Treatment for acute myeloid leukemia (AML) has changed little in the past four decades. For the majority of AML patients, current treatment options include chemotherapy and allogeneic stem cell transplants, which also involves high-dose chemotherapy or radiation treatment. These options have little success in the long-run, as only an estimated 26% of patients survive five years post-diagnosis. In efforts to address this low survival rate, interest has increased for targeting epigenetic pathways in AML. This focus stems from the discovery that AML is frequently driven by blockades on hematopoietic stem cell differentiation, which involves a series of coordinated epigenetic changes. Given its reported roles as an epigenetic reader, stem cell regulator, and known oncogene, we investigated TRIM24 for putative relevance in AML. Expression data from previous studies have also suggested roles for TRIM24 in chronic myeloid leukemia and acute lymphocytic leukemia; however, no studies to date have reported measurements of TRIM24 in AML from an in vivo system. Here, we report that low TRIM24 mRNA expression in human AML patients (in TCGA) correlates with poor survival. Additionally, this association was found to be independent of gene expression signatures of prognostic significance, such as Gentles leukemic stem cell signature. Furthermore, loss of Trim24 in murine, MLL-AF9-driven AML worsened survival and increased leukemic stem cell numbers, while having no observed effects on normal hematopoiesis. These results lay the groundwork for future investigations of the role of TRIM24 in AML, which has the potential to aid development of novel therapeutic strategies.
","abstract_html":"<p>Treatment for acute myeloid leukemia (AML) has changed little in the past four decades. For the majority of AML patients, current treatment options include chemotherapy and allogeneic stem cell transplants, which also involves high-dose chemotherapy or radiation treatment. These options have little success in the long-run, as only an estimated 26% of patients survive five years post-diagnosis. In efforts to address this low survival rate, interest has increased for targeting epigenetic pathways in AML. This focus stems from the discovery that AML is frequently driven by blockades on hematopoietic stem cell differentiation, which involves a series of coordinated epigenetic changes. Given its reported roles as an epigenetic reader, stem cell regulator, and known oncogene, we investigated <em>TRIM24</em> for putative relevance in AML. Expression data from previous studies have also suggested roles for <em>TRIM24</em> in chronic myeloid leukemia and acute lymphocytic leukemia; however, no studies to date have reported measurements of <em>TRIM24</em> in AML from an <em>in</em> <em>vivo</em> system. Here, we report that low <em>TRIM24</em> mRNA expression in human AML patients (in TCGA) correlates with poor survival. Additionally, this association was found to be independent of gene expression signatures of prognostic significance, such as Gentles leukemic stem cell signature. Furthermore, loss of <em>Trim24</em> in murine, <em>MLL</em>-<em>AF9</em>-driven AML worsened survival and increased leukemic stem cell numbers, while having no observed effects on normal hematopoiesis. These results lay the groundwork for future investigations of the role of <em>TRIM24</em> in AML, which has the potential to aid development of novel therapeutic strategies.</p>","abstract_has_math":false,"creators":["Shaw, Justin","https://orcid.org/0000-0001-7166-1322
"],"institution":null,"degree_name":"Masters of Science (MS)","degree_level":"Thesis (MS)","degree_discipline":null,"degree_department":null,"school":null,"contributors":["Margarida Santos","Michelle Barton","Xiaobing Shi"],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2018,"date_issued":"2018-05-01T07:00:00Z","date_published":"2018-05-01T07:00:00Z","updated_at":"2026-07-24T05:48:59Z","subjects":["Leukemia","AML","Hematopoiesis","Hematopoietic","Stem cell","MLL","MLL-fusion","MLL-AF9","Cancer Biology","Molecular Genetics"],"languages":[],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://digitalcommons.library.tmc.edu/utgsbs_dissertations/833","outbound_label":"Repository record","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Margarida Santos","Michelle Barton","Xiaobing Shi"]},{"key":"dc:creator","label":"Author","values":["Shaw, Justin","https://orcid.org/0000-0001-7166-1322
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"]},{"key":"dc:title","label":"Title","values":["Trim24 In Normal & Malignant Hematopoiesis"]}]}],"canonical_facts":{"dc:contributor":["Margarida Santos","Michelle Barton","Xiaobing Shi"],"dc:creator":["Shaw, Justin","https://orcid.org/0000-0001-7166-1322
"],"dc:date.available":["2019-04-12T07:00:00Z"],"dc:description.abstract":["Treatment for acute myeloid leukemia (AML) has changed little in the past four decades. For the majority of AML patients, current treatment options include chemotherapy and allogeneic stem cell transplants, which also involves high-dose chemotherapy or radiation treatment. These options have little success in the long-run, as only an estimated 26% of patients survive five years post-diagnosis. In efforts to address this low survival rate, interest has increased for targeting epigenetic pathways in AML. This focus stems from the discovery that AML is frequently driven by blockades on hematopoietic stem cell differentiation, which involves a series of coordinated epigenetic changes. Given its reported roles as an epigenetic reader, stem cell regulator, and known oncogene, we investigated TRIM24 for putative relevance in AML. Expression data from previous studies have also suggested roles for TRIM24 in chronic myeloid leukemia and acute lymphocytic leukemia; however, no studies to date have reported measurements of TRIM24 in AML from an in vivo system. Here, we report that low TRIM24 mRNA expression in human AML patients (in TCGA) correlates with poor survival. Additionally, this association was found to be independent of gene expression signatures of prognostic significance, such as Gentles leukemic stem cell signature. Furthermore, loss of Trim24 in murine, MLL-AF9-driven AML worsened survival and increased leukemic stem cell numbers, while having no observed effects on normal hematopoiesis. These results lay the groundwork for future investigations of the role of TRIM24 in AML, which has the potential to aid development of novel therapeutic strategies.
"],"dc:identifier":["https://digitalcommons.library.tmc.edu/utgsbs_dissertations/833"],"dc:subject":["Leukemia","AML","Hematopoiesis","Hematopoietic","Stem cell","MLL","MLL-fusion","MLL-AF9","Cancer Biology","Molecular Genetics"],"dc:title":["Trim24 In Normal & Malignant Hematopoiesis"],"thesis:degree_level":["Thesis (MS)"],"thesis:degree_name":["Masters of Science (MS)"]},"updated_at":"2026-07-24T05:48:59Z"}