Radiation-Induced Cell Transformation: Transformation Efficiencies of Different Types of Ionizing Radiation and Molecular Changes in Radiation Transformants and Tumor Cell Lines
This study aims to compare the efficiencies of 5.4 keV soft X-rays, α-particles, and γ-rays in transforming C3H 10T1/2 cells and to assess the sequence of cellular and molecular changes during the process of radiation-induced transformation of Syrian hamster embryo (SHE) cells. The somewhat more den...
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description | This study aims to compare the efficiencies of 5.4 keV soft X-rays, α-particles, and γ-rays in transforming C3H 10T1/2 cells and to assess the sequence of cellular and molecular changes during the process of radiation-induced transformation of Syrian hamster embryo (SHE) cells. The somewhat more densely ionizing soft X-rays are more effective than γ-rays both for cell inactivation and cell transformation. The relative biological effectiveness (RBE) appears to be independent of dose; it is approximately 1.3 for either end point. The RBE of α-particles versus γ-rays, on the other hand, increases with decreasing dose; the dose dependence is somewhat more apparent for cell transformation than for cell inactivation. SHE cells transformed by different types of ionizing radiation and related tumor cell lines isolated from nude mice tumors were found to have a distinct growth advantage compared to primary SHE cells, documented by higher plating efficiencies, shorter doubling times, and higher cloning efficiencies in semisolid medium. Most transformed and tumor cell lines that were investigated have elevated mRNA levels for the H-ras gene, some of them show restriction fragment length polymorphisms of the H-ras gene, and some exhibit a substantially amplified c-myc gene. In a sequence analysis of the Syrian hamster H-ras gene of eight tumor cell lines from radiation transformants, we have not found any mutation in codons 12, 13, 59, 61, nor in the flanking regions of these codons. The transformed and tumor cell lines tend to have lower chromosome numbers than primary SHE cells. |
doi_str_mv | 10.1289/ehp.9088169 |
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M.</creator><creatorcontrib>Hieber, L. ; Trutschler, K. ; Smida, J. ; Wachsmann, M. ; Ponsel, G. ; Kellerer, A. M.</creatorcontrib><description>This study aims to compare the efficiencies of 5.4 keV soft X-rays, α-particles, and γ-rays in transforming C3H 10T1/2 cells and to assess the sequence of cellular and molecular changes during the process of radiation-induced transformation of Syrian hamster embryo (SHE) cells. The somewhat more densely ionizing soft X-rays are more effective than γ-rays both for cell inactivation and cell transformation. The relative biological effectiveness (RBE) appears to be independent of dose; it is approximately 1.3 for either end point. The RBE of α-particles versus γ-rays, on the other hand, increases with decreasing dose; the dose dependence is somewhat more apparent for cell transformation than for cell inactivation. SHE cells transformed by different types of ionizing radiation and related tumor cell lines isolated from nude mice tumors were found to have a distinct growth advantage compared to primary SHE cells, documented by higher plating efficiencies, shorter doubling times, and higher cloning efficiencies in semisolid medium. Most transformed and tumor cell lines that were investigated have elevated mRNA levels for the H-ras gene, some of them show restriction fragment length polymorphisms of the H-ras gene, and some exhibit a substantially amplified c-myc gene. In a sequence analysis of the Syrian hamster H-ras gene of eight tumor cell lines from radiation transformants, we have not found any mutation in codons 12, 13, 59, 61, nor in the flanking regions of these codons. The transformed and tumor cell lines tend to have lower chromosome numbers than primary SHE cells.