Temporal changes in the mutant frequency and mutation spectra of the 61st codon of the H-ras oncogene following exposure of B6C3F1 mice to N-nitrosodiethylamine (DEN)
Hepatocellular tumors were Induced in 15 day old male B6C3F1 mice following a single exposure to N-nitrosodiethylamine (DEN; 5 mg/kg, i.p.). Tumors were collected at 38 and 65 weeks to compare the frequencies and types of mutations in the 61st codon of the H-ras oncogene. The 61st codon was amplifie...
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Veröffentlicht in: | Carcinogenesis (New York) 1992-07, Vol.13 (7), p.1277-1279 |
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creator | Richardson, Katherine K. Rexroat, Marcia A. Helvering, Leah M. Copple, Deborah M. Richardson, Frank C. |
description | Hepatocellular tumors were Induced in 15 day old male B6C3F1 mice following a single exposure to N-nitrosodiethylamine (DEN; 5 mg/kg, i.p.). Tumors were collected at 38 and 65 weeks to compare the frequencies and types of mutations in the 61st codon of the H-ras oncogene. The 61st codon was amplified using the polymerase chain reaction (PCR). Allele-specifk oligonucleotide (ASO) probes were used to determine the frequency and types of mutations present in these tumors. Forty-nine nodular hepatic lesions were obtained from seven animals at the 38 week timepoint. Five of these samples (10%) had mutations at the 61st codon with one CAA-AAA, one CAA-CGA and three CAA-CTA. Thirty-six nodular hepatic lesions were obtained from six animals at the 65 week timepoint. Ten of these samples (28%) had mutations at the 61st codon with one CAA-AAA, five CAA-CGA and four CAA-CTA. These data indicate that DEN-induced mutations at the 61st codon of the mouse rims oncogene (i) are an infrequent event, (ii) have different frequencies at the 38 and 65 week timepoints and (iii) are different from the types of mutations seen in spontaneous lesions. |
doi_str_mv | 10.1093/carcin/13.7.1277 |
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Tumors were collected at 38 and 65 weeks to compare the frequencies and types of mutations in the 61st codon of the H-ras oncogene. The 61st codon was amplified using the polymerase chain reaction (PCR). Allele-specifk oligonucleotide (ASO) probes were used to determine the frequency and types of mutations present in these tumors. Forty-nine nodular hepatic lesions were obtained from seven animals at the 38 week timepoint. Five of these samples (10%) had mutations at the 61st codon with one CAA-AAA, one CAA-CGA and three CAA-CTA. Thirty-six nodular hepatic lesions were obtained from six animals at the 65 week timepoint. Ten of these samples (28%) had mutations at the 61st codon with one CAA-AAA, five CAA-CGA and four CAA-CTA. These data indicate that DEN-induced mutations at the 61st codon of the mouse rims oncogene (i) are an infrequent event, (ii) have different frequencies at the 38 and 65 week timepoints and (iii) are different from the types of mutations seen in spontaneous lesions.</description><identifier>ISSN: 0143-3334</identifier><identifier>EISSN: 1460-2180</identifier><identifier>DOI: 10.1093/carcin/13.7.1277</identifier><identifier>PMID: 1638698</identifier><identifier>CODEN: CRNGDP</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Alleles ; Animal tumors. Experimental tumors ; Animals ; Base Sequence ; Biological and medical sciences ; Codon - drug effects ; Diethylnitrosamine - toxicity ; DNA - genetics ; DNA - isolation & purification ; Experimental digestive system and abdominal tumors ; Genes, ras - drug effects ; Liver - drug effects ; Liver - pathology ; Liver Neoplasms - chemically induced ; Liver Neoplasms - genetics ; Liver Neoplasms - pathology ; Male ; Medical sciences ; Mice ; Mice, Inbred Strains ; Molecular Sequence Data ; Mutation ; Oligonucleotide Probes ; Time Factors ; Tumors</subject><ispartof>Carcinogenesis (New York), 1992-07, Vol.13 (7), p.1277-1279</ispartof><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c392t-55822f84cf8d76398b37d70366fb72175584b5394a459a281c1acee02cb8fc163</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5450837$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1638698$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Richardson, Katherine K.