Glioblastoma Multiforme (GBM) is the most common and aggressive primary malignant brain tumor in adults. With an average survival of only 12-16 months the prognosis for GBM patients remains dismal, with less than 5% of patients surviving 5 years. New mechanism-based approaches are necessary for the management of patients with GBM. Many GBM tumors are believed to be caused by self-renewing, glioblastoma-derived stem-like cells (GSCs). These GSCs are resistant to chemo- and radiation therapies, and are believed to be responsible for tumor recurrence. In a recent paper from our lab we have shown that REST, RE1-silencing transcription factor, regulates oncogenic properties such as proliferation, invasion, and apoptosis in GSCs. However, the mechanism by which REST regulates oncogenic properties of GSCs is not clearly understood. Thus, the overall aim of this project is to delineate the mechanism by which REST mediates oncogenic properties of GSCs. Using genome-wide expression analysis followed by biochemical validations, we show that REST targets two microRNAs, miR-124 and miR-203 in High REST GSCs (HR-GSCs). Independent studies were carried out to determine the role of these microRNAs in HR-GSC derived brain tumors. Gain of function of either miR-124 or miR-203 in HR-GSCs leads to increased survival when tumor cells are transplanted into mice. Importantly, the increased survival of tumor-bearing mice caused by knockdown of Rest in HR-GSCs can be reversed by double knockdown of Rest and miR-124 or miR-203, indicating that the REST-miR-124/miR-203 axis controls tumorigenesis. We further show that the REST-miR-124 axis regulates proliferation, invasion and apoptosis of GSCs both in vitro and in vivo, while the REST-miR-203 axis specifically regulates invasion and not proliferation or apoptosis. Our results indicate that invasion is a major hallmark of HR-GSC tumors and that the REST-miR-124/203 axis is critical in this process. These results also suggest that the REST-miR-124/203 axis could potentially be targeted in therapeutic approaches to block invasion in REST-stratified GBM tumors.
","abstract_html":"<p>Glioblastoma Multiforme (GBM) is the most common and aggressive primary malignant brain tumor in adults. With an average survival of only 12-16 months the prognosis for GBM patients remains dismal, with less than 5% of patients surviving 5 years. New mechanism-based approaches are necessary for the management of patients with GBM. Many GBM tumors are believed to be caused by self-renewing, glioblastoma-derived stem-like cells (GSCs). These GSCs are resistant to chemo- and radiation therapies, and are believed to be responsible for tumor recurrence. In a recent paper from our lab<em> </em>we have shown that REST, RE1-silencing transcription factor, regulates oncogenic properties such as proliferation, invasion, and apoptosis in GSCs. However, the mechanism by which REST regulates oncogenic properties of GSCs is not clearly understood. Thus, the overall aim of this project is to delineate the mechanism by which REST mediates oncogenic properties of GSCs. Using genome-wide expression analysis followed by biochemical validations, we show that REST targets two microRNAs, miR-124 and miR-203 in High REST GSCs (HR-GSCs). Independent studies were carried out to determine the role of these microRNAs in HR-GSC derived brain tumors. Gain of function of either miR-124 or miR-203 in HR-GSCs leads to increased survival when tumor cells are transplanted into mice. Importantly, the increased survival of tumor-bearing mice caused by knockdown of Rest in HR-GSCs can be reversed by double knockdown of Rest and miR-124 or miR-203, indicating that the REST-miR-124/miR-203 axis controls tumorigenesis. We further show that the REST-miR-124 axis regulates proliferation, invasion and apoptosis of GSCs both <em>in vitro</em> and <em>in vivo</em>, while the REST-miR-203 axis specifically regulates invasion and not proliferation or apoptosis. Our results indicate that invasion is a major hallmark of HR-GSC tumors and that the REST-miR-124/203 axis is critical in this process. These results also suggest that the REST-miR-124/203 axis could potentially be targeted in therapeutic approaches to block invasion in REST-stratified GBM tumors.</p>","abstract_has_math":false,"creators":["Marisetty, Anantha L"],"institution":null,"degree_name":"Doctor of Philosophy (PhD)","degree_level":"Dissertation (PhD)","degree_discipline":null,"degree_department":null,"school":null,"contributors":["Sadhan Majumder , PhD","Gary Gallick , PhD","Greg Fuller , M.D, PhD"],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2015,"date_issued":"2015-05-01T07:00:00Z","date_published":"2015-05-01T07:00:00Z","updated_at":"2026-07-24T05:49:30Z","subjects":["Glioblastoma","Glioblastoma Stem cells","MicroRNAs","Apoptosis","Invasion","Microarray","Biology","Medicine and Health Sciences"],"languages":[],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://digitalcommons.library.tmc.edu/utgsbs_dissertations/584","outbound_label":"Repository record","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Sadhan Majumder , PhD","Gary Gallick , PhD","Greg Fuller , M.D, PhD"]},{"key":"dc:creator","label":"Author","values":["Marisetty, Anantha L"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.available","label":"Dc Date Available","values":["2016-05-10T07:00:00Z"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Dissertation (PhD)"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Doctor