| Vol. 13.40 – 11 October, 2022 |
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| Researchers explored defective hematopoiesis and provided novel insights regarding the pathogenesis of immune thrombocytopenia using bone marrow CD34+ hematopoietic stem and progenitor cells. [Signal Transduction and Targeted Therapy] |
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| PUBLICATIONSRanked by the impact factor of the journal |
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| Scientists reported that global disruption of both IRP1 and IRP2 in adult mice impaired neutrophil development and differentiation in the bone marrow, yielding immature neutrophils with abnormally high glycolytic and autophagic activity, resulting in neutropenia. [Science Advances] |
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| Non-viral sepsis upregulated IFITM3, an interferon-responsive gene that restricts viral replication. Since it was found linked to clathrin-mediated endocytosis, researchers examined if IFITM3 promoted endocytosis of alpha granule proteins. [Journal of Clinical Investigation] |
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| By exploiting the TCGA dataset, scientists found that DIS3 played a prominent role in the DNA damage response where inactivation in myeloma drove tumorigenesis via DNA:RNA hybrid-dependent enhanced genome instability and increased mutational rate. [EMBO Journal] |
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| Researchers presented that Nemp1 knockout mice showed peripheral blood defects, anemia in neonates, ineffective erythropoiesis, splenomegaly, and stress erythropoiesis. [PLoS Biology] |
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| Scientists investigated the function of Tal1 and its binding partners using a mouse embryonic stem cell-based differentiation system to model hematopoietic development and hematopoietic stem and progenitor cell generation. [Scientific Reports] |
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| This multicenter Phase IIb study aimed to investigate the efficacy and safety of tucidinostat, 40 mg twice per week, in patients with relapsed/refractory peripheral T cell lymphoma. [Haematologica] |
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| Scientists reported findings from the dose-escalation part of STIMULUS-AML1 treatment with sabatolimab+venetoclax+azacitidine to test whether it improved ND-AML patient outcomes in comparison to Phase Ib responses with sabatolimab+hypomethylating agent treatment. [Clinical Lymphoma Myeloma & Leukemia] |
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| Investigators discuss recent insights into the biology of TP53-mutated myelodysplastic syndrome and AML, current treatments, and emerging therapies, including immunotherapeutic and nonimmune-based approaches for this entity. [Cancer Discovery] |
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| The authors summarize recent research on 10-11 translation dioxygenases (TETs) in regulating both normal and pathogenic hematopoiesis, as well as the concomitant mutations and aberrant signals in TET2-mutant malignancies. [Journal of Experimental & Clinical Cancer Research] |
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| Tampa General Hospital Cancer Institute established an adult Bone Marrow Transplant and Cell Therapies unit that focused on treating patients with aggressive blood cancers such as leukemias, lymphomas, multiple myeloma as well as other cancers. [Tampa General Hospital] |
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| Mustang Bio, Inc. announced its first patient to be treated in its Phase I/II clinical trial evaluating the safety and efficacy of MB-106, their first-in-class CD20-targeted, autologous chimeric antigen receptor T (CAR T) cell therapy for relapsed or refractory B-cell non-Hodgkin lymphomas and chronic lymphocytic leukemia. [Mustang Bio, Inc.] |
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| November 6 – 8, 2022 Seville, Spain |
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| Baylor College of Medicine – Houston, Texas, United States |
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| Blood Centre of Wisconsin – Milwaukee, Wisconsin, United States |
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| CancerCare Manitoba Research Institute – Winnipeg, Manitoba, Canada |
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| University of Miami – Miami, Florida, United States |
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| Baylor College of Medicine – Houston, Texas, United States |
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