Characterization of Gene Expression During Adenosine 3':5'-Cyclic Monophosphate Induced Neuroendocrine Differentiation in Human Prostatic Adenocarcinoma

dc.contributor.authorGoodin, Jeremy Leeen
dc.contributor.committeechairRutherford, Charles L.en
dc.contributor.committeememberStevens, Ann M.en
dc.contributor.committeememberDenbow, Cynthia J.en
dc.contributor.committeememberWong, Eric A.en
dc.contributor.committeememberSible, Jill C.en
dc.contributor.departmentBiologyen
dc.date.accessioned2014-03-14T20:09:26Zen
dc.date.adate2002-04-19en
dc.date.available2014-03-14T20:09:26Zen
dc.date.issued2002-04-03en
dc.date.rdate2003-04-19en
dc.date.sdate2002-04-12en
dc.description.abstractThe LNCaP cell line is a versatile and useful model that is suitable for the study of human prostate cancer in vitro. The elevation of LNCaP intracellular cAMP levels through the addition of membrane permeable cAMP analogues, phosphodiesterase inhibitors, adenylate cyclase activators, or components of the cAMP signal transduction pathway can induce reversible neuroendocrine differentiation. Elucidation of those genes that are differentially expressed between undifferentiated prostate cancer cells and prostate cancer cells that have been induced to differentiate may present new insights for the molecular mechanisms governing neuroendocrine differentiation, early detection of prostate cancer, and/or potential targets for gene therapy. In this study, differential display PCR was used to identify 226 differentially expressed PCR products. Twelve of the differential display PCR products were confirmed by Northern blot analysis and cloned. DNA sequencing and database comparisons were performed. Among the differentially expressed genes, the human ribosomal S3a gene was identified as down regulated in response to LNCaP differentiation. In order to better ascertain the mechanism by which HRS3a gene expression is decreased during differentiation, the promoter region for this gene was analyzed. Electrophoretic mobility shift assay, antibody supershift assays, site-directed mutagenesis, and luciferase reporter gene analysis were employed to authenticate the roles of several transcription factors in the regulation of the HRS3a gene. Two cyclic AMP response elements, a Sp1 element and a GA-binding protein element, were involved in the regulation of HRS3a gene expression. In order to ascertain the effect of HRS3a down regulation in LNCaP cells, antisense phosphorothioate oligonucleotides were designed to inhibit HRS3a gene expression. Treatment of LNCaP cells with antisense HRS3a oligonucleotides did not influence cAMP induced neuroendocrine differentiation but antisense treatment did result in a decrease in LNCaP cell growth. In addition, it was determined that morphological changes associated with cAMP induced differentiation of LNCaP cells from the epithelial to the neuroendocrine state may not require alterations in gene expression nor the expression of novel proteins.en
dc.description.degreePh. D.en
dc.identifier.otheretd-04122002-005459en
dc.identifier.sourceurlhttp://scholar.lib.vt.edu/theses/available/etd-04122002-005459/en
dc.identifier.urihttp://hdl.handle.net/10919/26791en
dc.publisherVirginia Techen
dc.relation.haspartjergood3.pdfen
dc.rightsIn Copyrighten
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/en
dc.subjectdifferentiationen
dc.subjectprostate canceren
dc.subjectLNCaPen
dc.subjectcAMPen
dc.subjectneuroendocrineen
dc.titleCharacterization of Gene Expression During Adenosine 3':5'-Cyclic Monophosphate Induced Neuroendocrine Differentiation in Human Prostatic Adenocarcinomaen
dc.typeDissertationen
thesis.degree.disciplineBiologyen
thesis.degree.grantorVirginia Polytechnic Institute and State Universityen
thesis.degree.leveldoctoralen
thesis.degree.namePh. D.en
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