Newsletters
Integration of an Anellovirus Genome in the SKNO-1 Acute Myeloid Leukemia Cell Line
[Microbiology Spectrum] Researchers identified a stably integrated and transcriptionally active anellovirus genome in anAML cell line, providing a unique model to study viral persistence in hematopoietic cells.
CD55 Promotes Hematopoietic Stem and Progenitor Cell Survival in a Mouse Model of Immune-Mediated Aplastic Anaemia
[Blood Advances] Scientists showed that CD55 protects hematopoietic stem and progenitor cells from complement-mediated damage in aplastic anemia, highlighting complement inhibition as a potential therapeutic strategy
The Fanconi Anemia Pathway Restrains MLL-Rearranged Leukemogenesis through Suppressing Non-Homologous End Joining-Mediated Genomic Instability
[Nature Communications] Using murine models and human mixed lineage leukemia (MLL)-r leukemia cells, the authors showed that the FA pathway suppresses leukemogenesis by limiting error-prone non-homologous end joining-mediated genomic instability.
Inhibition of Nucleoporin 214 Depletes Leukemia Stem Cells by Promoting Heme Catabolism and Lipid Peroxidation
[Blood] By screening the nucleoporin (NUP) family, scientists identified NUP214 as a frequently overexpressed gene and a critical fitness determinant in leukemia stem cells (LSCs). NUP214 acts as a conserved driver of LSC survival by restricting heme catabolism, limiting Fe²⁺ accumulation, and suppressing lipid peroxidation.
PTBP1 Controls Oncogenic Transcript Processing and Maintenance of Acute Myeloid Leukemia
[Leukemia] Researchers identified the RNA splicing factor PTBP1 as a key dependency in acute myeloid leukemia, sustaining leukemia by controlling the processing of essential oncogenic transcripts.
Single-Cell Architecture of Purinergic Signaling in Human Cord Blood Hematopoietic Stem and Progenitor Cells
[Leukemia] Investigators mapped purinergic signaling at single-cell resolution in human cord blood stem and progenitor cells, revealing how ATP and adenosine pathways are organized across early blood cell development.
The Role of the Adenosinergic Pathway in Resistance to Hypomethylating Agents in Patients with High-Risk Myelodysplastic Syndromes
[British Journal of Haematology] The authors investigated the expression of CD39, CD73 and related adenosinergic pathways and their clinical associations in T cells of higher-risk myelodysplastic syndromes patients undergoing hypomethylating agent therapy.
Chemotherapy-Related Anaemia Is Regulated through Caspase-1 Mediated ROCK1 Activation
[Blood Advances] Scientists showed that chemotherapy-induced anemia is driven by Caspase-1–mediated ROCK1 activation, which suppresses red blood cell production and reveals a potential therapeutic target for improving erythropoietic recovery.
Epigenetic Markers Expand Genetic Risk Estimation in Acute Myeloid Leukemia
[Blood] Researchers assessed whether DNA methylation patterns in AML patients can augment risk assessments provided by genetic and other markers to better predict outcomes
Histone Deacetylase Inhibitors As Venetoclax-Sensitising Partners in Acute Myeloid Leukaemia: Mechanisms, Pharmacology, and Translational Perspectives
[British Journal of Pharmacology] The authors discuss the rationale and evidence for combining histone deacetylase inhibitors with venetoclax in AML, including mechanisms of action, resistance pathways, and preclinical and clinical data
FDA Approves PharmaEssentia’s BESREMi® (ropeginterferon alfa-2b-njft) for Adults with Essential Thrombocythemia, A Rare Blood Cancer
[PharmaEssentia USA Corporation (Business Wire)] PharmaEssentia USA Corporation announced the US FDA has approved BESREMi® for the treatment of adults with essential thrombocythemia (ET), making it the first new FDA-approved treatment for ET in nearly three decades.
Cancer Center Physician Receives $150,000 New Investigator Research Grant to Study Treatment-Resistant Leukemia
[University of Cincinnati] The University of Cincinnati Cancer Center’s Dr. Sarah Skuli, has received a two-year, $150,000 New Investigator Research Grant from the Leukemia Research Foundation. The funds will go toward a project that focuses on leukemia carrying mutations in the TP53 gene, which leads to very poor outcomes for patients.

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