</description><identifier>ISSN: 0091-6765</identifier><identifier>EISSN: 1552-9924</identifier><identifier>DOI: 10.1289/ehp.9088169</identifier><identifier>PMID: 1980244</identifier><language>eng</language><publisher>United States: National Institute of Environmental Health Sciences. National Institutes of Health. Department of Health, Education and Welfare</publisher><subject>560300 - Chemicals Metabolism & Toxicology ; ALPHA PARTICLES ; ANIMAL CELLS ; Animals ; BETA DECAY RADIOISOTOPES ; BETA-MINUS DECAY RADIOISOTOPES ; Cell culture techniques ; Cell Line, Transformed ; Cell lines ; Cell Transformation, Neoplastic ; CELL TRANSFORMATIONS ; CHARGED PARTICLES ; Codons ; DAYS LIVING RADIOISOTOPES ; DOSE-RESPONSE RELATIONSHIPS ; ELECTROMAGNETIC RADIATION ; EMBRYONIC CELLS ; GAMMA RADIATION ; Gamma Rays ; GENE AMPLIFICATION ; GENE MUTATIONS ; GENES ; Genes, myc ; Genes, ras ; INACTIVATION ; IONIZING RADIATIONS ; ISOTOPES ; LIGHT NUCLEI ; MESSENGER-RNA ; Molecular and Cellular Aspects of Transformation and Differentiation ; Mutation ; MUTATIONS ; Neoplastic cell transformation ; NUCLEI ; NUCLEIC ACIDS ; ODD-ODD NUCLEI ; ONCOGENES ; ONCOGENIC TRANSFORMATIONS ; ORGANIC COMPOUNDS ; PHOSPHORUS 32 ; PHOSPHORUS ISOTOPES ; Polymorphism, Restriction Fragment Length ; RADIATION, THERMAL, AND OTHER ENVIRON. POLLUTANT EFFECTS ON LIVING ORGS. AND BIOL. MAT ; RADIATIONS ; RADIOINDUCTION ; RADIOISOTOPES ; ras genes ; RBE ; Relative Biological Effectiveness ; RFLPS ; RNA ; Transformed cell line ; Tumor cell line ; TUMOR CELLS ; Tumor Cells, Cultured ; Tumors ; X RADIATION ; X-Rays</subject><ispartof>Environmental health perspectives, 1990-08, Vol.88, p.169-174</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c463t-c98657a625a69da75a04d24fc9d4b88e35852189627facb52a7187bf98adc4ab3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/3431069$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/3431069$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,315,728,781,785,804,865,886,27929,27930,53796,53798,58022,58255</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1980244$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/5848616$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Hieber, L.</creatorcontrib><creatorcontrib>Trutschler, K.</creatorcontrib><creatorcontrib>Smida, J.</creatorcontrib><creatorcontrib>Wachsmann, M.</creatorcontrib><creatorcontrib>Ponsel, G.</creatorcontrib><creatorcontrib>Kellerer, A. M.</creatorcontrib><title>Radiation-Induced Cell Transformation: Transformation Efficiencies of Different Types of Ionizing Radiation and Molecular Changes in Radiation Transformants and Tumor Cell Lines</title><title>Environmental health perspectives</title><addtitle>Environ Health Perspect</addtitle><description>This study aims to compare the efficiencies of 5.4 keV soft X-rays, α-particles, and γ-rays in transforming C3H 10T1/2 cells and to assess the sequence of cellular and molecular changes during the process of radiation-induced transformation of Syrian hamster embryo (SHE) cells. The somewhat more densely ionizing soft X-rays are more effective than γ-rays both for cell inactivation and cell transformation. The relative biological effectiveness (RBE) appears to be independent of dose; it is approximately 