</creatorcontrib><creatorcontrib>Rexroat, Marcia A.</creatorcontrib><creatorcontrib>Helvering, Leah M.</creatorcontrib><creatorcontrib>Copple, Deborah M.</creatorcontrib><creatorcontrib>Richardson, Frank C.</creatorcontrib><title>Temporal changes in the mutant frequency and mutation spectra of the 61st codon of the H-ras oncogene following exposure of B6C3F1 mice to N-nitrosodiethylamine (DEN)</title><title>Carcinogenesis (New York)</title><addtitle>Carcinogenesis</addtitle><description>Hepatocellular tumors were Induced in 15 day old male B6C3F1 mice following a single exposure to N-nitrosodiethylamine (DEN; 5 mg/kg, i.p.). Tumors were collected at 38 and 65 weeks to compare the frequencies and types of mutations in the 61st codon of the H-ras oncogene. The 61st codon was amplified using the polymerase chain reaction (PCR). Allele-specifk oligonucleotide (ASO) probes were used to determine the frequency and types of mutations present in these tumors. Forty-nine nodular hepatic lesions were obtained from seven animals at the 38 week timepoint. Five of these samples (10%) had mutations at the 61st codon with one CAA-AAA, one CAA-CGA and three CAA-CTA. Thirty-six nodular hepatic lesions were obtained from six animals at the 65 week timepoint. Ten of these samples (28%) had mutations at the 61st codon with one CAA-AAA, five CAA-CGA and four CAA-CTA. These data indicate that DEN-induced mutations at the 61st codon of the mouse rims oncogene (i) are an infrequent event, (ii) have different frequencies at the 38 and 65 week timepoints and (iii) are different from the types of mutations seen in spontaneous lesions.</description><subject>Alleles</subject><subject>Animal tumors. Experimental tumors</subject><subject>Animals</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Codon - drug effects</subject><subject>Diethylnitrosamine - toxicity</subject><subject>DNA - genetics</subject><subject>DNA - isolation & purification</subject><subject>Experimental digestive system and abdominal tumors</subject><subject>Genes, ras - drug effects</subject><subject>Liver - drug effects</subject><subject>Liver - pathology</subject><subject>Liver Neoplasms - chemically induced</subject><subject>Liver Neoplasms - genetics</subject><subject>Liver Neoplasms - pathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred Strains</subject><subject>Molecular Sequence Data</subject><subject>Mutation</subject><subject>Oligonucleotide Probes</subject><subject>Time Factors</subject><subject>Tumors</subject><issn>0143-3334</issn><issn>1460-2180</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkUFv1DAUhCMEKtvCnQuSDwjBIVs7dmznCEvbRVqKEEWquFiOY-8aEjvYjtr9Q_xOvM2qnJ705puRn6coXiG4RLDB50oGZd05wku2RBVjT4oFIhSWFeLwabGAiOASY0yeF6cx_oIQUVw3J8VJnpw2fFH8vdHD6IPsgdpJt9URWAfSToNhStIlYIL-M2mn9kC67mGZrHcgjlqlIIE3DzBFMQHlu6wcN-syyAi8U36rnQbG972_s24L9P3o4xT0AfxIV_gSgcEqDZIH16WzKfjoO6vTbt_LwWbru08X1-9fFM-M7KN-eZxnxY_Li5vVutx8vfq8-rApFW6qVNY1ryrDiTK8YxQ3vMWsYxBTalpWIZZ10ta4IZLUjaw4UkgqrWGlWm5U_pSz4u2cOwaf745JDDYq3ffSaT9FgSinmDQwg3AGVX5wDNqIMdhBhr1AUByqEXM1AmHBxKGabHl9zJ7aQXf_DXMXWX9z1GVUsjdBOmXjI1aTGnJ8iClnzMak7x9lGX4LyjCrxfr2p7j6jjbfNuRWfMH_ADoFqAU</recordid><startdate>19920701</startdate><enddate>19920701</enddate><creator>Richardson, Katherine K.</creator><creator>Rexroat, Marcia A.</creator><creator>Helvering, Leah M.</creator><creator>Copple, Deborah M.</creator><creator>Richardson, Frank C.