Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/61806
Title: Genomic profiling of medulloblastomas
Authors: Teo, Wan-Yee
Keywords: DRNTU::Science::Biological sciences
Issue Date: 2012
Source: Teo, W.-Y. (2012). Genomic profiling of medulloblastomas. Doctoral thesis, Nanyang Technological University, Singapore.
Abstract: Medulloblastoma is the most common malignant brain tumor in children. Multimodality treatment regimens involving surgery, chemotherapy and radiotherapy, have significantly improved survival rates for this disease; however, approximately one third of patients with medulloblastoma remain incurable and current treatment result in severe neurocognitive sequelae among long term survivors. Outcome prediction using clinical parameters and biomarkers has failed, owing to the biological heterogeneity of medulloblastomas. Molecular profiling offers an attractive approach for risk stratification of treatment and has identified at least two distinct subgroups of medulloblastoma with activation of sonic hedgehog and Wingless pathways; the remaining subgroups are poorly defined. Granule cell precursors are believed to be the cell of origin of at least a subset of medulloblastoma. Aim 1: We hypothesized that the gene expression of medulloblastoma is possibly accounted for by not only the pathogenesis of the tumor, but also the cell of origin. We hypothesized that the medulloblastoma subgroups which are non-sonic-hedgehog-activated arise from a different cell of origin and speculate that knowledge on the identity of the cell of origin may provide insights to the tumorigenesis of the poorly understood subgroups of tumors. We also explored independent prognostic biological markers within each molecularly distinct medulloblastoma subgroup for higher clinical utility. Aim 2: To elucidate the role of the immune system in the biology and clinical outcome of medulloblastoma, we hypothesize that immune cells infiltrating medulloblastoma create a unique microenvironment which may alter the tumor biology an immune-regulated gene expression signature that can be linked to prognostic outcome.
URI: http://hdl.handle.net/10356/61806
Fulltext Permission: restricted
Fulltext Availability: With Fulltext
Appears in Collections:SBS Theses

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