| Vol. 12.30 – 3 August, 2021 |
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| Researchers showed that lysosomes were regulated dichotomously by transcription factor EB (TFEB) and MYC to balance catabolic and anabolic processes required for activating long-term-HSCs and guiding their lineage fate. [Cell Stem Cell] |
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| PUBLICATIONSRanked by the impact factor of the journal |
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| Scientists constructed a spatiotemporal transcriptome map of mouse fetal liver as a platform for experimental validation of novel regulatory mechanisms underlying HSC and multipotent progenitor expansion. [Cell Research] |
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| The authors used long-term quantitative single-cell imaging to show that lysosomes and active mitochondria were asymmetrically inherited in human blood stem cells and that their inheritance was a coordinated, non-random process. [Blood] |
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| In vitro treatment of Idh2R140Q/NHD13 thymocytes with enasidenib, a selective inhibitor of mutant IDH2, led to a marked decrease in leukemic cell proliferation, demonstrating that Idh2R140Q/NHD13 mice could serve as a useful in vivo model for the study of early/immature T cell precursor acute lymphoid leukemia (ALL) development and therapy. [Cancer Research] |
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| Researchers found that the RNA-binding protein IGF2BP3, which was overexpressed in mixed-lineage leukemia (MLL)-translocated leukemia, strongly amplified MLL-Af4-mediated leukemogenesis. [Leukemia] |
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| Investigators reported that TLR4 was expressed on granulo-monocytic progenitors, as well as mobilized human peripheral blood CD34+ cells. LPS, a component of Gram-negative bacteria that results in a systemic bacterial infection, induced the differentiation of peripheral blood CD34+ cells into myelocytes and monocytes in vitro via the TLR4 signaling pathway. [Journal of Immunology] |
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| Scientists showed that endogenous stimuli and VEGF were sufficient to induce robust human pluripotent stem cell-derived hematopoiesis, intensive generation of hematopoietic progenitors, maturation of blood cells and the emergence of definitive precursor cells including those that were phenotypically identical to early human embryonic HSCs. [Journal of Cellular and Molecular Medicine] |
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| The authors investigated the effect of ZEN-3365, a novel BRD4 inhibitor, on acute myeloid leukemia cells in regard to the Hedgehog pathway. [Annals of Hematology] |
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| In this single-center, Phase I trial, researchers administered anti-CD7 CAR T cells, manufactured from either previous stem cell transplantation donors or new donors to patients with relapsed or refractory T cell acute lymphoblastic leukemia [Journal of Clinical Oncology] |
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| Investigators analyzed 4708 adult acute myeloid leukemia patients recruited into Study Alliance Leukemia trials to investigate the prognostic impact of CEBPAsm. [Blood] |
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| Bisthianostat dose dependently induced acetylation of tubulin and H3 and increased PARP cleavage and apoptosis in RPMI-8226 cells. In RPMI-8226 and MM.1S cell xenograft mouse models, oral administration of bisthianostat for 18 days dose dependently inhibited tumor growth. [Acta Pharmacologica Sinica] |
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| The authors describe the wide-ranging role of AML1/ETO in acute myeloid leukemia (AML) leukemogenesis, with a particular focus on the aberrant epigenetic regulation of gene transcription driven by this AML-defining mutation. [Oncogene] |
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| Kronos Bio, Inc. announced the US FDA has cleared its Investigational New Drug Application for LANRA, allowing the company to proceed with a Phase I/II clinical trial of LANRA in patients with relapsed or refractory FLT3-mutated AML in combination with gilteritinib. [Kronos Bio, Inc.] |
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| February 17 – 20, 2022 Austin, Texas, United States |
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| University of Gothenburg – Gothenburg, Sweden |
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| Dalhousie University – Halifax, Nova Scotia, Canada |
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| Aarhus University – Aarhus, Denmark |
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| University of Wisconsin-Madison – Madison, Wisconsin, United States |
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| Heinrich Heine University Düsseldorf – Düsseldorf, Germany |
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