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dc.contributorDepartment of Health Technology and Informaticsen_US
dc.creatorChan, Kam Hung Beny-
dc.identifier.urihttps://theses.lib.polyu.edu.hk/handle/200/7060-
dc.languageEnglishen_US
dc.publisherHong Kong Polytechnic University-
dc.rightsAll rights reserveden_US
dc.titleEffect of CAL-101 on gene regulation of phosphoinositol 3-kinase isoform p110δ in the pathogenesis of glioblastoma multiformeen_US
dcterms.abstractGlioblastoma multiforme (GBM) is the most highly invasive malignant brain tumor in humans. It is classified as Grade IV astrocytoma in accordance with the World Health Organization (WHO). Since GBM tumors are characterized by highly invasive and diffuse growth, surgical control of the disease is impossible. The standard treatment of GBM is ineffective with recurrent GBM due to the migration and insidious invasion abilities of glioma cells. In recent research, PI3K/ Akt signaling pathway is believed to mediate the proliferation, apoptosis, migration and invasion of glioma cells. Knockdown of p110δ reduces the migration and invasion ability of glioma cells in GBM. U87 human malignant glioblastoma cell line is used for analysis in this study in order to identify genes involved in migration and invasion of glioma cells. This cell line expresses all class IA PI3K isoforms and is well-characterized with PTEN-deficient status. U87MG cells were treated with different concentrations of CAL-101 with DMSO as carrier control. Total protein was analyzed for p110δ, phospho-Akt (Ser⁴⁷³), phospho-Akt (Thr³⁰⁸), total Akt and β-actin, in order to identify the optimal concentration of CAL-101 with reduced protein expression of phospho-Akt. Gene expression in treated cells and carrier control cells were analyzed with extracellular matrix and adhesion molecules 96 well plates by PCR array using the Real-Time 7500 PCR system. Relative quantification of individual gene was analyzed by DataAssist software. Level of gene expression was expressed with fold change ((2^(-ΔΔCt)) according to the cycle threshold (Ct) values of the genes. It was revealed that gene for ADAMTS1 was up-regulated with fold change of 2.7, while COL11A1 gene was down-regulated with fold change of 3.0 after treatment with 5 μM CAL-101 for 24 hours. Genes of downstream pathways could be significantly affected by the activity of p110δ. Isoform-specific inhibitor may be a better way to treat glioma patients, for efficient control of glioma cell migration and invasion.en_US
dcterms.extentxii, 79 leaves : ill. (some col.) ; 30 cm.en_US
dcterms.isPartOfPolyU Electronic Thesesen_US
dcterms.issued2013en_US
dcterms.educationalLevelAll Masteren_US
dcterms.educationalLevelM.Sc.en_US
dcterms.LCSHPhosphoinositides.en_US
dcterms.LCSHGliomas -- Treatment.en_US
dcterms.LCSHGlioblastoma multiformeen_US
dcterms.LCSHHong Kong Polytechnic University -- Dissertationsen_US
dcterms.accessRightsrestricted accessen_US

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Please use this identifier to cite or link to this item: https://theses.lib.polyu.edu.hk/handle/200/7060