of Philosophy (PhD)"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Glioblastoma","Glioblastoma Stem cells","MicroRNAs","Apoptosis","Invasion","Microarray","Biology","Medicine and Health Sciences"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["https://digitalcommons.library.tmc.edu/utgsbs_dissertations/584"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["Glioblastoma Multiforme (GBM) is the most common and aggressive primary malignant brain tumor in adults. With an average survival of only 12-16 months the prognosis for GBM patients remains dismal, with less than 5% of patients surviving 5 years. New mechanism-based approaches are necessary for the management of patients with GBM. Many GBM tumors are believed to be caused by self-renewing, glioblastoma-derived stem-like cells (GSCs). These GSCs are resistant to chemo- and radiation therapies, and are believed to be responsible for tumor recurrence. In a recent paper from our lab we have shown that REST, RE1-silencing transcription factor, regulates oncogenic properties such as proliferation, invasion, and apoptosis in GSCs. However, the mechanism by which REST regulates oncogenic properties of GSCs is not clearly understood. Thus, the overall aim of this project is to delineate the mechanism by which REST mediates oncogenic properties of GSCs. Using genome-wide expression analysis followed by biochemical validations, we show that REST targets two microRNAs, miR-124 and miR-203 in High REST GSCs (HR-GSCs). Independent studies were carried out to determine the role of these microRNAs in HR-GSC derived brain tumors. Gain of function of either miR-124 or miR-203 in HR-GSCs leads to increased survival when tumor cells are transplanted into mice. Importantly, the increased survival of tumor-bearing mice caused by knockdown of Rest in HR-GSCs can be reversed by double knockdown of Rest and miR-124 or miR-203, indicating that the REST-miR-124/miR-203 axis controls tumorigenesis. We further show that the REST-miR-124 axis regulates proliferation, invasion and apoptosis of GSCs both in vitro and in vivo, while the REST-miR-203 axis specifically regulates invasion and not proliferation or apoptosis. Our results indicate that invasion is a major hallmark of HR-GSC tumors and that the REST-miR-124/203 axis is critical in this process. These results also suggest that the REST-miR-124/203 axis could potentially be targeted in therapeutic approaches to block invasion in REST-stratified GBM tumors.
"]},{"key":"dc:title","label":"Title","values":["Rest Regulatory Circuit Controls Distinct Oncogenic Properties of Glioblastoma Stem Cells Through Specific Micrornas"]}]}],"canonical_facts":{"dc:contributor":["Sadhan Majumder , PhD","Gary Gallick , PhD","Greg Fuller , M.D, PhD"],"dc:creator":["Marisetty, Anantha L"],"dc:date.available":["2016-05-10T07:00:00Z"],"dc:description.abstract":["Glioblastoma Multiforme (GBM) is the most common and aggressive primary malignant brain tumor in adults. With an average survival of only 12-16 months the prognosis for GBM patients remains dismal, with less than 5% of patients surviving 5 years. New mechanism-based approaches are necessary for the management of patients with GBM. Many GBM tumors are believed to be caused by self-renewing, glioblastoma-derived stem-like cells (GSCs). These GSCs are resistant to chemo- and radiation therapies, and are believed to be responsible for tumor recurrence. In a recent paper from our lab we have shown that REST, RE1-silencing transcription factor, regulates oncogenic properties such as proliferation, invasion, and apoptosis in GSCs. However, the mechanism by which REST regulates oncogenic properties of GSCs is not clearly understood. Thus, the overall aim of this project is to delineate the mechanism by which REST mediates oncogenic properties of GSCs. Using genome-wide expression analysis followed by biochemical validations, we show that REST targets two microRNAs, miR-124 and miR-203 in High REST GSCs (HR-GSCs). Independent studies were carried out to determine the role of these microRNAs in HR-GSC derived brain tumors. Gain of function of either miR-124 or miR-203 in HR-GSCs leads to increased survival when tumor cells are transplanted into mice. Importantly, the increased survival of tumor-bearing mice caused by knockdown of Rest in HR-GSCs can be reversed by double knockdown of Rest and miR-124 or miR-203, indicating that the REST-miR-124/miR-203 axis controls tumorigenesis. We further show that the REST-miR-124 axis regulates proliferation, invasion and apoptosis of GSCs both in vitro and in vivo, while the REST-miR-203 axis specifically regulates invasion and not proliferation or apoptosis. Our results indicate that invasion is a major hallmark of HR-GSC tumors and that the REST-miR-124/203 axis is critical in this process. These results also suggest that the REST-miR-124/203 axis could potentially be targeted in therapeutic approaches to block invasion in REST-stratified GBM tumors.
"],"dc:identifier":["https://digitalcommons.library.tmc.edu/utgsbs_dissertations/584"],"dc:subject":["Glioblastoma","Glioblastoma Stem cells","MicroRNAs","Apoptosis","Invasion","Microarray","Biology","Medicine and Health Sciences"],"dc:title":["Rest Regulatory Circuit Controls Distinct Oncogenic Properties of Glioblastoma Stem Cells Through Specific Micrornas"],"thesis:degree_level":["Dissertation (PhD)"],"thesis:degree_name":["Doctor of Philosophy (PhD)"]},"updated_at":"2026-07-24T05:49:30Z"}