creatorcontrib><creatorcontrib>Liu, Su X.</creatorcontrib><creatorcontrib>Waldren, Charles</creatorcontrib><collection>NASA Scientific and Technical Information</collection><collection>NASA Technical Reports Server</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Toxicology Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hei, Tom K.</au><au>Liu, Su X.</au><au>Waldren, Charles</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mutagenicity of Arsenic in Mammalian Cells: Role of Reactive Oxygen Species</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>1998-07-07</date><risdate>1998</risdate><volume>95</volume><issue>14</issue><spage>8103</spage><epage>8107</epage><pages>8103-8107</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>Arsenite, the trivalent form of arsenic present in the environment, is a known human carcinogen that lacked mutagenic activity in bacterial and standard mammalian cell mutation assays. We show herein that when evaluated in an assay (ALcell assay), in which both intragenic and multilocus mutations are detectable, that arsenite is in fact a strong dose-dependent mutagen and that it induces mostly large deletion mutations. Cotreatment of cells with the oxygen radical scavenger dimethyl sulfoxide significantly reduces the mutagenicity of arsenite. Thus, the carcinogenicity of arsenite can be explained at least in part by it being a mutagen that depends on reactive oxygen species for its activity.</abstract><cop>Legacy CDMS</cop><pub>National Academy of Sciences of the United States of America</pub><pmid>9653147</pmid><doi>10.1073/pnas.95.14.8103</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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source | JSTOR Archival Journals and Primary Sources Collection【Remote access available】; PubMed Central |
subjects | Animals Arsenic Arsenic - toxicity Arsenites Biological Sciences Cells Cellular biology CHO Cells Chromosomes, Human, Pair 11 Cricetinae Genes Genetic mutation Human chromosomes Humans Hybrid Cells Life Sciences (General) Mammals Mutagenicity Mutagenicity Tests Mutagens Mutation Mutation - drug effects Polymerase chain reaction Reactive Oxygen Species |
title | Mutagenicity of Arsenic in Mammalian Cells: Role of Reactive Oxygen Species |
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