Proliferative Lesions of the Mouse Lung: Progression Studies in Strain A Mice
The progression of pulmonary neoplasia was examined in strain A/J male mice treated with a single dose of vinyl carbamate (60 mg/kg, i.p.) 6 weeks after birth. Interim sacrifices were performed at 7, 8, 10, 12, or 14 months. Proliferative lesions of the lung were divided into four categories: hyperp...
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Veröffentlicht in: | Experimental lung research 1991-01, Vol.17 (2), p.157-168 |
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description | The progression of pulmonary neoplasia was examined in strain A/J male mice treated with a single dose of vinyl carbamate (60 mg/kg, i.p.) 6 weeks after birth. Interim sacrifices were performed at 7, 8, 10, 12, or 14 months. Proliferative lesions of the lung were divided into four categories: hyperplasias, adenomas, carcinomas arising within adenomas, and carcinomas. Grossly visible surface tumor counts, histologic diagnoses, and morphometric measurements of histologic lesions were used to evaluate progression. Vinyl carbamate-treated mice showed increased mean surface tumor counts at all time points. Diagnostic evaluation suggested that as a function of time, the relative frequency of hyperplasias decreased and the relative frequency of adenomas increased. The relative frequency of adenomas subsequently decreased, whereas the relative frequency of carcinomas increased. At all time points, carcinomas arising within adenomas were present. As time progressed, the number of carcinomas arising within adenomas decreased, whereas the number of "pure" carcinomas increased. Morphometric analysis of lesions indicated hyperplasias to be small, that adenomas were larger than hyperplasias, and carcinomas were larger than adenomas and hyperplasias, suggesting that few adenomas or carcinomas arise de novo. Collectively, these data suggest that the majority of pulmonary tumors in A/J mice treated with vinyl carbamate arise as hyperplasias, progress to adenomas, and ultimately result in carcinomas. |
doi_str_mv | 10.3109/01902149109064408 |
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Interim sacrifices were performed at 7, 8, 10, 12, or 14 months. Proliferative lesions of the lung were divided into four categories: hyperplasias, adenomas, carcinomas arising within adenomas, and carcinomas. Grossly visible surface tumor counts, histologic diagnoses, and morphometric measurements of histologic lesions were used to evaluate progression. Vinyl carbamate-treated mice showed increased mean surface tumor counts at all time points. Diagnostic evaluation suggested that as a function of time, the relative frequency of hyperplasias decreased and the relative frequency of adenomas increased. The relative frequency of adenomas subsequently decreased, whereas the relative frequency of carcinomas increased. At all time points, carcinomas arising within adenomas were present. As time progressed, the number of carcinomas arising within adenomas decreased, whereas the number of "pure" carcinomas increased. Morphometric analysis of lesions indicated hyperplasias to be small, that adenomas were larger than hyperplasias, and carcinomas were larger than adenomas and hyperplasias, suggesting that few adenomas or carcinomas arise de novo. Collectively, these data suggest that the majority of pulmonary tumors in A/J mice treated with vinyl carbamate arise as hyperplasias, progress to adenomas, and ultimately result in carcinomas.