Search Results - "MacBeth, Kyle J"
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TP53 mutations in myelodysplastic syndromes and secondary AML confer an immunosuppressive phenotype
Published in Blood (10-12-2020)“…Somatic gene mutations are key determinants of outcome in patients with myelodysplastic syndromes (MDS) and secondary AML (sAML). In particular, patients with…”
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A comparison of azacitidine and decitabine activities in acute myeloid leukemia cell lines
Published in PloS one (02-02-2010)“…The cytidine nucleoside analogs azacitidine (AZA) and decitabine (DAC) are used for the treatment of patients with myelodysplastic syndromes and acute myeloid…”
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Leukemia stemness and co-occurring mutations drive resistance to IDH inhibitors in acute myeloid leukemia
Published in Nature communications (10-05-2021)“…Allosteric inhibitors of mutant IDH1 or IDH2 induce terminal differentiation of the mutant leukemic blasts and provide durable clinical responses in…”
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Phase I Study of Oral Azacitidine in Myelodysplastic Syndromes, Chronic Myelomonocytic Leukemia, and Acute Myeloid Leukemia
Published in Journal of clinical oncology (20-06-2011)“…To determine the maximum-tolerated dose (MTD), safety, pharmacokinetic and pharmacodynamic profiles, and clinical activity of an oral formulation of…”
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Pharmacokinetics and Pharmacodynamics with Extended Dosing of CC-486 in Patients with Hematologic Malignancies
Published in PloS one (21-08-2015)“…CC-486 (oral azacitidine) is an epigenetic modifier in development for patients with myelodysplastic syndromes and acute myeloid leukemia. In part 1 of this…”
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p53 protein expression independently predicts outcome in patients with lower-risk myelodysplastic syndromes with del(5q)
Published in Haematologica (Roma) (01-06-2014)“…Del(5q) myelodysplastic syndromes defined by the International Prognostic Scoring System as low- or intermediate-1-risk (lower-risk) are considered to have an…”
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The JAMM motif of human deubiquitinase Poh1 is essential for cell viability
Published in Molecular cancer therapeutics (01-01-2007)“…Poh1 deubiquitinase activity is required for proteolytic processing of polyubiquitinated substrates by the 26S proteasome, linking deubiquitination to complete…”
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Lenalidomide induces ubiquitination and degradation of CK1α in del(5q) MDS
Published in Nature (London) (09-07-2015)“…Lenalidomide is a highly effective treatment for myelodysplastic syndrome (MDS) with deletion of chromosome 5q (del(5q)). Here, we demonstrate that…”
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Molecular remission and response patterns in patients with mutant-IDH2 acute myeloid leukemia treated with enasidenib
Published in Blood (14-02-2019)“…Approximately 8% to 19% of patients with acute myeloid leukemia (AML) have isocitrate dehydrogenase-2 (IDH2) mutations, which occur at active site arginine…”
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Enasidenib, an inhibitor of mutant IDH2 proteins, induces durable remissions in older patients with newly diagnosed acute myeloid leukemia
Published in Leukemia (01-11-2019)“…Older adults with acute myeloid leukemia (AML) who are not fit for standard chemotherapy historically have poor outcomes. Approximately 12–15% of older…”
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Randomized Phase III Study of Lenalidomide Versus Placebo in RBC Transfusion-Dependent Patients With Lower-Risk Non-del(5q) Myelodysplastic Syndromes and Ineligible for or Refractory to Erythropoiesis-Stimulating Agents
Published in Journal of clinical oncology (01-09-2016)“…This international phase III, randomized, placebo-controlled, double-blind study assessed the efficacy and safety of lenalidomide in RBC transfusion-dependent…”
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Cytogenetics and gene mutations influence survival in older patients with acute myeloid leukemia treated with azacitidine or conventional care
Published in Leukemia (01-12-2018)“…Older patients with newly diagnosed acute myeloid leukemia (AML) in the phase 3 AZA-AML-001 study were evaluated at entry for cytogenetic abnormalities, and a…”
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Multiomics of azacitidine-treated AML cells reveals variable and convergent targets that remodel the cell-surface proteome
Published in Proceedings of the National Academy of Sciences - PNAS (08-01-2019)“…Myelodysplastic syndromes (MDS) and acute myeloid leukemia (AML) are diseases of abnormal hematopoietic differentiation with aberrant epigenetic alterations…”
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Randomised phase 2 study of pembrolizumab plus CC-486 versus pembrolizumab plus placebo in patients with previously treated advanced non-small cell lung cancer
Published in European journal of cancer (1990) (01-02-2019)“…Preclinical and early clinical studies suggest that combining epigenetic agents with checkpoint inhibitors can potentially improve outcomes in patients with…”
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Isoform Switching as a Mechanism of Acquired Resistance to Mutant Isocitrate Dehydrogenase Inhibition
Published in Cancer discovery (01-12-2018)“…Somatic mutations in cytosolic or mitochondrial isoforms of isocitrate dehydrogenase ( or , respectively) contribute to oncogenesis via production of the…”
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Enasidenib-induced differentiation promotes sensitivity to venetoclax in IDH2-mutated acute myeloid leukemia
Published in Leukemia (01-03-2022)Get full text
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Combination of azacitidine and enasidenib enhances leukemic cell differentiation and cooperatively hypomethylates DNA
Published in Experimental hematology (01-06-2021)“…•Enasidenib is an inhibitor of mutant IDH2 that releases the block in cellular differentiation imposed by aberrant production of 2-hydroxyglutarate.•Mechanisms…”
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Impact of somatic mutations on response to lenalidomide in lower-risk non-del(5q) myelodysplastic syndromes patients
Published in Leukemia (01-03-2021)Get full text
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Enasidenib in patients with mutant IDH2 myelodysplastic syndromes: a phase 1 subgroup analysis of the multicentre, AG221-C-001 trial
Published in The Lancet. Haematology (01-04-2020)“…Mutations in isocitrate dehydrogenase-2 (IDH2) occur in around 5% of patients with myelodysplastic syndromes. Neomorphic activity of mutant IDH2 proteins…”
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Lenalidomide as a disease-modifying agent in patients with del(5q) myelodysplastic syndromes: linking mechanism of action to clinical outcomes
Published in Annals of hematology (01-01-2014)“…Deletion of the long arm of chromosome 5, del(5q), is the most prevalent cytogenetic abnormality in patients with myelodysplastic syndromes (MDS). In…”
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