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In vitro response of cervical cancer cell lines CaSki, HeLa, and ME-180 to the antiestrogen tamoxifen

dc.contributor.authorGrenman, Seija E.en_US
dc.contributor.authorShapira, Amnonen_US
dc.contributor.authorCarey, Thomas E.en_US
dc.date.accessioned2006-04-07T20:17:59Z
dc.date.available2006-04-07T20:17:59Z
dc.date.issued1988-06en_US
dc.identifier.citationGrenman, Seija, Shapira, Amnon, Carey, Thomas E. (1988/06)."In vitro response of cervical cancer cell lines CaSki, HeLa, and ME-180 to the antiestrogen tamoxifen." Gynecologic Oncology 30(2): 228-238. <http://hdl.handle.net/2027.42/27273>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6WG6-4C5H0T4-1CK/2/7695951b5ca44048c04defd17a93f952en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/27273
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=3371749&dopt=citationen_US
dc.description.abstractThe effect of tamoxifen, a nonsteroidal antiestrogenic drug, on the in vitro growth of three cell lines derived from carcinoma of the uterine cervix (HeLa, CaSki, ME-180) was studied using the breast cancer cell line MCF-7 as a tamoxifen-sensitive control. Logarithmically growing cells were fed daily with medium containing 5% dextran-charcoaltreated fetal bovine serum (D5) and 0, 1, 2.5, 5, 7.5, or 10 [mu]M tamoxifen. The cell number in replicate cultures was assessed every other day by cell counts. Growth inhibition was expressed as the percentage of the cell number in control cultures fed with D5. At a concentration of 5 [mu]M tamoxifen, a clear decrease in cell proliferation, resulting in 66-74% inhibition of growth, was observed with MCF-7, HeLa, and ME-180 after 6 days of exposure to tamoxifen. Doses greater than 5 [mu]M resulted in cytotoxicity and progressive cell loss. With the CaSki cell line, 2.5 [mu]M tamoxifen induced more than 60% growth inhibition and 5 [mu]M tamoxifen was cytotoxic. Tamoxifen-induced growth inhibition was reversed by removing tamoxifen from the cell cultures, and the cells resumed logarithmic growth after a lag period of 24-48 hr. MCF-7, but not the cervical carcinoma, lines required estradiol for complete and rapid recovery of logarithmic growth. Our results indicate that tamoxifen inhibits cell growth of these cervical carcinoma cell lines by a mechanism different from that in MCF-7.en_US
dc.format.extent783516 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleIn vitro response of cervical cancer cell lines CaSki, HeLa, and ME-180 to the antiestrogen tamoxifenen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbsecondlevelOtolaryngologyen_US
dc.subject.hlbsecondlevelOphthalmologyen_US
dc.subject.hlbsecondlevelOncology and Hematologyen_US
dc.subject.hlbsecondlevelObstetrics and Gynecologyen_US
dc.subject.hlbsecondlevelNeurosciencesen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumCancer Research Laboratory of the Department of Otolaryngology/Head and Neck Surgery, University of Michigan, Ann Arbor, Michigan 48109, U.S.A.; visiting fellow from the Department of Obstetrics and Gynecology, The University of Turku, Turku, Finlanden_US
dc.contributor.affiliationumCancer Research Laboratory of the Department of Otolaryngology/Head and Neck Surgery, University of Michigan, Ann Arbor, Michigan 48109, U.S.A.; Department of Otolarynology, Kaplan Hospital, Rehovot, Israelen_US
dc.contributor.affiliationumCancer Research Laboratory of the Department of Otolaryngology/Head and Neck Surgery, University of Michigan, Ann Arbor, Michigan 48109, U.S.A.en_US
dc.identifier.pmid3371749en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/27273/1/0000289.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0090-8258(88)90029-7en_US
dc.identifier.sourceGynecologic Oncologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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