The hub genes (VGF, DGKD, and C19orf52) of neuroblastoma are screened. VGF, one of the hub genes, may have a high diagnostic value and is involved in the immune cell infiltration in neuroblastoma tissue, which may be used as a biomarker for the diagnosis of neuroblastoma and provides a new direction for clinical prognosis prediction and management improvement.
These findings underscore the pivotal and isoform-specific involvement of DGKs in AML, offering a promising pathway for the identification of potential therapeutic targets. Notably, the DGKA and DGKH isoforms emerge as relevant players in AML pathogenesis, albeit DGKA inhibition alone seems insufficient to impair AML cell viability.
We detected 3 novel fusion genes (SFMBT2::DGKD, PDS5B::STAG2, and TDRD5::LPCAT2), for which the sequence and expression were validated by long-read and whole transcriptome sequencing, respectively. OGM and WES identified double hits of SVs and SNVs (ETV6, BTG1, STAG2, MANBA, TBL1XR1, NSD2) in the same patient demonstrating the power of the combined approach to define the landscape of genomic alterations in BCP-ALL.
over 2 years ago
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CDKN2A (Cyclin Dependent Kinase Inhibitor 2A) • RUNX1 (RUNX Family Transcription Factor 1) • ETV6 (ETS Variant Transcription Factor 6) • IKZF1 (IKAROS Family Zinc Finger 1) • PAX5 (Paired Box 5) • STAG2 (Stromal Antigen 2) • CD4 (CD4 Molecule) • DGKD (Diacylglycerol Kinase Delta) • DRD5 (Dopamine Receptor D5) • GPRC5A (G Protein-Coupled Receptor Class C Group 5 Member A) • IKBKB (Inhibitor Of Nuclear Factor Kappa B Kinase Subunit Beta) • LPCAT2 (Lysophosphatidylcholine Acyltransferase 2) • NSD2 (Nuclear Receptor Binding SET Domain Protein 2) • SFMBT2 (Scm Like With Four Mbt Domains 2) • TBL1XR1 (TBL1X Receptor 1)
Moreover, Doxorubicin was identified by Connectivity Map website with the differential malignant progression-related genes. CCK-8 assay, Edu assay, wound healing assay, and trans-well experiment were used to reveal that Doxorubicin could inhibit proliferation, migration and invasion of IOMM-Lee Cells.
almost 3 years ago
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MIR664A (MicroRNA 664a) • DGKD (Diacylglycerol Kinase Delta) • NSD2 (Nuclear Receptor Binding SET Domain Protein 2)
Our study reveals that the resistance to TKIs (pazopanib or sunitinib) occurs by increasing vasculogenic mimicry (VM) ability to counteract the TKI angiogenesis suppression function. Furthermore, we find a potential therapy to more effectively treat TKI resistant RCC by blocking ERβ/circRNA-DGKD/miR-125-5p/VE-cadherin pathway together with pazopanib administration.
The model had good predictive power for the WT prognosis at 1, 3, and 5 years (AUC: 0.684, 0.762, and 0.774). Finally, ERRFI1 (hazard ratios [HR] = 1.858, 95% confidence intervals [CI]: 1.298-2.660) and ROR1 (HR = 0.780, 95% CI: 0.609-0.998) were obtained as independent predictors of prognosis in WT patients by single, multifactorial Cox analysis.