1.3 for either end point. The RBE of α-particles versus γ-rays, on the other hand, increases with decreasing dose; the dose dependence is somewhat more apparent for cell transformation than for cell inactivation. SHE cells transformed by different types of ionizing radiation and related tumor cell lines isolated from nude mice tumors were found to have a distinct growth advantage compared to primary SHE cells, documented by higher plating efficiencies, shorter doubling times, and higher cloning efficiencies in semisolid medium. Most transformed and tumor cell lines that were investigated have elevated mRNA levels for the H-ras gene, some of them show restriction fragment length polymorphisms of the H-ras gene, and some exhibit a substantially amplified c-myc gene. In a sequence analysis of the Syrian hamster H-ras gene of eight tumor cell lines from radiation transformants, we have not found any mutation in codons 12, 13, 59, 61, nor in the flanking regions of these codons. The transformed and tumor cell lines tend to have lower chromosome numbers than primary SHE cells.</description><subject>560300 - Chemicals Metabolism & Toxicology</subject><subject>ALPHA PARTICLES</subject><subject>ANIMAL CELLS</subject><subject>Animals</subject><subject>BETA DECAY RADIOISOTOPES</subject><subject>BETA-MINUS DECAY RADIOISOTOPES</subject><subject>Cell culture techniques</subject><subject>Cell Line, Transformed</subject><subject>Cell lines</subject><subject>Cell Transformation, Neoplastic</subject><subject>CELL TRANSFORMATIONS</subject><subject>CHARGED PARTICLES</subject><subject>Codons</subject><subject>DAYS LIVING RADIOISOTOPES</subject><subject>DOSE-RESPONSE RELATIONSHIPS</subject><subject>ELECTROMAGNETIC RADIATION</subject><subject>EMBRYONIC CELLS</subject><subject>GAMMA RADIATION</subject><subject>Gamma Rays</subject><subject>GENE AMPLIFICATION</subject><subject>GENE MUTATIONS</subject><subject>GENES</subject><subject>Genes, myc</subject><subject>Genes, ras</subject><subject>INACTIVATION</subject><subject>IONIZING RADIATIONS</subject><subject>ISOTOPES</subject><subject>LIGHT NUCLEI</subject><subject>MESSENGER-RNA</subject><subject>Molecular and Cellular Aspects of Transformation and Differentiation</subject><subject>Mutation</subject><subject>MUTATIONS</subject><subject>Neoplastic cell transformation</subject><subject>NUCLEI</subject><subject>NUCLEIC ACIDS</subject><subject>ODD-ODD NUCLEI</subject><subject>ONCOGENES</subject><subject>ONCOGENIC TRANSFORMATIONS</subject><subject>ORGANIC COMPOUNDS</subject><subject>PHOSPHORUS 32</subject><subject>PHOSPHORUS ISOTOPES</subject><subject>Polymorphism, Restriction Fragment Length</subject><subject>RADIATION, THERMAL, AND OTHER ENVIRON. POLLUTANT EFFECTS ON LIVING ORGS. AND BIOL. MAT</subject><subject>RADIATIONS</subject><subject>RADIOINDUCTION</subject><subject>RADIOISOTOPES</subject><subject>ras genes</subject><subject>RBE</subject><subject>Relative Biological Effectiveness</subject><subject>RFLPS</subject><subject>RNA</subject><subject>Transformed cell line</subject><subject>Tumor cell line</subject><subject>TUMOR CELLS</subject><subject>Tumor Cells, Cultured</subject><subject>Tumors</subject><subject>X RADIATION</subject><subject>X-Rays</subject><issn>0091-6765</issn><issn>1552-9924</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdklFvFCEUhYnR1LX65LMJMcaXZiowwIAPJmZt7SZrTMz6TBgGdmlmYAszJvVf-Q_Fzqbd-kAInI9z7g0XgNcYnWMi5Ae7259LJATm8glYYMZIJSWhT8ECIYkr3nD2HLzI-RohhAXnJ-AES4EIpQvw54fuvB59DNUqdJOxHVzavoebpEN2MQ132sf_zvDCOW-8DWVlGB384p2zyYYRbm7389UqBv_bhy28T4A6dPBb7K2Zep3gcqfDtrA-HCEPOWHMdw820xDTXNTaB5tfgmdO99m-Ouyn4OflxWZ5Va2_f10tP68rQ3k9VkYKzhrNCdNcdrphGtGOUGdkR1shbM0EI1hIThqnTcuIbrBoWieF7gzVbX0KPs2--6kdbGdKc0n3ap_8oNOtitqrx0rwO7WNvxRmvJESF4O3s0HMo1fZ-NGanYkhWDMqJqjgmBfo_SElxZvJ5lENPpvSrA42TllhTqWsMS3g2QyaFHNO1t1XgpH6NwaqjIE6jEGh3xwX_8DO_170d7N-nceYjq1IjRpV0xqjYvMXIFe-Fw</recordid><startdate>19900801</startdate><enddate>19900801</enddate><creator>Hieber, L.