| Vol. 13.11 – 22 March, 2022 |
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| In models of AML, leukemia cell differentiation and therapeutic benefit mediated by the histone deacetylases inhibitor panobinostat required activation of the type I interferon pathway. [Cancer Discovery] |
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PUBLICATIONSRanked by the impact factor of the journal |
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| Investigators found that HSCs temporally transitioned to depend on thrombopoietin, a key extrinsic factor, from E16.5 onward in the developing liver. [Science Advances] |
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| The role of wild-type isocitrate dehydrogenase-2 (IDH2) in AML cell survival and proliferation was tested using genetic knockdown and pharmacological inhibition in AML cells and animal models. [Journal of Hematology & Oncology] |
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| The authors established cells with acquired resistance to the allosteric SHP2 inhibitor SHP099 from two FLT3-ITD-positive AML cell lines. [Cancer Research] |
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| Investigators found that AML cells obtained from relapsed patients had increased autophagy levels than de novo AML cells. [Haematologica] |
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| Scientists used Sanger sequencing of commonly mutated genes and a custommade targeted next-generation sequencing panel covering 226 genes known to be mutated in inherited cytopenias; the minority subsequently underwent whole exome sequencing. [Haematologica] |
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| The authors demonstrated that DDX41 was required for mouse HSC and progenitor cell survival and differentiation, particularly of myeloid lineage cells. [Stem Cell Reports] |
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| Investigators found that AML cells released a heterogeneous population of extracellular vesicles containing microRNAs involved in AML pathogenesis. [Frontiers in Oncology] |
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| To explore the efficacy of sorafenib combined with conventional therapies for refractory central nervous system leukemia, a Phase II study was conducted. [Cancer] |
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| Researchers systematically conducted a comparative plasma proteomic profiling on β-thalassemia patients and healthy controls. Among 246 dysregulated proteins, 13 core protein signatures with excellent biomarker potential were proposed. [iScience] |
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| Recent clinical successes for gene therapies involving autologous HSC transplantation demonstrate the potential of genetic engineering in this stem cell type for curing disease. [Nature Reviews Immunology] |
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| The author reviews some of the key pathways including the infectious and inflammatory processes that control hematopoiesis, followed by a comprehensive review that summarizes the latest evidence and discusses how SARS-CoV-2 infection impacts hematopoiesis. [Cellular and Molecular Life Sciences] |
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| Scientists summarize the potential miRNAs, especially circulating ones, involved in essential signaling pathways in acute lymphocytic leukemia and chronic lymphocytic leukemia patients which serve as biomarkers and valuable targets in the treatment fields. [Journal of Cellular Physiology] |
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| Wugen, Inc. announced that the first patient has been dosed in a Phase I/II trial of WU-CART-007 for the treatment of relapsed or refractory (R/R) T cell acute lymphoblastic leukemia (T-ALL)/lymphoblastic lymphoma (LBL). [Wugen, Inc.] |
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| Oryzon Genomics, S.A. announced that it has received notification from the US FDA that its Investigational New Drug application (IND) for iadademstat is now approved to initiate a Phase Ib clinical trial in patients with relapsed/refractory (R/R) AML harboring a FMS-like tyrosine kinase mutation (FLT3mut+ ). [Oryzon Genomics, S.A.] |
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| University Children’s Hospital of Zurich – Zurich, Switzerland |
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| University of Illinois Chicago – Chicago, Illinois, United States |
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| Wellcome Sanger Institute – Cambridge, United Kingdom |
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| The University of California, Davis – Davis, California, United States |
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| TU Dresden – Dresden, Germany |
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