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Tempus and Blood Cancer United® Announce Collaboration to Develop One Of the Largest Pediatric Acute Myeloid Leukemia Real-World Data Registries
[Tempus AI, Inc.] Tempus AI, Inc., and Blood Cancer United® announced a strategic collaboration to develop a comprehensive, patient-centered, real-world registry for pediatric acute myeloid leukemia, a rare and aggressive blood cancer.
A Mechanism to Initiate Emergency Type 2 Myelopoiesis
[Nature] Researchers showed that infection with the helminth Heligmosomoides polygyrus increases erythroid-primed multipotent progenitor commitment to myeloid fate at the expense of erythropoiesis.
Pharmacological Inhibition of miR-126 Enhances Venetoclax Activity in Acute Myeloid Leukemia
[Blood] Scientists demonstrated that microRNA-126 (miR-126) maintained leukemic stem cells function by promoting B-cell lymphoma 2–dependent FAO, OXPHOS, and mitofusion, whereas its inhibition disrupts mitochondrial metabolism, induces mitochondrial fission, and triggers apoptosis.
Epigenetic Remodeling via HDAC6 Inhibition Amplifies Anti-Tumoral Immune Responses in Myeloid Leukemia Cells
[Cell Death & Disease] Researchers demonstrated that histone deacetylase 6 (HDAC6) loss significantly impairs myeloid leukemia progression in vivo, despite having no functional impact on leukemia cell proliferation in vitro.
Targeting Menin in T-Lineage Acute Lymphoblastic Leukemia
[Molecular Cancer Therapeutics] Investigators evaluated the efficacy of menin inhibition in T-lineage acute lymphoblastic leukemia (T-ALL) and identified molecular predictors of sensitivity. They tested menin inhibitors, ziftomenib, revumenib, VTP-50469, in 14 primary T-ALL samples and 8 cell lines, representing HOXA-high and HOXA-low genotypes.
Sustained MYC Overexpression Drives Myeloid Differentiation Block and Acquisition of Leukemic Phenotypes
[Experimental Hematology] The authors demonstrated that MYC overexpression from the endogenous locus, which maintains physiological regulation, results in a transient and reversible differentiation block that is insufficient for leukemogenesis.
Orca-T Vs Allogeneic Hematopoietic Stem Cell Transplantation (Precision-T): A Multicenter, Randomized Phase III Trial
[Blood] This phase III trial randomized adult patients with acute leukemias or myelodysplastic syndrome undergoing myeloablative conditioning to receive either Orca-T with tacrolimus or a conventional allograft with tacrolimus and methotrexate, using granulocyte colony-stimulating factor–mobilized peripheral blood from HLA-matched donors.
MSLN Expression Predicts a High Risk of EMD in AML by Promoting Cell Adhesion and Metastasis via Interaction with MUC16
[Blood Advances] Investigators analyzed a cohort of 118 adult patients with de novo AML, among whom 27 developed extramedullary disease (EMD) in various body sites, with tissue involvement as the most common.
Ph-Negative Acute Lymphoblastic Leukemia in the Older Adults: Biology, Therapeutic Strategies, and Unmet Needs
[European Journal of Haematology] The authors summarize the evolving treatment landscape for older patients with acute lymphoblastic leukaemia, from conventional chemotherapy to novel immunotherapeutic approaches.
Genetic Variation and Inflammation Intersections: GATA2- and RUNX1-Linked Mechanisms of Blood Pathogenesis
[Experimental Hematology] Scientists considers how inflammation triggers or amplifies the functional ramifications of conditionally pathogenic variation as a blood pathogenic mechanism, with a particular emphasis on GATA2 and RUNX1 transcription factor-linked mechanisms.
The ITGB2-COPS3-SOX2 Axis and SOX2 Liquid-Liquid Phase Separation: Dual Mechanisms Governing Osteosarcoma Stemness
[Advanced Science] High-frequency amplification of the 17p11.2 chromosomal region in osteosarcoma represents a key molecular event driving malignant progression. Investigators focused on the key gene COPS3 in this region, delving into its molecular mechanisms regulating cancer stemness.
Dual Role of LY96 in Shaping the Mesenchymal Glioblastoma Ecosystem through Stem Cell Maintenance and Macrophage MES-Like Reprogramming
[Cancer Letters] Researchers demonstrated that mesenchymal glioblastoma stem cells exhibit a preferential expression and secretion of the protein LY96.

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