RT-qPCR results further confirmed differential expression patterns of the 8 genes between normal and GBM cells, supporting their involvement in GBM pathogenesis. This 8-gene risk model effectively predicts glioma prognosis and supports personalized treatment strategies by highlighting immune microenvironment differences and drug sensitivities between risk groups.
3 months ago
Journal • Gene Signature
|
GADD45G (Growth Arrest And DNA Damage Inducible Gamma) • GRIK2 (Glutamate Ionotropic Receptor Kainate Type Subunit 2) • RBP1 (Retinol Binding Protein 1)
We inferred cell-state-specific communication in various cell types. Our findings provide potential targets such as Slit2-Robo 1/2, Gabrg3, Gabra2, Grm4, Grik2, Cadps2 and Camk4 on therapeutic strategies for neuropathic or orofacial pain.
The landscape of cytokines, checkpoint ligands and receptors uncovered Mrc1, PD-L1, TIM-3 or B7-H3, among the immunotherapy targets that can be addressed in this model. The comparison with human GBMs unveiled crucial similarities with TMEMed GBM, the most frequent subtype.
This case suggests that involuntary movements and psychiatric symptoms may represent novel phenotypes of anti-GluK2 antibody-associated autoimmune encephalitis. The findings underscore the importance of recognizing the diverse clinical presentations of this rare condition and prompt further research into its underlying mechanisms.
1 year ago
Journal
|
GRIK2 (Glutamate Ionotropic Receptor Kainate Type Subunit 2)
Cerebellar ataxia in NMDAR-E may not be explained by concomitant KLHL11, MOG, AQP-4, or GluK2 autoimmunity. Of note, ataxia in NMDAR-E may result from treatment complications and, most interestingly, from MS manifesting in temporal association with NMDAR-E.
1 year ago
Observational data • Journal
|
GRIK2 (Glutamate Ionotropic Receptor Kainate Type Subunit 2)
The intravenous methylprednisolone, immunoglobulin, antibiotics and other symptomatic treatments helped the patient to recover full...Our report provides more evidence that anti-GluK2 antibodies may be pathogenic for the autoimmune encephalitis (cerebellitis). Immunotherapy can be used to treat it with good outcome.
And novel immunotherapy and chemotherapy regimens were accordingly proposed for the elderly LUAD patients. We identified a novel gene signature based on seven ARGs for risk stratification, prognosis prediction and benefit evaluation of immunotherapy and chemotherapy in elderly LUAD patients.
over 1 year ago
Journal • IO biomarker
|
DKK1 (dickkopf WNT signaling pathway inhibitor 1) • CD79A (CD79a Molecule) • CDX2 (Caudal Type Homeobox 2) • COL1A1 (Collagen Type I Alpha 1 Chain) • CDK3 (Cyclin Dependent Kinase 3) • GRIK2 (Glutamate Ionotropic Receptor Kainate Type Subunit 2)
The number of antibodies against surface antigens is increasing in ACA, but the response to the immunotherapy remains suboptimal. More studies are needed to clarify the role of most of the antibodies against intracellular antigens described in these patients.
GRIK2, downregulated due to promoter hypermethylation, acted as a TC suppressor. Our 5-CpG epigenetic signature effectively discriminates lymphatic metastasis in BRAF wild-type TC, highlighting GRIK2's tumor-suppressive role influenced by promoter hypermethylation.
We administered the AAV9-vector carrying two small interfering RNAs targeting GRIK2 (AMT-260) bilaterally into the hippocampus of a mouse model for TLE (pilocarpine) and into non-human primates (NHP). With the preclinical efficacy in pharmacology models and a good safety profile, AMT-260 will proceed into clinical testing for the treatment of patients with refractory mesial temporal lobe epilepsy.
2 years ago
Preclinical
|
GRIK2 (Glutamate Ionotropic Receptor Kainate Type Subunit 2)