</description><identifier>ISSN: 0190-2148</identifier><identifier>EISSN: 1521-0499</identifier><identifier>DOI: 10.3109/01902149109064408</identifier><identifier>PMID: 2050022</identifier><language>eng</language><publisher>England: Informa UK Ltd</publisher><subject>Animals ; Cell Division - physiology ; Disease Models, Animal ; Lung Neoplasms - chemically induced ; Lung Neoplasms - genetics ; Lung Neoplasms - pathology ; Male ; Mice ; Mice, Inbred A ; Urethane - analogs & derivatives</subject><ispartof>Experimental lung research, 1991-01, Vol.17 (2), p.157-168</ispartof><rights>1991 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 1991</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c467t-3eca98ef4ed23ed5ebea1a6aa3779616004b01f6389ee912f0c58e2f035881b3</citedby><cites>FETCH-LOGICAL-c467t-3eca98ef4ed23ed5ebea1a6aa3779616004b01f6389ee912f0c58e2f035881b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.3109/01902149109064408$$EPDF$$P50$$Ginformaworld$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.3109/01902149109064408$$EHTML$$P50$$Ginformaworld$$H</linktohtml><link.rule.ids>314,780,784,27922,27923,59645,60434,61219,61400</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2050022$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Foley, Julie F.</creatorcontrib><creatorcontrib>Anderson, Marshall W.</creatorcontrib><creatorcontrib>Stoner, Gary D.</creatorcontrib><creatorcontrib>Gaul, Beth W.</creatorcontrib><creatorcontrib>Hardisty, Jerry F.</creatorcontrib><creatorcontrib>Maronpot, Robert R.</creatorcontrib><title>Proliferative Lesions of the Mouse Lung: Progression Studies in Strain A Mice</title><title>Experimental lung research</title><addtitle>Exp Lung Res</addtitle><description>The progression of pulmonary neoplasia was examined in strain A/J male mice treated with a single dose of vinyl carbamate (60 mg/kg, i.p.) 6 weeks after birth. Interim sacrifices were performed at 7, 8, 10, 12, or 14 months. Proliferative lesions of the lung were divided into four categories: hyperplasias, adenomas, carcinomas arising within adenomas, and carcinomas. Grossly visible surface tumor counts, histologic diagnoses, and morphometric measurements of histologic lesions were used to evaluate progression. Vinyl carbamate-treated mice showed increased mean surface tumor counts at all time points. Diagnostic evaluation suggested that as a function of time, the relative frequency of hyperplasias decreased and the relative frequency of adenomas increased. The relative frequency of adenomas subsequently decreased, whereas the relative frequency of carcinomas increased. At all time points, carcinomas arising within adenomas were present. As time progressed, the number of carcinomas arising within adenomas decreased, whereas the number of "pure" carcinomas increased. Morphometric analysis of lesions indicated hyperplasias to be small, that adenomas were larger than hyperplasias, and carcinomas were larger than adenomas and hyperplasias, suggesting that few adenomas or carcinomas arise de novo. Collectively, these data suggest that the majority of pulmonary tumors in A/J mice treated with vinyl carbamate arise as hyperplasias, progress to adenomas, and ultimately result in carcinomas.</description><subject>Animals</subject><subject>Cell Division - physiology</subject><subject>Disease Models, Animal</subject><subject>Lung Neoplasms - chemically induced</subject><subject>Lung Neoplasms - genetics</subject><subject>Lung Neoplasms - pathology</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred A</subject><subject>Urethane - analogs & derivatives</subject><issn>0190-2148</issn><issn>1521-0499</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UF1LwzAUDaLMOf0BPgj5A9WbNu0S9WUMv2BDwb2XtL3ZMrpmJK2yf2_KhiCiT-dwzweXQ8glg-uEgbwBJiFmXAYOGecgjsiQpTGLgEt5TIa9HgWDOCVn3q8BIE5FNiCDGNLA4yGZvzlbG41OteYD6Qy9sY2nVtN2hXRuOx-OXbO8pcG4dOh7nb63XWXQU9NTpwJM6NyUeE5OtKo9XhxwRBaPD4vpczR7fXqZTmZRybNxGyVYKilQc6ziBKsUC1RMZUol47HMWAbAC2A6S4RElCzWUKYCAySpEKxIRoTta0tnvXeo860zG-V2OYO8Hyb_NUzIXO0z267YYPWdOCwR9Pu9bhpt3UZ9WldXeat2tXXaqaY0vq_-u_7uR3yFqm5XpXKYr23nmrDGP899AVZrgoc</recordid><startdate>19910101</startdate><enddate>19910101</enddate><creator>Foley, Julie F.</creator><creator>Anderson, Marshall W.</creator><creator>Stoner, Gary D.</creator><creator>Gaul, Beth W.</creator><creator>Hardisty, Jerry F.</creator><creator>Maronpot, Robert R.