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Multiple growth factor independence in rat mammary carcinoma cells

dc.contributor.authorMoorthy, Rameshen_US
dc.contributor.authorEthier, Stephen P.en_US
dc.date.accessioned2006-09-11T14:25:32Z
dc.date.available2006-09-11T14:25:32Z
dc.date.issued1991-05en_US
dc.identifier.citationEthier, Stephen P.; Moorthy, Ramesh; (1991). "Multiple growth factor independence in rat mammary carcinoma cells." Breast Cancer Research and Treatment 18(2): 73-81. <http://hdl.handle.net/2027.42/44197>en_US
dc.identifier.issn0167-6806en_US
dc.identifier.issn1573-7217en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/44197
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=1912610&dopt=citationen_US
dc.description.abstractIn previous studies we demonstrated that rat mammary tumor (RMT) cells that are serially transplantable consist of cells that are independent of growth factors strictly required by normal rat mammary epithelial (RME) cells for growth in serum-free culture. The present studies were designed to determine the extent of the growth factor independence of several cell lines derived from these tumors and to determine if the cells that expressed growth factor independence in vitro are also tumorigenic in vivo . Cells from a transplantable mammary carcinoma (8–12 RMT) were seeded into culture in serum-free medium in the absence of either insulin (IN), epidermal growth factor (EGF), or cholera toxin (CT), and cell populations independent of the individual factors were developed. Next, the three growth factor independent populations were tested for their ability to grow in the absence of multiple growth factors. 8–12 RMT cells did not lose proliferative potential when multiple growth factors were deleted from the medium. Indeed, 8–12 RMT cells could be serially propagated in serum-free medium supplemented solely with bovine serum albumin (BSA) and ethanolamine. Cell lines independent of single growth factors were also developed from two other transplantable tumors (1–9 RMT and 7–15 RMT). In contrast to the 8–12 RMT-derived cell lines, deletion of additional growth factors from the media of the 1–9 RMT and 7–15 RMT-derived cells resulted in dramatic losses in growth potential. These results suggest that independence of individual growth factors is mediated by different mechanisms, since cells from different tumors can stably express independence of one, two, or three or more factors. Examination of conditioned media of four different RMT cell lines indicates that independence of EGF is mediated by autocrine factors. By contrast, there is no evidence for an autocrine factor that mediates independence of insulin-like growth factors. Thus, cell lines derived from serially transplantable RMTs are independent of either single or multiple growth factors, and independence of individual growth factors appears to be mediated by separate mechanisms.en_US
dc.format.extent860249 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.otherOncologyen_US
dc.subject.otherGrowth Factor Independenceen_US
dc.subject.otherMedicine & Public Healthen_US
dc.subject.otherAutocrine Factorsen_US
dc.subject.otherCholera Toxinen_US
dc.subject.otherEpidermal Growth Factoren_US
dc.subject.otherInsulinen_US
dc.subject.otherRat Mammary Tumorsen_US
dc.titleMultiple growth factor independence in rat mammary carcinoma cellsen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbsecondlevelNeurosciencesen_US
dc.subject.hlbsecondlevelOncology and Hematologyen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbsecondlevelOphthalmologyen_US
dc.subject.hlbsecondlevelOtolaryngologyen_US
dc.subject.hlbsecondlevelObstetrics and Gynecologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Radiation Oncology, The University of Michigan Medical School, 1331 E. Ann St., 48109, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumDepartment of Radiation Oncology, The University of Michigan Medical School, 1331 E. Ann St., 48109, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid1912610en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/44197/1/10549_2005_Article_BF01980969.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF01980969en_US
dc.identifier.sourceBreast Cancer Research and Treatmenten_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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