Involvement of Estrogen Receptor Beta 5 in the Progression of Glioma

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dc.contributor.advisorShaohua Yang
dc.creatorLi, Wenjun
dc.date.accessioned2019-08-22T19:33:31Z
dc.date.available2019-08-22T19:33:31Z
dc.date.issued2013-05-01
dc.date.submitted2013-04-29T14:36:05-07:00
dc.description.abstractEmerging evidence suggests a decline of ERβ expression in various peripheral cancers and ERβ has been proposed as a cancer brake that inhibits tumor cell growth and proliferation. In the current study, we have identified ERβ5 as the predominant isoform of ERβ in human glioma and its expression was significantly increased in human glioma as compared with non-neoplastic brain tissue. Hypoxia and activation of hypoxia inducible factor (HIF) increased ERβ transcription in U87 cells, suggesting elevated ERβ expression in glioma might be induced by the hypoxic stress in the tumor. Overexpression of either ERβ1 or ERβ5 increased PTEN expression and inhibited activation of the PI3K/AKT/mTOR pathway; ERβ5 also inhibited the MAPK/ERK pathway. In U87 cells, ERβ1 and ERβ5 decreased cell proliferation and decreased cells in the S+G2/M phase. Our findings suggest hypoxia induced ERβ5 expression in glioma as a self-protective mechanism against tumor proliferation and that ERβ5 might serve as a therapeutic target for the treatment of glioma. We also reported potential association between ERβ expression and outcomes of TMZ or tamoxifen treatment for GBM, which might be of practical clinical values.
dc.format.mimetypeapplication/pdf
dc.identifier.urihttps://hdl.handle.net/20.500.12503/26203
dc.language.isoen
dc.provenance.legacyDownloads379
dc.subjectCancer Biology
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.subjectOncology
dc.subjectEstrogen
dc.subjectGlioma
dc.subjectCancer
dc.subjecttmz
dc.subjectTamoxifen
dc.titleInvolvement of Estrogen Receptor Beta 5 in the Progression of Glioma
dc.typeDissertation
dc.type.materialtext
thesis.degree.departmentGraduate School of Biomedical Sciences
thesis.degree.disciplinePharmacology and Neuroscience
thesis.degree.grantorUniversity of North Texas Health Science Center at Fort Worth
thesis.degree.nameDoctor of Philosophy

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