</creator><general>Informa UK Ltd</general><general>Taylor & Francis</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></search><sort><creationdate>19910101</creationdate><title>Proliferative Lesions of the Mouse Lung: Progression Studies in Strain A Mice</title><author>Foley, Julie F. ; Anderson, Marshall W. ; Stoner, Gary D. ; Gaul, Beth W. ; Hardisty, Jerry F. ; Maronpot, Robert R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c467t-3eca98ef4ed23ed5ebea1a6aa3779616004b01f6389ee912f0c58e2f035881b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Animals</topic><topic>Cell Division - physiology</topic><topic>Disease Models, Animal</topic><topic>Lung Neoplasms - chemically induced</topic><topic>Lung Neoplasms - genetics</topic><topic>Lung Neoplasms - pathology</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred A</topic><topic>Urethane - analogs & derivatives</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Foley, Julie F.</creatorcontrib><creatorcontrib>Anderson, Marshall W.</creatorcontrib><creatorcontrib>Stoner, Gary D.</creatorcontrib><creatorcontrib>Gaul, Beth W.</creatorcontrib><creatorcontrib>Hardisty, Jerry F.</creatorcontrib><creatorcontrib>Maronpot, Robert R.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Experimental lung research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Foley, Julie F.</au><au>Anderson, Marshall W.</au><au>Stoner, Gary D.</au><au>Gaul, Beth W.</au><au>Hardisty, Jerry F.</au><au>Maronpot, Robert R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Proliferative Lesions of the Mouse Lung: Progression Studies in Strain A Mice</atitle><jtitle>Experimental lung research</jtitle><addtitle>Exp Lung Res</addtitle><date>1991-01-01</date><risdate>1991</risdate><volume>17</volume><issue>2</issue><spage>157</spage><epage>168</epage><pages>157-168</pages><issn>0190-2148</issn><eissn>1521-0499</eissn><abstract>The progression of pulmonary neoplasia was examined in strain A/J male mice treated with a single dose of vinyl carbamate (60 mg/kg, i.p.) 6 weeks after birth. Interim sacrifices were performed at 7, 8, 10, 12, or 14 months. Proliferative lesions of the lung were divided into four categories: hyperplasias, adenomas, carcinomas arising within adenomas, and carcinomas. Grossly visible surface tumor counts, histologic diagnoses, and morphometric measurements of histologic lesions were used to evaluate progression. Vinyl carbamate-treated mice showed increased mean surface tumor counts at all time points. Diagnostic evaluation suggested that as a function of time, the relative frequency of hyperplasias decreased and the relative frequency of adenomas increased. The relative frequency of adenomas subsequently decreased, whereas the relative frequency of carcinomas increased. At all time points, carcinomas arising within adenomas were present. As time progressed, the number of carcinomas arising within adenomas decreased, whereas the number of "pure" carcinomas increased. Morphometric analysis of lesions indicated hyperplasias to be small, that adenomas were larger than hyperplasias, and carcinomas were larger than adenomas and hyperplasias, suggesting that few adenomas or carcinomas arise de novo. Collectively, these data suggest that the majority of pulmonary tumors in A/J mice treated with vinyl carbamate arise as hyperplasias, progress to adenomas, and ultimately result in carcinomas.</abstract><cop>England</cop><pub>Informa UK Ltd</pub><pmid>2050022</pmid><doi>10.3109/01902149109064408</doi><tpages>12</tpages></addata></record> |
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subjects | Animals Cell Division - physiology Disease Models, Animal Lung Neoplasms - chemically induced Lung Neoplasms - genetics Lung Neoplasms - pathology Male Mice Mice, Inbred A Urethane - analogs & derivatives |
title | Proliferative Lesions of the Mouse Lung: Progression Studies in Strain A Mice |
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