Digital Archives Initiative
Memorial University - Electronic Theses and Dissertations 4
menu off  add document to favorites : add page to favorites : reference url back to results : previous : next
 
 Search this object:
  
 0 hit(s) :: previous hit : next hit
  View:    
  previous page : next page
Document Description
TitleInhibition of sanguinarine induced bimodal cell death by aurin tricarboxylic acid but not by cycloheximide
AuthorHallock, Sarathi C., 1968-
DescriptionThesis (M.Sc.)--Memorial University of Newfoundland, 2001. Medicine
Date2001
Paginationxii, 154 leaves : ill. (some col.)
SubjectCell death; Apoptosis; Leukemia--Immunological aspects;
Subject.MESHCell Death; Apoptosis; Leukemia--immunology;
DegreeM.Sc.
Degree GrantorMemorial University of Newfoundland. Faculty of Medicine.
DisciplineMedicine
LanguageEng
NotesBibliography: leaves 123-154
AbstractThe possible role of endonuclease and protein synthesis inhibition by aurin tricarboxylic acid (ATA) and by cycloheximide (CHX) respectively was investigated in sanguinarine induced apoptosis (PCD) and blister cell death (BCD) in K562 erythroleukemia cells. -- Studies in our laboratory have consistently shown that when K562 cells are treated with sanguinarine - a quaternary benzophenanthridine alkaloid which is reported to inhibit protein kinase C and nuclear factor NF-κB, at concentrations of 1.5 μg/ml for 2hrs induced the morphology of PCD, and at concentrations of 12.5 μg/ml for 2 hrs the morphology of BCD (blister formation). This phenomenon of dual cell death modality was termed "bimodal cell death" or BMCD (Liepins et al., 1996). -- The role of endonuclease activity and protein synthesis in PCD and BCD was assessed by the capacity of ATA and CHX respectively, to inhibit these processes. This was investigated by pretreating cells with ATA and CHX prior to sanguinarine treatment and subsequently measuring their effects on bimodal cell death using a host of standard methods: light microscopy and quantitative morphology; electron microscopy; terminal dUTP mediated nick end labelling (TUNEL) assay; annexin V binding assay (fluorescence microscopic and flow cytometric analysis); 51Cr release assay; DNA content analysis by flowcytometry; oxygen consumption studies; trypan blue assay. Results show that, while ATA pretreatment of cells inhibited PCD almost completely and BCD by 30-40%, CHX pretreatment failed to inhibit PCD and BCD. This may indicate the importance of endonuclease in sanguinarine induced PCD and to some extent in BCD. This may also signify the importance of post-translational modification of proteins rather than their de novo synthesis in both these forms of cell death. -- Discovering new drugs and understanding their mechanisms of action may lead to more effective administration of these agents with other more established therapeutics in the treatment of cancer. To this end, better understanding the mechanism of PCD and identifying novel forms of cell death like BCD, would contribute in no small measure.
TypeText
FormatImage/jpeg; Application/pdf
SourcePaper copy kept in the Centre for Newfoundland Studies, Memorial University Libraries
Local Identifiera1522797
RightsThe author retains copyright ownership and moral rights in this thesis. Neither the thesis nor substantial extracts from it may be printed or otherwise reproduced without the author's permission.
CollectionElectronic Theses and Dissertations
Scanning StatusCompleted
PDF File(15.77 MB) -- http://collections.mun.ca/PDFs/theses/Hallock_SarathiC.pdf
CONTENTdm file name140988.cpd