Receptor Cross-Talk in the Biology & Therapeutics Of Pediatric Rhabdoid Brain Tumors

atmire.migration.oldid2093
dc.contributor.advisorNarendran, Aru
dc.contributor.authorObaid, Halah
dc.date.accessioned2014-05-02T17:25:50Z
dc.date.available2014-06-16T07:00:39Z
dc.date.issued2014-05-02
dc.date.submitted2014en
dc.description.abstractAtypical teratoid rhabdoid tumor (ATRT) is a highly malignant brain tumor that usually affects very young children and typically causes death, despite very aggressive treatment. The biological properties contributing to tumor aggressiveness and resistance to common chemotherapeutic agents are currently unknown. Previous studies have shown the activation of Insulin like growth factor-I receptor (IGF-1R) in ATRT tumor specimens and cell lines. Additionally, angiogenesis is an established physiological mechanism that supports the survival and progression of brain tumors. Vascular endothelial growth factor receptor (VEGFR) signaling pathway is a major regulator of angiogenesis in brain tumors. We hypothesized that molecular interactions may exist between these two signaling pathways. Our findings show evidence for a novel IGF-1R/VEGFR-2 cross-talk in response to IGF-I mediated activation. Furthermore, we show evidence that the inhibition of IGF-1R/VEGFR-2 pathways by the small molecule inhibitors lead inhibition of cell migration properties and the initiation of apoptosis. Overall, the data generated in this set of studies present a framework to evaluate and utilize the receptor cross talk pathways to identify novel treatment approaches for ATRT in the future.en_US
dc.identifier.citationObaid, H. (2014). Receptor Cross-Talk in the Biology & Therapeutics Of Pediatric Rhabdoid Brain Tumors (Master's thesis, University of Calgary, Calgary, Canada). Retrieved from https://prism.ucalgary.ca. doi:10.11575/PRISM/27554en_US
dc.identifier.doihttp://dx.doi.org/10.11575/PRISM/27554
dc.identifier.urihttp://hdl.handle.net/11023/1481
dc.language.isoeng
dc.publisher.facultyGraduate Studies
dc.publisher.institutionUniversity of Calgaryen
dc.publisher.placeCalgaryen
dc.rightsUniversity of Calgary graduate students retain copyright ownership and moral rights for their thesis. You may use this material in any way that is permitted by the Copyright Act or through licensing that has been assigned to the document. For uses that are not allowable under copyright legislation or licensing, you are required to seek permission.
dc.subjectOncology
dc.subject.classificationReceptor Cross-Talken_US
dc.subject.classificationAtypical Teratoid Rhabdoid Tumoren_US
dc.titleReceptor Cross-Talk in the Biology & Therapeutics Of Pediatric Rhabdoid Brain Tumors
dc.typemaster thesis
thesis.degree.disciplineMedical Science
thesis.degree.grantorUniversity of Calgary
thesis.degree.nameMaster of Science (MSc)
ucalgary.item.requestcopytrue
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