Newsletters

First in Region Innovative Cell Therapy for Synovial Sarcoma

[University of Maryland Baltimore] The University of Maryland Marlene and Stewart Greenebaum Comprehensive Cancer Center is the first in the Maryland, Delaware, Virginia, and Washington, D.C., region to offer a cell therapy treatment for patients with an advanced type of soft tissue cancer, known as synovial sarcoma.

FDA Fully Approves T-Cell Therapy for Advanced Synovial Sarcoma

[Oncology News Central] The US FDA has fully approved afamitresgene autoleucel and expanded its indication to include patients aged 12 years and older with unresectable or metastatic synovial sarcoma whose disease has progressed after chemotherapy.

MiT Fusions, TSC1-TSC2 Divergence, and Stem-Like Programs Reveal Distinct Origins, and Vulnerabilities in PEComa

[Nature Communications] Researchers performed comprehensive multi-omic profiling of an unselected perivascular epithelioid cell neoplasm cohort. Transcriptomic analysis defined four subtypes with distinct lineage programs—melanocytic, mesenchymal, or adipogenic—as well as unique mutational patterns and clinical behaviors.

The Role of the Mesenchymal Stem Cell Therapy in Bone Regeneration of Osteoporosis: Clinical Translation and Limitations

[International Immunopharmacology] In the past 20 years, MSCs have emerged as attractive treatment options for osteoporosis due to their capacity to differentiate into osteoblasts, modulate immune responses, and exert paracrine effects.

Leptin-Induced Autophagy Regulates the Immunomodulatory Potential of Adipose-Derived Mesenchymal Stem Cells through down Regulating the Expression of TSG-6

[Scientific Reports] Researchers confirmed that leptin-induced autophagy regulated the immunomodulatory potential of adipose-derived MSCs through downregulating the expression of TSG-6 via the activation of p38 pathway.

Mesenchymal Stem Cell-Mediated Delivery Boosts the Efficacy of Suicide Gene Therapy Based on Retroviral Replicating Vectors in Peritoneally Disseminated Cancer

[Cancer Gene Therapy] Scientists investigated the use of tumor-homing MSCs as retroviral replicating vectors carriers in a clinically relevant model of malignant peritoneal mesothelioma.

Mitochondrial-Derived Peptide MOTS-C Activates Metabolic Signaling but Blunts Reparative Function in Human Mesenchymal Stromal Cells

[Inflammation and Regeneration] Scientists hypothesized that restoring MOTS-c signaling rescues the impaired functionality of adipose-derived MSCs from individuals with obesity.

Amnion-Derived Mesenchymal Stem Cells Attenuate Anti-GBM Glomerulonephritis via Regulation of Neutrophil CD44 Expression

[Stem Cell Research & Therapy] Researchers focused on amnion-derived MSCs, which can be obtained non-invasively after delivery, and investigated their therapeutic effects in a rat model of anti-glomerular basement membrane nephritis.

CAV1-Dependent Mitochondrial Transfer from hucMSCs Reprograms Epithelial Lipid Metabolism to Relieve Pulmonary Fibrosis

[Stem Cell Research & Therapy] Scientists demonstrated that caveolin-1 (CAV1) enhances mitochondrial transfer from human umbilical-cord-derived MSCs to injured epithelial cells.

Mutation-Dependent Responses to Sleep and Exercise in Clonal Haematopoiesis

[Nature] In humans and mice and across mutations in Jak2, Tet2, Trp53 and Dnmt3a, researchers demonstrated mutation-dependent responses to sleep and exercise in clonal haematopoiesis and showed that mutant cells are uniquely sensitive to lifestyle.

Targeting the METTL1/M7g Axis As a Therapeutic Strategy in Myeloid Leukemia

[Blood] Scientists identified METTL1 as a key regulator of leukemia stem cell self-renewal and homing within bone marrow microenvironment through catalyzing m7G formation on a specific tRNA, tRNAPheGAA, thereby promoting leukemogenesis.

Targeting STAT3-Mediated Lipid Metabolism Reprogramming Overcomes Chemoresistance in Acute Myeloid Leukemia

[Cell Death & Disease] Researchers found that multiple lipid metabolism processes are aberrantly activated in Ara-C resistant AML cells, accompanied by upregulation of JAK-STAT3 signaling and key lipid metabolic regulators, notably SREBP1 and CPT2.
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