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dc.contributor.advisorLubahn, Dennis B. (Dennis Bryant), 1954-eng
dc.contributor.authorLu, Yuaneng
dc.date.issued2014eng
dc.date.submitted2014 Falleng
dc.description.abstractOrphan nuclear receptor Estrogen Receptor Related Receptor Beta (Esrrb) is a transcription factor. Although it was also shown to be important in cancer, little is known about its function in cancer cells and cancer relevant pathways. Using advanced molecular biology, bioinformatics, as well as system biology approaches, we found Esrrb-targeted genes in metastatic prostate cancer cells and distinguish a group of target genes responsive to the Esrrb selective ligand DY131. We also found Esrrb is strong regulator of oncogenic pathways Hedgehog signaling, Akt signaling and p53 signaling. Gene set enrichment analysis shows Esrrb are related to cell proliferation, regulation of apoptosis and transcription regulation, supporting its role as a transcription factor and its known function in inhibiting prostate cancer cells proliferation. Overall, our comprehensive analysis of Esrrb target genes and functions show that Esrrb is a significant factor regulating cellular proliferation and apoptosis. Its activity in regulating Hh-signaling target gene expression and Akt inhibitory effect indicates Esrrb can potentially serve as a therapeutic target in cancer treatment.eng
dc.identifier.urihttps://hdl.handle.net/10355/48215
dc.identifier.urihttps://doi.org/10.32469/10355/48215eng
dc.languageEnglisheng
dc.publisherUniversity of Missouri--Columbiaeng
dc.relation.ispartofcommunityUniversity of Missouri--Columbia. Graduate School. Theses and Dissertationseng
dc.rightsOpenAccess.eng
dc.rights.licenseThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 License.
dc.sourceSubmitted by the University of Missouri--Columbia Graduate Schooleng
dc.subject.FASTEstrogen -- Receptors -- Analysiseng
dc.subject.FASTProstate -- Cancer -- Treatmenteng
dc.subject.FASTNucleotide sequenceeng
dc.titleCharacterization of Esrrb function in metastatic prostate cancer cells and transcriptional regulation of hedgehog-signaling pathway target geneseng
dc.typeThesiseng
thesis.degree.disciplineBiochemistry (MU)eng
thesis.degree.grantorUniversity of Missouri--Columbiaeng
thesis.degree.levelDoctoraleng
thesis.degree.namePh. D.eng


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