| Vol. 13.48 – 13 December, 2022 |
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| Researchers reported a transcriptional census of human bone-marrow-derived hematopoietic stem and progenitor cells from the neonate, infant, child, adult, and aging stages, showing two subpopulations of multipotent progenitors separated by CD52 expression. [Developmental Cell] |
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PUBLICATIONSRanked by the impact factor of the journal |
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| Scientists revealed a posttranslational regulation of kinase signaling and nuclear receptor activity via deubiquitination in T cell acute lymphoblastic leukemia. [Science Advances] |
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| Investigators analyzed the transcriptome of human HSCs purified from young and older healthy adults, as well as myelodysplastic syndromes patients, identifying transcriptional alterations following different patterns of expression. [Nature Communications] |
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| The authors interrogated the contribution of myeloid cells, the most abundant cell type in the mammalian bone marrow, in a clinically relevant mouse model of neutropenia. [Nature Communications] |
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| Scientists identified and validated a CD34dim subpopulation with hemogenic potential. They also purified CD34 cells with a CXCR4−CD73−phenotype as a definitive hemogenic endothelium population that generated HSCs and lymphocytes. [Cell Proliferation] |
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| Using zebrafish, researchers showed that hematopoietic stem and progenitor cell formation in sf3b1 homozygous mutants was dependent on STAT3 activation. [Cell Reports] |
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| Investigators delineated the role of adipocyte-CD40 in the aging hematopoietic system and evaluated the effects of adipocyte CD40 deficiency on cardiometabolic diseases. [Haematologica] |
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| Scientists investigated the expression of the FOXM1 gene in bone marrow mesenchymal stem cells (BM-MSCs) isolated from patients with myelodysplastic syndromes and AML and compared it to BM-MSCs isolated from healthy donors. [Scientific Reports] |
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| The authors compared the genetics, transcriptional profile, and clinical outcome of therapy-related NPM1-mutated AML, de novo NPM1-mutated AML, and therapy-related AML with wild-type NPM1. [Blood] |
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| Deleterious germline DDX41 variants confer risk for myeloid neoplasms (MNs), and less frequently to lymphoid malignancies, with autosomal dominant inheritance and an estimated prevalence of 3% among MNs. [Blood] |
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| Investigators summarize the emerging mechanisms of resistance to venetoclax treatment, discuss the promising combination strategies, and highlight the combinations that are currently in clinical trials. [Science Translational Medicine] |
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| In addition to treatment with CNS-penetrant systemic therapy, intrathecal prophylaxis is indicated in all patients with acute lymphoblastic leukemia, however, is not uniformly administered in patients with AML without high-risk features. [Current Treatment Options in Oncology] |
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| The US National Institutes of Health (NIH) has released a tentative plan to change how its research grant applications are scored, with the aim of reducing bias and lowering the burden on reviewers. [Nature] |
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| February 19 – 22, 2023 New Orleans, Louisiana, United States |
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| University Health Network – Toronto, Ontario, Canada |
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| University of Oxford – Oxford, England, United Kingdom |
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| Stanford University – Stanford, California, United States |
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| Bristol Myers Squibb – Uxbridge, England, United Kingdom |
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| RWTH Aachen University – Aachen, Germany |
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