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A BALB/c murine lung alveolar carcinoma used to establish a surgical spontaneous metastasis model

dc.contributor.authorMcLean, Michaelen_US
dc.contributor.authorWallace, Howard L.en_US
dc.contributor.authorSharma, Atimaen_US
dc.contributor.authorHill, Hank C.en_US
dc.contributor.authorSabel, Michael S.en_US
dc.contributor.authorEgilmez, Nejat K.en_US
dc.date.accessioned2006-09-08T20:30:05Z
dc.date.available2006-09-08T20:30:05Z
dc.date.issued2004-10en_US
dc.identifier.citationMcLean, Michael; Wallace, Howard L.; Sharma, Atima; Hill, Hank C.; Sabel, Michael S.; Egilmez, Nejat K.; (2004). "A BALB/c murine lung alveolar carcinoma used to establish a surgical spontaneous metastasis model." Clinical & Experimental Metastasis 21(4): 363-369. <http://hdl.handle.net/2027.42/42586>en_US
dc.identifier.issn0262-0898en_US
dc.identifier.issn1573-7276en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/42586
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=15554393&dopt=citationen_US
dc.description.abstractLine-1, a weakly immunogenic lung tumor cell line derived from the BALB/c mouse, metastasizes spontaneously to the lungs of mice following subcutaneous administration. The parameters that influence metastasis as well as the progression of metastatic lung disease following surgical resection of primary subcutaneous tumors were characterized. Histological analysis of the lungs obtained from mice bearing different size subcutaneous tumors demonstrated that >90% of the mice developed micrometastatic disease in the lungs when the tumor exceeded 650 mm 3 in size. Surgical resection of subcutaneous tumors resulted in the cure of primary disease in 95% of the mice. Macroscopic tumor nodules were grossly visible in the lungs of 75% of the mice 5 weeks after surgery. Serum amyloid A level correlated with primary tumor burden and was diagnostic for the presence of metastatic disease. The efficiency of metastasis, post-surgical primary tumor recurrence and long-term survival were significantly different between BALB/c mice obtained from different suppliers. The Line-1-BALB/c surgical metastasis model provides a clinically relevant tool for the evaluation of anti-cancer therapies, especially those that are designed to target long-term suppression of minimal residual disease following surgical intervention.en_US
dc.format.extent289317 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherKluwer Academic Publishers; Springer Science+Business Mediaen_US
dc.subject.otherMedicine & Public Healthen_US
dc.subject.otherCancer Researchen_US
dc.subject.otherOncologyen_US
dc.subject.otherHematologyen_US
dc.subject.otherSurgical Oncologyen_US
dc.subject.otherCancer Therapyen_US
dc.subject.otherLungen_US
dc.subject.otherMurineen_US
dc.subject.otherSpontaneous Metastasisen_US
dc.subject.otherSurgeryen_US
dc.subject.otherTumor Modelen_US
dc.titleA BALB/c murine lung alveolar carcinoma used to establish a surgical spontaneous metastasis modelen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelOncology and Hematologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDivision of Surgical Oncology, , University of Michigan, , , Ann Arbor, , Michigan, , USA,en_US
dc.contributor.affiliationotherDepartment of Microbiology and Immunology, , State University of New York at Buffalo, , , Buffalo, , New York, , USA, ; Department of Surgery, , State University of New York at Buffalo, , , Buffalo, , New York, , USA,en_US
dc.contributor.affiliationotherDepartment of Microbiology and Immunology, , State University of New York at Buffalo, , , Buffalo, , New York, , USA,en_US
dc.contributor.affiliationotherDepartment of Microbiology and Immunology, , State University of New York at Buffalo, , , Buffalo, , New York, , USA,en_US
dc.contributor.affiliationotherDepartment of Surgery, , State University of New York at Buffalo, , , Buffalo, , New York, , USA,en_US
dc.contributor.affiliationotherJ.G. Brown Cancer Center and the Department of Microbiology and Immunology, , University of Louisville, , , Louisville, , Kentucky, USA,en_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid15554393en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/42586/1/10585_2004_Article_DO00000954.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1023/B:CLIN.0000046176.33867.c5en_US
dc.identifier.sourceClinical & Experimental Metastasisen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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