Differential Dose Responses of Pulmonary Tumor Types in the Rat after Inhalation of Plutonium Dioxide Aerosols
Dose responses were compared among primary lung tumors and their histological types induced by a single inhalation exposure of female Wistar strain rats to submicron-size and polydispersed aerosols of plutonium dioxide (^^239 PuO_2 ). While the primary lung tumors were found only in 2.3% of the unex...
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description | Dose responses were compared among primary lung tumors and their histological types induced by a single inhalation exposure of female Wistar strain rats to submicron-size and polydispersed aerosols of plutonium dioxide (^^239 PuO_2 ). While the primary lung tumors were found only in 2.3% of the unexposed control animals, the frequency of all the primary lung tumors in the exposed animals was 44% at the mean lung dose of 0.71 Gy, and increased sharply at the doses of 1.5 Gy or more, reaching the maximum of 97% at 5.4 Gy, and the dose responses around at 1.0 Gy were different between benign and malignant lung tumors. Almost all the pulmonary tumors in the exposed animals were classified into epithelial types such as adenomas, adenocarcinomas, adenosquamous carcinomas, and squamous cell carcinomas. The dose responses were different between these tumor types as shown by the peak incidence of adenomas at 0.71 Gy, adenocarcinomas at 2.9 Gy, adenosquamous and squamous cell carcinomas at 5.4-8.5 Gy, respectively. As the magnitudes of neoplastic lesions in pulmonary carcinomas were expressed by histological scores, metaplasias and adenomatous lesions most frequently appeared at doses of 1.5 Gy, while the appearance and increase of carcinomatous lesions differed in the dose ranges as shown by the peak incidence of adenocarcinomatous lesions at 2.9 Gy, and adenosquamous or squamous lesions at 5.4-6.6 Gy. These results indicate a differential dose response of pulmonary carcinogenesis in which metaplasias and benign adenomas were induced at lower doses (1.5 Gy). Together with the increase of carcinomatous lesions at higher doses, the intranuclear p53 protein accumulation was detectable, but only in a few percentages of malignant carcinomas. |
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While the primary lung tumors were found only in 2.3% of the unexposed control animals, the frequency of all the primary lung tumors in the exposed animals was 44% at the mean lung dose of 0.71 Gy, and increased sharply at the doses of 1.5 Gy or more, reaching the maximum of 97% at 5.4 Gy, and the dose responses around at 1.0 Gy were different between benign and malignant lung tumors. Almost all the pulmonary tumors in the exposed animals were classified into epithelial types such as adenomas, adenocarcinomas, adenosquamous carcinomas, and squamous cell carcinomas. The dose responses were different between these tumor types as shown by the peak incidence of adenomas at 0.71 Gy, adenocarcinomas at 2.9 Gy, adenosquamous and squamous cell carcinomas at 5.4-8.5 Gy, respectively. As the magnitudes of neoplastic lesions in pulmonary carcinomas were expressed by histological scores, metaplasias and adenomatous lesions most frequently appeared at doses of 1.5 Gy, while the appearance and increase of carcinomatous lesions differed in the dose ranges as shown by the peak incidence of adenocarcinomatous lesions at 2.9 Gy, and adenosquamous or squamous lesions at 5.4-6.6 Gy. These results indicate a differential dose response of pulmonary carcinogenesis in which metaplasias and benign adenomas were induced at lower doses (<1.0 Gy), whereas malignant carcinomas were induced at relatively higher doses (>1.5 Gy). Together with the increase of carcinomatous lesions at higher doses, the intranuclear p53 protein accumulation was detectable, but only in a few percentages of malignant carcinomas.</description><identifier>ISSN: 0449-3060</identifier><identifier>EISSN: 1349-9157</identifier><identifier>DOI: 10.1269/jrr.39.61</identifier><identifier>PMID: 9610033</identifier><language>eng</language><publisher>England: THE JAPAN RADIATION RESEARCH SOCIETY</publisher><subject>Administration, Inhalation ; Aerosols ; Animals ; Comparative analysis ; Dose-Response Relationship, Radiation ; Female ; Lung cancer ; Lung Neoplasms - etiology ; Lung Neoplasms - pathology ; Neoplasms, Radiation-Induced - etiology ; Neoplasms, Radiation-Induced - pathology ; Plutonium ; Plutonium - administration & dosage ; Plutonium - toxicity ; Rats ; Rats, Wistar ; Squamous cell carcinoma ; Tumor proteins ; Tumor Suppressor Protein p53 - genetics ; Tumor Suppressor Protein p53 - metabolism ; Tumors</subject><ispartof>JOURNAL