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dc.contributor.authorGross, Howarden_US
dc.date.accessioned2019-12-16T15:51:39Z
dc.date.available2019-12-16T15:51:39Z
dc.date.issued1999
dc.date.submitted1999
dc.identifier.other(OCoLC)44874337
dc.identifier.otherb2283977x
dc.identifier.urihttps://hdl.handle.net/2144/38896
dc.descriptionPLEASE NOTE: This work is protected by copyright. Downloading is restricted to the BU community: please click Download and log in with a valid BU account to access. If you are the author of this work and would like to make it publicly available, please contact open-help@bu.edu.en_US
dc.descriptionThesis (M.Sc.D.)--Boston University, Henry M. Goldman School of Dental Medicine, 1999 (Periodontology and Oral Biology).en_US
dc.descriptionIncludes bibliographical references (leaves 25-28).en_US
dc.description.abstractSuramin is an anticancer drug that normalizes the phenotype of some transformed cells. Preliminary studies show that suramin increases lysyl oxidase mRNA levels and causes phenotypic reversion of c-H-ras transformed NIH3T3 cells (RS485 cell line). Lysyl oxidase is an extracellular enzyme that catalyzes the final step for cross-linking and insolubilization of collagen and elastin in the extracellular matrix. It has been shown to act as a tumor suppressor. The purpose of this study was to determine whether the increase in lysyl oxidase mRNA levels is key to suramin’s effect on the phenotype of RS485 cells. This was accomplished by transfection of RS485 with an antisense lysyl oxidase expression vector and with empty vector (PCDNA3) followed by Southern blot and Northern blot analyses after suramin treatment of cells. Results show that two antisense clones (As 8, As 14) remain refractile in the presence of suramin while lysyl oxidase mRNA levels remain low, and control as pc16 and RS485 change morphology from refractile to flat while lysyl oxidase mRNA were increased. These results and other preliminary studies showing that suramin inhibits lysyl oxidase enzyme activity, suggest that lysyl oxidase mRNA in some way maintains normal cell phenotype. Further research should be done on cell kinetics, growth rate and morphology of these clones, grown in the presence and absence of suramin.en_US
dc.language.isoen_US
dc.publisherBoston Universityen_US
dc.rightsThis work is protected by copyright. Downloading is restricted to the BU community. If you are the author of this work and would like to make it publicly available, please contact open-help@bu.edu.en_US
dc.subjectCellen_US
dc.subjectProtein-lysine 6-oxidase.en_US
dc.subjectRna, messengeren_US
dc.subjectSuraminen_US
dc.titleThe relationship between cell morphology, suramin and lysyl oxidase mRNAen_US
dc.typeThesis/Dissertationen_US
etd.degree.nameMaster of Science in Denistryen_US
etd.degree.levelmastersen_US
etd.degree.disciplinePeriodontology and Oral Biologyen_US
etd.degree.grantorBoston Universityen_US


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