</creator><general>Oxford University Press</general><scope>BSCLL</scope><scope>IQODW</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>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>19920701</creationdate><title>Temporal changes in the mutant frequency and mutation spectra of the 61st codon of the H-ras oncogene following exposure of B6C3F1 mice to N-nitrosodiethylamine (DEN)</title><author>Richardson, Katherine K. ; Rexroat, Marcia A. ; Helvering, Leah M. ; Copple, Deborah M. ; Richardson, Frank C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c392t-55822f84cf8d76398b37d70366fb72175584b5394a459a281c1acee02cb8fc163</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Alleles</topic><topic>Animal tumors. Experimental tumors</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Codon - drug effects</topic><topic>Diethylnitrosamine - toxicity</topic><topic>DNA - genetics</topic><topic>DNA - isolation & purification</topic><topic>Experimental digestive system and abdominal tumors</topic><topic>Genes, ras - drug effects</topic><topic>Liver - drug effects</topic><topic>Liver - pathology</topic><topic>Liver Neoplasms - chemically induced</topic><topic>Liver Neoplasms - genetics</topic><topic>Liver Neoplasms - pathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred Strains</topic><topic>Molecular Sequence Data</topic><topic>Mutation</topic><topic>Oligonucleotide Probes</topic><topic>Time Factors</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Richardson, Katherine K.</creatorcontrib><creatorcontrib>Rexroat, Marcia A.</creatorcontrib><creatorcontrib>Helvering, Leah M.</creatorcontrib><creatorcontrib>Copple, Deborah M.</creatorcontrib><creatorcontrib>Richardson, Frank C.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Carcinogenesis (New York)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Richardson, Katherine K.</au><au>Rexroat, Marcia A.</au><au>Helvering, Leah M.</au><au>Copple, Deborah M.</au><au>Richardson, Frank C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Temporal changes in the mutant frequency and mutation spectra of the 61st codon of the H-ras oncogene following exposure of B6C3F1 mice to N-nitrosodiethylamine (DEN)</atitle><jtitle>Carcinogenesis (New York)</jtitle><addtitle>Carcinogenesis</addtitle><date>1992-07-01</date><risdate>1992</risdate><volume>13</volume><issue>7</issue><spage>1277</spage><epage>1279</epage><pages>1277-1279</pages><issn>0143-3334</issn><eissn>1460-2180</eissn><coden>CRNGDP</coden><abstract>Hepatocellular tumors were Induced in 15 day old male B6C3F1 mice following a single exposure to N-nitrosodiethylamine (DEN; 5 mg/kg, i.p.). Tumors were collected at 38 and 65 weeks to compare the frequencies and types of mutations in the 61st codon of the H-ras oncogene. The 61st codon was amplified using the polymerase chain reaction (PCR). Allele-specifk oligonucleotide (ASO) probes were used to determine the frequency and types of mutations present in these tumors. Forty-nine nodular hepatic lesions were obtained from seven animals at the 38 week timepoint. Five of these samples (10%) had mutations at the 61st codon with one CAA-AAA, one CAA-CGA and three CAA-CTA. Thirty-six nodular hepatic lesions were obtained from six animals at the 65 week timepoint. Ten of these samples (28%) had mutations at the 61st codon with one CAA-AAA, five CAA-CGA and four CAA-CTA. These data indicate that DEN-induced mutations at the 61st codon of the mouse rims oncogene (i) are an infrequent event, (ii) have different frequencies at the 38 and 65 week timepoints and (iii) are different from the types of mutations seen in spontaneous lesions.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>1638698</pmid><doi>10.1093/carcin/13.7.1277</doi><tpages>3</tpages></addata></record> |
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subjects | Alleles Animal tumors. Experimental tumors Animals Base Sequence Biological and medical sciences Codon - drug effects Diethylnitrosamine - toxicity DNA - genetics DNA - isolation & purification Experimental digestive system and abdominal tumors Genes, ras - drug effects Liver - drug effects Liver - pathology Liver Neoplasms - chemically induced Liver Neoplasms - genetics Liver Neoplasms - pathology Male Medical sciences Mice Mice, Inbred Strains Molecular Sequence Data Mutation Oligonucleotide Probes Time Factors Tumors |
title | Temporal changes in the mutant frequency and mutation spectra of the 61st codon of the H-ras oncogene following exposure of B6C3F1 mice to N-nitrosodiethylamine (DEN) |
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