The hub genes act as molecular bridges connecting the observed genomic and epigenetic variations, particularly driving chromatin-related regulation and MAPK signaling pathways. In particular, PSMC1, SNW1, H3C2, H1-2, and H2BC14 genes offer promising molecular targets for future therapeutic approaches in SACs.
This study clarified FLT3 as being involved in the pathogenesis of meningioma from a genetic perspective and genetically predicted lower FLT3L to be causally associated with a higher meningioma risk, implicating FLT3 signalling in meningioma pathogenesis. FLT3 as a genetically supported candidate factor associated with meningioma risk.
The combination of Flt3L and anti-CTLA-4 enhanced therapeutic responses. Combination therapy is associated with the emergence of a CD8+ T cell subset characterized by the expression of Il21r and oligoclonal expansion of CD8+ T cells within tumors through a mechanism that is dependent on lymph node egress.
1 month ago
Journal • IO biomarker
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FLT3 (Fms-related tyrosine kinase 3) • CD8 (cluster of differentiation 8) • SLAMF6 (SLAM Family Member 6) • IL1R1 (Interleukin 1 receptor, type I) • IL21R (Interleukin 21 Receptor) • FLT3LG (Fms Related Receptor Tyrosine Kinase 3 Ligand)
This study identified several CIPs - including TNF-β, osteoprotegerin, and adenosine deaminase - as potentially causal in OM development. These findings highlight promising targets for future immunomodulatory therapies aimed at preventing or mitigating osteomyelitis.
Correlations with immune cell infiltration and checkpoint markers suggested that FLT3LG may predict enhanced responses to immune checkpoint inhibitors and certain targeted drugs. These findings support its potential as a multifunctional biomarker for prognosis and therapeutic decision making in breast cancer.
5 months ago
Journal • IO biomarker
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TP53 (Tumor protein P53) • PIK3CA (Phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha) • FLT3LG (Fms Related Receptor Tyrosine Kinase 3 Ligand)
Consistently, human CD56brightCD16- NK cells more strongly correlated with cDC1 and FLT3LG expression than other NK cell subsets across multiple human melanoma datasets and cancer indications. This mechanistic study of NK cell regulation of FLT3LG and control of the NK cell-cDC1 axis provides insights and strategies for the development of more effective cancer immunotherapies.
Boxplot analysis confirmed that Flt3L, IL-18, IL-1α, IL-7, IL-8, MCP-1, MMP-1, OPG, SCF, and VEGFA were specifically elevated in nAMD compared with both PCV and NC groups, while IL-10 was specifically suppressed in PCV. Tear fluid analysis represents a feasible and noninvasive approach to investigate the pathogenesis of PCV and nAMD.
Reverse MR suggested meningiomas might lower plasma FLT3L, C-X-C motif chemokine 11, adenosine deaminase, and hepatocyte growth factor levels. FLT3L may play a protective role in meningiomas, warranting further research on inflammatory proteins for prevention and treatment strategies.
Specifically, the results suggested that Flt3L and MCP4 may be risk factors for PCa, whereas MCP2 may be a favorable factor for PCa. Conversely, adenosine deaminase, axin-1, C-X-C motif chemokine ligand 6, IL-24, IL-33, and Flt3L were involved in the downstream of PCa progression.
The therapeutic efficacy of FX-armed chimeric antigen receptor (CAR)-T cells is further validated in the Flt3KO&hFLT3LG humanized mouse model. This strategy offers a promising avenue for enhancing DC-T cell interactions, paving the way for more effective immunotherapy against solid tumors.
7 months ago
Journal
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SLAMF6 (SLAM Family Member 6) • FLT3LG (Fms Related Receptor Tyrosine Kinase 3 Ligand)
This study identifies lipids and inflammatory markers as key mediators of HNC development, offering potential diagnostic and therapeutic targets for future research.
8 months ago
Journal
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FLT3LG (Fms Related Receptor Tyrosine Kinase 3 Ligand)
This analysis identified a blood-based 7-gene signature shared between LUAD and microbial lung infections, associated with immunosuppressive microenvironment features, suggesting a potential link between infection-driven inflammation and tumor-promoting immune modulation.
8 months ago
Journal • Gene Signature
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CD8 (cluster of differentiation 8) • BCL6 (B-cell CLL/lymphoma 6) • CD163 (CD163 Molecule) • FLT3LG (Fms Related Receptor Tyrosine Kinase 3 Ligand) • S100A12 (S100 Calcium Binding Protein A12) • RPL22 (Ribosomal Protein L22)