</creator><creator>Trutschler, K.</creator><creator>Smida, J.</creator><creator>Wachsmann, M.</creator><creator>Ponsel, G.</creator><creator>Kellerer, A. M.</creator><general>National Institute of Environmental Health Sciences. National Institutes of Health. Department of Health, Education and Welfare</general><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>7U7</scope><scope>C1K</scope><scope>OTOTI</scope><scope>5PM</scope></search><sort><creationdate>19900801</creationdate><title>Radiation-Induced Cell Transformation: Transformation Efficiencies of Different Types of Ionizing Radiation and Molecular Changes in Radiation Transformants and Tumor Cell Lines</title><author>Hieber, L. ; Trutschler, K. ; Smida, J. ; Wachsmann, M. ; Ponsel, G. ; Kellerer, A. M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c463t-c98657a625a69da75a04d24fc9d4b88e35852189627facb52a7187bf98adc4ab3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>560300 - Chemicals Metabolism & Toxicology</topic><topic>ALPHA PARTICLES</topic><topic>ANIMAL CELLS</topic><topic>Animals</topic><topic>BETA DECAY RADIOISOTOPES</topic><topic>BETA-MINUS DECAY RADIOISOTOPES</topic><topic>Cell culture techniques</topic><topic>Cell Line, Transformed</topic><topic>Cell lines</topic><topic>Cell Transformation, Neoplastic</topic><topic>CELL TRANSFORMATIONS</topic><topic>CHARGED PARTICLES</topic><topic>Codons</topic><topic>DAYS LIVING RADIOISOTOPES</topic><topic>DOSE-RESPONSE RELATIONSHIPS</topic><topic>ELECTROMAGNETIC RADIATION</topic><topic>EMBRYONIC CELLS</topic><topic>GAMMA RADIATION</topic><topic>Gamma Rays</topic><topic>GENE AMPLIFICATION</topic><topic>GENE MUTATIONS</topic><topic>GENES</topic><topic>Genes, myc</topic><topic>Genes, ras</topic><topic>INACTIVATION</topic><topic>IONIZING RADIATIONS</topic><topic>ISOTOPES</topic><topic>LIGHT NUCLEI</topic><topic>MESSENGER-RNA</topic><topic>Molecular and Cellular Aspects of Transformation and Differentiation</topic><topic>Mutation</topic><topic>MUTATIONS</topic><topic>Neoplastic cell transformation</topic><topic>NUCLEI</topic><topic>NUCLEIC ACIDS</topic><topic>ODD-ODD NUCLEI</topic><topic>ONCOGENES</topic><topic>ONCOGENIC TRANSFORMATIONS</topic><topic>ORGANIC COMPOUNDS</topic><topic>PHOSPHORUS 32</topic><topic>PHOSPHORUS ISOTOPES</topic><topic>Polymorphism, Restriction Fragment Length</topic><topic>RADIATION, THERMAL, AND OTHER ENVIRON. POLLUTANT EFFECTS ON LIVING ORGS. AND BIOL. MAT</topic><topic>RADIATIONS</topic><topic>RADIOINDUCTION</topic><topic>RADIOISOTOPES</topic><topic>ras genes</topic><topic>RBE</topic><topic>Relative Biological Effectiveness</topic><topic>RFLPS</topic><topic>RNA</topic><topic>Transformed cell line</topic><topic>Tumor cell line</topic><topic>TUMOR CELLS</topic><topic>Tumor Cells, Cultured</topic><topic>Tumors</topic><topic>X RADIATION</topic><topic>X-Rays</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hieber, L.</creatorcontrib><creatorcontrib>Trutschler, K.</creatorcontrib><creatorcontrib>Smida, J.</creatorcontrib><creatorcontrib>Wachsmann, M.</creatorcontrib><creatorcontrib>Ponsel, G.</creatorcontrib><creatorcontrib>Kellerer, A. 