OF RADIATION RESEARCH, 1998, Vol.39 (1), p.61-72</ispartof><rights>COPYRIGHT 1998 Oxford University Press</rights><rights>Copyright Japan Science and Technology Agency 1998</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c637t-b67ca0137e8fc710ac6a7f32fb8763bf60fa5645fcd1b161ae403ae6fb93c4f73</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9610033$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Oghiso, Y</creatorcontrib><creatorcontrib>Yamada, Y</creatorcontrib><creatorcontrib>Iida, H</creatorcontrib><creatorcontrib>Inaba, J</creatorcontrib><creatorcontrib>Division of Radiotoxicology and Protection</creatorcontrib><creatorcontrib>National Institute of Radiological Sciences</creatorcontrib><title>Differential Dose Responses of Pulmonary Tumor Types in the Rat after Inhalation of Plutonium Dioxide Aerosols</title><title>JOURNAL OF RADIATION RESEARCH</title><addtitle>J Radiat Res</addtitle><description>Dose responses were compared among primary lung tumors and their histological types induced by a single inhalation exposure of female Wistar strain rats to submicron-size and polydispersed aerosols of plutonium dioxide (^^239 PuO_2 ). While the primary lung tumors were found only in 2.3% of the unexposed control animals, the frequency of all the primary lung tumors in the exposed animals was 44% at the mean lung dose of 0.71 Gy, and increased sharply at the doses of 1.5 Gy or more, reaching the maximum of 97% at 5.4 Gy, and the dose responses around at 1.0 Gy were different between benign and malignant lung tumors. Almost all the pulmonary tumors in the exposed animals were classified into epithelial types such as adenomas, adenocarcinomas, adenosquamous carcinomas, and squamous cell carcinomas. The dose responses were different between these tumor types as shown by the peak incidence of adenomas at 0.71 Gy, adenocarcinomas at 2.9 Gy, adenosquamous and squamous cell carcinomas at 5.4-8.5 Gy, respectively. As the magnitudes of neoplastic lesions in pulmonary carcinomas were expressed by histological scores, metaplasias and adenomatous lesions most frequently appeared at doses of 1.5 Gy, while the appearance and increase of carcinomatous lesions differed in the dose ranges as shown by the peak incidence of adenocarcinomatous lesions at 2.9 Gy, and adenosquamous or squamous lesions at 5.4-6.6 Gy. These results indicate a differential dose response of pulmonary carcinogenesis in which metaplasias and benign adenomas were induced at lower doses (<1.0 Gy), whereas malignant carcinomas were induced at relatively higher doses (>1.5 Gy). Together with the increase of carcinomatous lesions at higher doses, the intranuclear p53 protein accumulation was detectable, but only in a few percentages of malignant carcinomas.</description><subject>Administration, Inhalation</subject><subject>Aerosols</subject><subject>Animals</subject><subject>Comparative analysis</subject><subject>Dose-Response Relationship, Radiation</subject><subject>Female</subject><subject>Lung cancer</subject><subject>Lung Neoplasms - etiology</subject><subject>Lung Neoplasms - pathology</subject><subject>Neoplasms, Radiation-Induced - etiology</subject><subject>Neoplasms, Radiation-Induced - pathology</subject><subject>Plutonium</subject><subject>Plutonium - administration & dosage</subject><subject>Plutonium - toxicity</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Squamous cell carcinoma</subject><subject>Tumor proteins</subject><subject>Tumor Suppressor Protein p53 - genetics</subject><subject>Tumor Suppressor Protein p53 - metabolism</subject><subject>Tumors</subject><issn>0449-3060</issn><issn>1349-9157</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFUdGKUzEQDaKsZd0HP0AI-ORDa6a5N7l5LNtdXVhQpD6H3HTipuYmNckF9-9NbVHCMMOcc5LJGULeAlvBWqiPh5xXXK0EvCAL4J1aKujlS7JgXas5E-w1uSnFjwx6wdgAcEWulADGOF-QuPXOYcZYvQl0mwrSb1iOKRYsNDn6dQ5TiiY_0908pUx3z8cG-EjrU2OaSo2rmOlDfDLBVJ_iX1GYa4p-nujWp99-j3SDOZUUyhvyyplQ8OaSr8n3-7vd7efl45dPD7ebx6UVXNblKKQ1DLjEwVkJzFhhpONrNw5S8NEJ5kwvut7ZPYwgwGDHuEHhRsVt5yS_Ju_P9x5z-jVjqfqQ5hzbkxq65gtjSvHGWp1ZP0xA7aNLNRvbzh4nb1NE51t_03MBfQegmuDDWWDbd0pGp4_ZT80dDUyflqHbMjRXWkDjvruMMI8T7v8xL9Y3_P6MN9BbE1IMPuL_Oe1PcUg5owalBt0kikFL4hSnQq4FH1Qn-R-T25uZ</recordid><startdate>1998</startdate><enddate>1998</enddate><creator>Oghiso, Y</creator><creator>Yamada, Y</creator><creator>Iida, H</creator><creator>Inaba, J</creator><general>THE JAPAN RADIATION RESEARCH SOCIETY</general><general>Oxford University Press</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>K9.