Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/122492
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dc.titleMOLECULAR MECHANISMS OF THE PROTO-ONCOGENE BCL6 IN GLIOBLASTOMA
dc.contributor.authorCHEN YE
dc.date.accessioned2016-02-12T18:00:16Z
dc.date.available2016-02-12T18:00:16Z
dc.date.issued2015-07-29
dc.identifier.citationCHEN YE (2015-07-29). MOLECULAR MECHANISMS OF THE PROTO-ONCOGENE BCL6 IN GLIOBLASTOMA. ScholarBank@NUS Repository.
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/122492
dc.description.abstractZBTB TRANSCRIPTION FACTORS ORCHESTRATE GENE EXPRESSION DURING HUMAN DEVELOPMENT. HOWEVER, THEIR ROLES IN GLIOBLASTOMA MULTIFORME (GBM) REMAIN LARGELY UNEXPLORED. HERE I IDENTIFY BCL6, AN ONCOGENIC PROTEIN IN LYMPHOMA, AS AN IMPORTANT GLIOMA-PROMOTING FACTOR. BCL6 EXPRESSION IS ELEVATED IN AND NECESSARY FOR THE GROWTH OF GBM. BCL6 MODULATES THE EXPRESSION OF TP53, AXL AND MET. THE ACTIVATED BCL6-AXL SIGNALS THROUGH MEK-ERK AND S6K-RPS6 AXES, AND PROMOTES CAP-DEPENDENT TRANSLATION. MOREOVER, DEPLETION OF BCL6 OR PHARMACOLOGICAL INHIBITION OF BCL6/NCOR COMPLEX EFFECTIVELY BLOCKS GBM GROWTH. TOGETHER, THESE FINDINGS UNCOVER A NOVEL GROWTH PROMOTING ROLE OF BCL6 IN GBM, AND PROVIDE THE RATIONALE AND EVIDENCE TO TARGET THIS PROTEIN IN GBM TREATMENT.
dc.language.isoen
dc.subjectBCL6, Glioblastoma, ZBTB, TP53, AXL
dc.typeThesis
dc.contributor.departmentCANCER SCIENCE INSTITUTE OF SINGAPORE
dc.contributor.supervisorH. PHILLIP KOEFFLER
dc.description.degreePh.D
dc.description.degreeconferredPHD IN CANCER BIOLOGY
dc.identifier.isiutNOT_IN_WOS
Appears in Collections:Ph.D Theses (Open)

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