| Vol. 12.46 – 23 November, 2021 |
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| Scientists reported that the risk of donor cell leukemia in allogeneic hematopoietic cell transplantation was driven by somatic myelodysplastic syndrome–associated mutations or germline predisposition in donors. [Journal of Clinical Oncology] |
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PUBLICATIONSRanked by the impact factor of the journal |
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| Investigators performed dense, daily, temporal profiling of chromatin accessibility and gene expression changes along ex vivo human erythropoiesis to comprehensively define developmentally regulated DNase I hypersensitive sites and transcripts. [Nature Communications] |
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| The authors showed that AT-rich interaction domain 4B (ARID4B) interfered with KITLG/KIT signaling, consequently allowing HSC differentiation. Conditional Arid4b knockout in mouse hematopoietic cells blocked fetal HSC differentiation, preventing hematopoiesis. [Cell Reports] |
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| Researchers performed cytogenetic, single nucleotide polymorphism array and next generation sequencing analyses on samples from 210 patients aged above 60 years from the UKALL14 and UKALL60+ clinical trials. [Haematologica] |
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| Using Ixodes ovatus Ehrlichia, a tick-borne pathogen that causes severe shock-like illness and bone marrow aplasia, type I and II interferons promoted the loss of hematopoietic stem and progenitor cells via increased cell death and enforced quiescence. [Stem Cell Reports] |
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| Scientists identified CD62L as a marker to reveal the heterogeneity within progenitors. They confirmed that CD62L-negative common myeloid progenitors (CMPs) represented “bona fide” CMPs, and CD62L-high CMPs were mostly restricted to granulocyte-monocyte progenitors potentials in mice and humans. [Stem Cell Reports] |
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| The authors investigated the anti-adult T cell leukemia/lymphoma effects of a novel oral HSP90 inhibitor TAS-116 and the mechanisms involved in ex vivo and in vivo preclinical models. [Cancer Science] |
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| Researchers revealed the breadth of SWI/SNF dependency in leukemia and supported targeting SWI/SNF catalytic function as a potential therapeutic strategy in acute myeloid leukemia. [Molecular Cancer Research] |
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| Scientists generated ex vivo drug response and multi-omics profiling data for a prospective series of 252 samples from 186 acute myeloid leukemia patients. Functional precision medicine tumor board integrated clinical, molecular and functional data for application in clinical treatment decisions. [Cancer Discovery] |
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| The authors introduced multiple myeloma-patient similarity network, the first multiomics patient similarity network of myeloma that enabled accurate dissection of the genetic and molecular landscape of the disease and determined 12 distinct subgroups defined by five data types. [Science Advances] |
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| Investigators evaluated the usefulness of plasma concentration of circulating mir-146a as a non-invasive biomarker for acute lymphoblastic leukemia. Total RNA including miRNA was isolated from 110 plasma samples of patients, healthy controls, and follow up cases and reverse transcribed. [Scientific Reports] |
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| Scientists discern the circular RNAs’ evolving role in elucidating acute myeloid leukemia (AML) biology and therapy resistance and attempt to identify its potential in managing AML. [Molecular Cancer] |
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| The authors present a few actionable steps for basic, translational and clinical research communities in advancing the utility of the platelet transcriptome as a highly sensitive biomarker in cancer and collectively enable efforts toward clinical translation and patient benefit. [British Journal of Cancer] |
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| Investigators briefly review the challenges of treating acute myeloblastic leukemia with a glance at the extracellular vesicles’ role in this process. [Leukemia Research] |
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| Apollomics, Inc. announced that the first patient has been successfully dosed in a Phase III clinical trial of APL-106 for the treatment of adults with relapsed or refractory acute myeloid leukemia in China. [Apollomics, Inc.] |
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| Graphite Bio, Inc. announced that the first patient has been enrolled in the company’s Phase I/II clinical trial of GPH101, an investigational gene-edited autologous hematopoietic stem cell therapy designed to directly correct the genetic mutation that causes sickle cell disease. [Graphite Bio, Inc.] |
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| December 11 – 14, 2021 Atlanta, Georgia, United States |
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| Dana-Farber Cancer Institute – Boston, Massachusetts, United States |
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| Karolinska Institutet – Flemingsberg, Sweden |
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| Dana-Farber Cancer Institute – Boston, Massachusetts, United States |
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| Icahn School of Medicine at Mount Sinai – New York, New York, United States |
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Boston Children’s Hospital – Boston, Massachusetts, United States |
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