</scope></search><sort><creationdate>1998</creationdate><title>Differential Dose Responses of Pulmonary Tumor Types in the Rat after Inhalation of Plutonium Dioxide Aerosols</title><author>Oghiso, Y ; Yamada, Y ; Iida, H ; Inaba, J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c637t-b67ca0137e8fc710ac6a7f32fb8763bf60fa5645fcd1b161ae403ae6fb93c4f73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Administration, Inhalation</topic><topic>Aerosols</topic><topic>Animals</topic><topic>Comparative analysis</topic><topic>Dose-Response Relationship, Radiation</topic><topic>Female</topic><topic>Lung cancer</topic><topic>Lung Neoplasms - etiology</topic><topic>Lung Neoplasms - pathology</topic><topic>Neoplasms, Radiation-Induced - etiology</topic><topic>Neoplasms, Radiation-Induced - pathology</topic><topic>Plutonium</topic><topic>Plutonium - administration & dosage</topic><topic>Plutonium - toxicity</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Squamous cell carcinoma</topic><topic>Tumor proteins</topic><topic>Tumor Suppressor Protein p53 - genetics</topic><topic>Tumor Suppressor Protein p53 - metabolism</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Oghiso, Y</creatorcontrib><creatorcontrib>Yamada, Y</creatorcontrib><creatorcontrib>Iida, H</creatorcontrib><creatorcontrib>Inaba, J</creatorcontrib><creatorcontrib>Division of Radiotoxicology and Protection</creatorcontrib><creatorcontrib>National Institute of Radiological Sciences</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><jtitle>JOURNAL OF RADIATION RESEARCH</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Oghiso, Y</au><au>Yamada, Y</au><au>Iida, H</au><au>Inaba, J</au><aucorp>Division of Radiotoxicology and Protection</aucorp><aucorp>National Institute of Radiological Sciences</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential Dose Responses of Pulmonary Tumor Types in the Rat after Inhalation of Plutonium Dioxide Aerosols</atitle><jtitle>JOURNAL OF RADIATION RESEARCH</jtitle><addtitle>J Radiat Res</addtitle><date>1998</date><risdate>1998</risdate><volume>39</volume><issue>1</issue><spage>61</spage><epage>72</epage><pages>61-72</pages><issn>0449-3060</issn><eissn>1349-9157</eissn><abstract>Dose responses were compared among primary lung tumors and their histological types induced by a single inhalation exposure of female Wistar strain rats to submicron-size and polydispersed aerosols of plutonium dioxide (^^239 PuO_2 ). While the primary lung tumors were found only in 2.3% of the unexposed control animals, the frequency of all the primary lung tumors in the exposed animals was 44% at the mean lung dose of 0.71 Gy, and increased sharply at the doses of 1.5 Gy or more, reaching the maximum of 97% at 5.4 Gy, and the dose responses around at 1.0 Gy were different between benign and malignant lung tumors. Almost all the pulmonary tumors in the exposed animals were classified into epithelial types such as adenomas, adenocarcinomas, adenosquamous carcinomas, and squamous cell carcinomas. The dose responses were different between these tumor types as shown by the peak incidence of adenomas at 0.71 Gy, adenocarcinomas at 2.9 Gy, adenosquamous and squamous cell carcinomas at 5.4-8.5 Gy, respectively. As the magnitudes of neoplastic lesions in pulmonary carcinomas were expressed by histological scores, metaplasias and adenomatous lesions most frequently appeared at doses of 1.5 Gy, while the appearance and increase of carcinomatous lesions differed in the dose ranges as shown by the peak incidence of adenocarcinomatous lesions at 2.9 Gy, and adenosquamous or squamous lesions at 5.4-6.6 Gy. These results indicate a differential dose response of pulmonary carcinogenesis in which metaplasias and benign adenomas were induced at lower doses (<1.0 Gy), whereas malignant carcinomas were induced at relatively higher doses (>1.5 Gy). Together with the increase of carcinomatous lesions at higher doses, the intranuclear p53 protein accumulation was detectable, but only in a few percentages of malignant carcinomas.</abstract><cop>England</cop><pub>THE JAPAN RADIATION RESEARCH SOCIETY</pub><pmid>9610033</pmid><doi>10.1269/jrr.39.61</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Administration, Inhalation Aerosols Animals Comparative analysis Dose-Response Relationship, Radiation Female Lung cancer Lung Neoplasms - etiology Lung Neoplasms - pathology Neoplasms, Radiation-Induced - etiology Neoplasms, Radiation-Induced - pathology Plutonium Plutonium - administration & dosage Plutonium - toxicity Rats Rats, Wistar Squamous cell carcinoma Tumor proteins Tumor Suppressor Protein p53 - genetics Tumor Suppressor Protein p53 - metabolism Tumors |
title | Differential Dose Responses of Pulmonary Tumor Types in the Rat after Inhalation of Plutonium Dioxide Aerosols |
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