| Vol. 12.39 – 5 October, 2021 |
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| Researchers showed that deletion of autophagy-inducing kinase unc-51–like autophagy activating kinase 1 (ULK1) reduced growth of cell line and patient-derived xenografted chronic myeloid leukemia cells in mouse models. [Science Translational Medicine] |
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| PUBLICATIONSRanked by the impact factor of the journal |
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| MS67 potently and selectively depleted WD40 repeat domain protein 5 (WDR5) and was more effective than WDR5 protein-protein interactions inhibitors in suppressing transcription of WDR5-regulated genes. [Science Translational Medicine] |
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| The authors showed that the efficacy of immune-stimulatory gene therapy was enhanced in mIDH1 gliomas, due to the reprogramming of the myeloid cells’ compartment infiltrating the tumor microenvironment. [Science Advances] |
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| Valine enhanced hematopoietic progenitor cell (HPC) colony formation, replating of human cord blood (CB) HPC-derived colonies, mouse bone marrow (BM) and human CB HPC survival in vitro, and ex vivo expansion of normal mouse BM HSCs and HPCs. [Leukemia] |
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| Investigators developed a zebrafish tet2 mutant through which they showed that tet2 loss led to restricted hematopoietic differentiation combined with a modest upregulation of p53, which was also characteristic of many inherited bone marrow failure syndromes. [Leukemia] |
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| Scientists show that combining TKI treatment with the small-molecule MCL1 inhibitor S63845 exerted strong synergistic antiviability and proapoptotic effects on chronic myeloid leukemia (CML) lines and CD34+ stem/progenitor cells isolated from untreated CML patients in chronic phase. [Cell Death & Disease] |
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| Researchers characterized a zebrafish smu471 mutant with hematopoietic stem/progenitor cell defects and found that sart3 was the causative gene. [Cell Death & Disease] |
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| The authors developed reproducible methods to derive, from human pluripotent stem cells, a population containing monocyte progenitors able to generate functional osteoclast cells. Within this population, they identified cells with monocyte and osteoclast progenitor activity based on CD11b and CD14 expression. [Blood Advances] |
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| In acute myeloid and lymphoblastic leukemia cells, the clinical JAK inhibitors cerdulatinib, ruxolitinib and tofacitinib reduced Schlafen11 (SLFN11) expression, but interferon did not further induce SLFN11 despite phosphorylated STAT1. [iScience] |
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| The novel role of phosphatidylinositol glycan anchor biosynthesis class N (PIGN) as a regulator of the spindle assembly checkpoint was unveiled in leukemic patient cells and cell lines. [Scientific Reports] |
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| VIALE-C compared the safety and efficacy of venetoclax or placebo plus low-dose cytarabine in patients with untreated acute myeloid leukemia (AML) ineligible for intensive chemotherapy. Investigators presented an additional six months of follow-up of VIALE-C. [Blood Cancer Journal] |
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| Researchers conducted a multicenter, open-label, Phase II, single-arm study of pembrolizumab in patients with DIPSS intermediate 2 or greater primary, post-essential thrombocythemia or post-polycythemia vera myelofibrosis that were ineligible for or were previously treated with ruxolitinib. [Blood Advances] |
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| Scientists evaluated the efficacy and safety of venetoclax plus azacitidine and donor lymphocyte infusion in treating patients with relapsed acute myeloid leukemia after allogeneic hematopoietic stem cell transplantation. [Annals of Hematology] |
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| There is a rising incidence of extramedullary multiple myeloma in the era of novel agents, likely a reflection of longer overall survival (OS), with no standard treatment approach. Patients benefit from aggressive chemotherapy-based approaches, but the OS and prognosis remains poor. [Blood Cancer Journal] |
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| The authors discuss single-cell technologies that have rapidly developed over the last years and have already led to a significant impact in the research of myeloproliferative neoplasms. [Experimental Hematology] |
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| The US FDA approved brexucabtagene autoleucel for adult patients with relapsed or refractory B-cell precursor acute lymphoblastic leukemia (ALL). Efficacy was evaluated in ZUMA-3, a trial that evaluated brexucabtagene autoleucel in adults with relapsed or refractory B-cell precursor ALL. [US FDA] |
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| Senti Bio announced that it has been awarded a Small Business Innovation Research contract to support further development of SENTI-202 for acute myeloid leukemia towards clinical development. [Senti Bio] |
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| September 30 – October 1, 2021 Virtual |
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| The University of Kansas – Kansas City, Kansas, United States |
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| The University of New Mexico – Albuquerque, New Mexico, United States |
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| Moores Cancer Center, UC San Diego – San Diego, California, United States |
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| NHS Blood and Transplant – Oxford, England, United Kingdom |
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| Cellectis – Paris, France |
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