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M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Radiation-Induced Cell Transformation: Transformation Efficiencies of Different Types of Ionizing Radiation and Molecular Changes in Radiation Transformants and Tumor Cell Lines</atitle><jtitle>Environmental health perspectives</jtitle><addtitle>Environ Health Perspect</addtitle><date>1990-08-01</date><risdate>1990</risdate><volume>88</volume><spage>169</spage><epage>174</epage><pages>169-174</pages><issn>0091-6765</issn><eissn>1552-9924</eissn><abstract>This study aims to compare the efficiencies of 5.4 keV soft X-rays, α-particles, and γ-rays in transforming C3H 10T1/2 cells and to assess the sequence of cellular and molecular changes during the process of radiation-induced transformation of Syrian hamster embryo (SHE) cells. The somewhat more densely ionizing soft X-rays are more effective than γ-rays both for cell inactivation and cell transformation. The relative biological effectiveness (RBE) appears to be independent of dose; it is approximately 1.3 for either end point. The RBE of α-particles versus γ-rays, on the other hand, increases with decreasing dose; the dose dependence is somewhat more apparent for cell transformation than for cell inactivation. SHE cells transformed by different types of ionizing radiation and related tumor cell lines isolated from nude mice tumors were found to have a distinct growth advantage compared to primary SHE cells, documented by higher plating efficiencies, shorter doubling times, and higher cloning efficiencies in semisolid medium. Most transformed and tumor cell lines that were investigated have elevated mRNA levels for the H-ras gene, some of them show restriction fragment length polymorphisms of the H-ras gene, and some exhibit a substantially amplified c-myc gene. In a sequence analysis of the Syrian hamster H-ras gene of eight tumor cell lines from radiation transformants, we have not found any mutation in codons 12, 13, 59, 61, nor in the flanking regions of these codons. The transformed and tumor cell lines tend to have lower chromosome numbers than primary SHE cells.</abstract><cop>United States</cop><pub>National Institute of Environmental Health Sciences. National Institutes of Health. Department of Health, Education and Welfare</pub><pmid>1980244</pmid><doi>10.1289/ehp.9088169</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 560300 - Chemicals Metabolism & Toxicology ALPHA PARTICLES ANIMAL CELLS Animals BETA DECAY RADIOISOTOPES BETA-MINUS DECAY RADIOISOTOPES Cell culture techniques Cell Line, Transformed Cell lines Cell Transformation, Neoplastic CELL TRANSFORMATIONS CHARGED PARTICLES Codons DAYS LIVING RADIOISOTOPES DOSE-RESPONSE RELATIONSHIPS ELECTROMAGNETIC RADIATION EMBRYONIC CELLS GAMMA RADIATION Gamma Rays GENE AMPLIFICATION GENE MUTATIONS GENES Genes, myc Genes, ras INACTIVATION IONIZING RADIATIONS ISOTOPES LIGHT NUCLEI MESSENGER-RNA Molecular and Cellular Aspects of Transformation and Differentiation Mutation MUTATIONS Neoplastic cell transformation NUCLEI NUCLEIC ACIDS ODD-ODD NUCLEI ONCOGENES ONCOGENIC TRANSFORMATIONS ORGANIC COMPOUNDS PHOSPHORUS 32 PHOSPHORUS ISOTOPES Polymorphism, Restriction Fragment Length RADIATION, THERMAL, AND OTHER ENVIRON. POLLUTANT EFFECTS ON LIVING ORGS. AND BIOL. MAT RADIATIONS RADIOINDUCTION RADIOISOTOPES ras genes RBE Relative Biological Effectiveness RFLPS RNA Transformed cell line Tumor cell line TUMOR CELLS Tumor Cells, Cultured Tumors X RADIATION X-Rays |
title | Radiation-Induced Cell Transformation: Transformation Efficiencies of Different Types of Ionizing Radiation and Molecular Changes in Radiation Transformants and Tumor Cell Lines |
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