We are upgrading the repository! A content freeze is in effect until December 11, 2024. New submissions or changes to existing items will not be allowed during this period. All content already published will remain publicly available for searching and downloading. Updates will be posted in the Website Upgrade 2024 FAQ in the sidebar Help menu. Reach out to escholarship@umassmed.edu with any questions.

Show simple item record

dc.contributor.authorFraire, Armando E.
dc.contributor.authorGreenberg, S. Donald
dc.contributor.authorSpjut, Harlan J.
dc.contributor.authorRoggli, Victor L.
dc.contributor.authorDodson, Ronald F.
dc.contributor.authorCartwright, Joiner
dc.contributor.authorWilliams, Glenn
dc.contributor.authorBaker, Stephen P.
dc.date2022-08-11T08:09:11.000
dc.date.accessioned2022-08-23T16:20:28Z
dc.date.available2022-08-23T16:20:28Z
dc.date.issued1994-08-01
dc.date.submitted2008-05-05
dc.identifier.citationAm J Respir Crit Care Med. 1994 Aug;150(2):521-7.
dc.identifier.issn1073-449X (Print)
dc.identifier.pmid8049840
dc.identifier.urihttp://hdl.handle.net/20.500.14038/35288
dc.description.abstractFemale Fisher 344 rats (n = 25) were inoculated intrapleurally with a single 20-mg dose of (JM-100) fibrous glass. The mean length (2.2 microns) and width (0.15 microns) of the fibrous glass particles was within respirable range. Following inoculation, the rats were killed at timed intervals ranging from 2 to 430 d from inoculation. The pleural histopathologic changes were independently observed by a panel of three pathologists blinded to the time elapsed from inoculation. Fibrous adhesions, nodular lesions, and grossly evident tumor were noted in 15, 2, and 1 rat, respectively. In 1 rat there were combined adhesive and nodular changes, and in 6 there were no grossly detectable abnormalities. Chronic inflammation, fibrosis, and foreign body reaction were found in 9, 18, and 10 rats, respectively. Mesothelial hyperplasia and dysplasia were observed in 16 and 9 rats, respectively. Of 16 rats with the severest degree of hyperplasia and dysplasia, 3 developed malignant mesothelioma. This study suggests that a spectrum of rat pleural mesothelial histopathologic changes occurs before development of mesothelioma. The association of severe dysplasia in 3 rats with fully developed mesothelioma suggests that there may be a gradual progression from mesothelial hyperplasia or dysplasia to mesothelioma. Multivariate analysis further suggests that gross pleural nodular lesions and dysplasia may be significantly associated with the development of mesothelioma in this experimental model.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=8049840&dopt=Abstract ">Link to article in PubMed</a>
dc.relation.urlhttp://ajrccm.atsjournals.org/content/150/2/521.long
dc.subjectAdhesions
dc.subjectAnimals
dc.subjectEpithelium
dc.subjectFemale
dc.subjectFibrosis
dc.subjectForeign-Body Reaction
dc.subject*Glass
dc.subjectInflammation
dc.subjectMesothelioma
dc.subjectPleura
dc.subjectPleural Neoplasms
dc.subjectRats
dc.subjectRats, Inbred F344
dc.subjectCancer Biology
dc.subjectCell and Developmental Biology
dc.titleEffect of fibrous glass on rat pleural mesothelium. Histopathologic observations
dc.typeJournal Article
dc.source.journaltitleAmerican journal of respiratory and critical care medicine
dc.source.volume150
dc.source.issue2
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/infoservices/33
dc.identifier.contextkey503856
html.description.abstract<p>Female Fisher 344 rats (n = 25) were inoculated intrapleurally with a single 20-mg dose of (JM-100) fibrous glass. The mean length (2.2 microns) and width (0.15 microns) of the fibrous glass particles was within respirable range. Following inoculation, the rats were killed at timed intervals ranging from 2 to 430 d from inoculation. The pleural histopathologic changes were independently observed by a panel of three pathologists blinded to the time elapsed from inoculation. Fibrous adhesions, nodular lesions, and grossly evident tumor were noted in 15, 2, and 1 rat, respectively. In 1 rat there were combined adhesive and nodular changes, and in 6 there were no grossly detectable abnormalities. Chronic inflammation, fibrosis, and foreign body reaction were found in 9, 18, and 10 rats, respectively. Mesothelial hyperplasia and dysplasia were observed in 16 and 9 rats, respectively. Of 16 rats with the severest degree of hyperplasia and dysplasia, 3 developed malignant mesothelioma. This study suggests that a spectrum of rat pleural mesothelial histopathologic changes occurs before development of mesothelioma. The association of severe dysplasia in 3 rats with fully developed mesothelioma suggests that there may be a gradual progression from mesothelial hyperplasia or dysplasia to mesothelioma. Multivariate analysis further suggests that gross pleural nodular lesions and dysplasia may be significantly associated with the development of mesothelioma in this experimental model.</p>
dc.identifier.submissionpathinfoservices/33
dc.contributor.departmentDepartment of Pathology
dc.contributor.departmentDepartment of Cell Biology
dc.contributor.departmentInformation Services, Academic Computing Services
dc.source.pages521-7


This item appears in the following Collection(s)

Show simple item record