| Vol. 13.00 – 4 January, 2022 |
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| Researchers performed targeted next-generation sequencing, immunohistochemistry for MYC, BCL2, and FN1, and fluorescent multiplex immunohistochemistry for microenvironmental markers in a large cohort of diffuse large B cell lymphoma. [Clinical Cancer Research] |
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PUBLICATIONSRanked by the impact factor of the journal |
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| Using isogenic SF3B1 wild-type and mutant cell lines, normal human CD34 cells, and myelodysplastic syndrome patient cells, the authors defined a previously unrecognized role of the kinase MAP3K7, encoded by a known mutant SF3B1-targeted transcript, in controling proper terminal erythroid differentiation. [Proceedings of the National Academy of Sciences of the United States of America] |
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| Scientists found that selective AMP-activated protein kinase (AMPK)-activating compounds killed acute myeloid leukemia (AML) cells by rewiring mitochondrial metabolism that primed mitochondria to apoptosis by BH3 mimetics, holding therapeutic promise in AML. [Cell Reports] |
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| Researchers showed that HematoMiRs and their combinations targeting over 50 factors involved in HSC quiescence could induce robust ex vivo murine and human HSC expansion. In particular, HematoMiR-5 treatment enhanced cell cycle through down-regulation of negative cell cycle regulators in HSCs. [Cellular and Molecular Life Sciences] |
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| The authors showed that in T cell acute lymphoblastic leukemia cells, growth factor independence-1 (GFI1) and IKAROS were transcriptional partners that co-occupied regulatory regions of hallmark T cell development genes. [Molecular Cancer Research] |
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| Scientists showed the molecular and cellular mechanisms of lenalidomide resistance in multiple myeloma. In a comparison between lenalidomide-resistant cell lines and the parental cell lines, the extracellular vesicle secretion and adherence abilities were significantly elevated in the resistant cells. [Blood Advances] |
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| Investigators retrospectively collected the clinical data of 48 patients with mixed-lineage leukemia (MLL)-partial tandem duplications (PTD) acute myeloid leukemia or myelodysplastic syndrome with excess blasts who underwent allogeneic hematopoietic stem cell transplantation (HSCT). [BMC Cancer] |
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| The authors analyzed the level of CD33 expression in patients with newly diagnosed acute myeloid leukemia and determined its correlation with clinical characteristics. Of the 86 patients, CD33-high was closely related to the patients with normal karyotype, high white blood cell count, and a high ratio of primitive cells. [BMC Cancer] |
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| | The safety and efficacy of blinatumomab, a CD3/CD19-directed bispecific T cell engager molecule, for treatment of pediatric relapsed/refractory B cell precursor acute lymphoblastic leukemia were examined in an open-label, single-arm, expanded access study (RIALTO). [Blood Advances] |
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| In this first clinical, phase I, dose-escalation and -expansion study, scientists evaluated CC-90002 in patients with relapsed/refractory acute myeloid leukemia or high-risk myelodysplastic syndromes. [Annals of Hematology] |
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| The authors summarize the literature on post-hematopoietic stem cell transplantation immune-mediated anemia with a focus on ABO and non-ABO blood group incompatibility, describe the underlying mechanism of anemia, and outline preventive and treatment approaches. [Blood Advances] |
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| Scientists present a summary and discussion of the implications of new approaches to improve hematopoietic stem cell transplantation-based therapy. [Experimental Hematology] |
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| Celularity, Inc. announced the FDA has granted Fast Track Designation for its non-genetically modified cryopreserved human placental HSC-derived natural killer cell therapy, CYNK-001, in development for the treatment of acute myeloid leukemia (AML). [Celularity, Inc.] |
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| Daiichi Sankyo Company, Limited announced that it has submitted a New Drug Application to Japan’s Ministry of Health, Labour and Welfare for valemetostat, a potential first-in-class dual inhibitor of EZH1 and EZH2, for the treatment of patients with relapsed/refractory adult T cell leukemia/lymphoma. [Daiichi Sankyo Company, Limited] |
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| February 5 – 9, 2022 Maui, Hawaii, United States |
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| Baylor College of Medicine – Houston, Texas, United States |
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| Memorial Sloan Kettering – New York City, New York, United States |
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| Dana-Farber Cancer Institute – Boston, Massachusetts, United States |
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| The University of Texas Southwestern Medical Center – Dallas, Texas, United States |
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| Dana-Farber Cancer Institute – Boston, Massachusetts, United States |
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