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98 items found for "Pathway"

  • Unveiling Non-Canonical Functions for Gαq Signaling Pathways

    Sponsors GPCR Retreat Program < Back to schedule Unveiling Non-Canonical Functions for Gαq Signaling Pathways Ribas has characterized the existence of a new signaling pathway with a relevant role in cardiac hypertrophy

  • Context-dependent ciliary regulation of hedgehog pathway repression in tissue morphogenesis

    < GPCR News < GPCRs in Oncology and Immunology Context-dependent ciliary regulation of hedgehog pathway In the hedgehog pathway, bifunctional GLI transcription factors generate both GLI-activators (GLI-A) However, how these counterregulatory effectors coordinate cilia-regulated morphogenetic pathways is unclear Here we determined GLI-A/GLI-R requirements in phenotypes arising from lack of hedgehog pathway repression We studied hedgehog pathway repression by the GPCR GPR161, and the ankyrin repeat protein ANKMY2 that

  • GPR56 signaling pathway network and its dynamics in the mesenchymal transition of glioblastoma

    < GPCR News < GPCRs in Oncology and Immunology GPR56 signaling pathway network and its dynamics in the mining of the molecular events plausibly associated with GPR56 activity, we have constructed a signaling pathway others associated with Wnt, integrin, calcium signaling, growth factors, and inflammation signaling pathways We also considered intracellular and extracellular factors that may influence the activity of the pathway Raksha A Ganesh , Krishnan Venkataraman , Ravi Sirdeshmukh Tags GPR56 /ADGRG1 , Mesenchymal transition , Pathway

  • Transcriptomic analysis of human cytomegalovirus to survey the indirect effects on renal transplant recipients

    Methods: To investigate the activated biological pathways in HCMV infection, total RNA was extracted Afterward, Gene Ontology (GO) and pathway enrichment analyses were conducted to determine the enriched pathways and biological processes by DEGs. KEGG pathway analysis revealed the enrichment of DEGs in IL18 signaling, AGE-RAGE signaling pathway in The expression levels of six genes involved in enriched pathways including F3, PTX3, ADRA2B, GNG11, GP9

  • Dynamic Phosphoproteomics of BRS3 Activation Reveals the Hippo Signaling Pathway for Cell Migration

    in Oncology and Immunology Dynamic Phosphoproteomics of BRS3 Activation Reveals the Hippo Signaling Pathway revealed that 27 phosphopeptides corresponding to six proteins were involved in the Hippo signaling pathway Verification experiments demonstrated that downregulation of the Hippo signaling pathway caused by BRS3 demonstrate that BRS3 activation contributes to cell migration through downregulation of the Hippo signaling pathway

  • Investigating isoform switching in RHBDF2 and its role in neoplastic growth in breast cancer

    ., either they are involved in negative regulation of EGFR ligands via the ERAD pathway or positively regulate EGFR ligands via the EGFR signalling pathway. However, pathways leading to TACE-dependent EGFR signalling pathways were more observant, specifically MAPK signalling pathways, GPCR signalling pathways, and toll-like receptor pathways. and cytoplasmic ribosomal protein pathways were significantly enriched.

  • RGS20 promotes non-small cell lung carcinoma proliferation via autophagy activation and inhibition of the PKA-Hippo signaling pathway

    cell lung carcinoma proliferation via autophagy activation and inhibition of the PKA-Hippo signaling pathway Furthermore, Transcriptome sequencing was performed to show enrichment genes and pathways. Western blotting demonstrated different expressions of autophagy and the Hippo-PKA signal pathway. overexpression of RGS20 affect the proliferation and autophagy of NSCLC through regulating the Hippo pathway Transcriptomic sequencing suggested the involvement of the Hippo signaling pathway in the action of RGS20

  • GPR68-ATF4 signaling is a novel prosurvival pathway in glioblastoma activated by acidic extracellular microenvironment

    < GPCR News < GPCRs in Oncology and Immunology GPR68-ATF4 signaling is a novel prosurvival pathway in hallmark of GBM is a highly acidic tumor microenvironment, which is thought to activate pro-tumorigenic pathways specific small molecule inhibitor of GPR68 named Ogremorphin (OGM) to induce the iron mediated cell death pathway To determine GPR68 inhibition's mechanism of cell death we use DAVID pathway analysis of RNAseq.

  • Glucose and HODEs regulate Aspergillus ochraceus quorum sensing through the GprC-AcyA pathway

    and Immunology Glucose and HODEs regulate Aspergillus ochraceus quorum sensing through the GprC-AcyA pathway Here we show that the G protein-coupled receptor (GPCR) to cAMP pathway is responsible for transmitting Moreover, the GprC that classified as sugar sensor, and intracellular adenylate cyclase (AcyA)-cAMP-PKA pathway These studies highlight a crucial G protein signaling pathway for cell communication that is mediated

  • "Have a nice weekend, and I'll see you tomorrow!": RAMP-interacting GPCR Pathways

    : RAMP-interacting GPCR Pathways Date & Time Thursday, November 2nd / 4:30 PM Keynote Talk Abstract Coming

  • Comparative Analysis of the GNAI Family Genes in Glioblastoma through Transcriptomics and Single-Cell Technologies

    Hence, identifying the crucial pathways and biomarkers for the treatment of GBM is of prime importance We conducted this study to identify the pathways associated with GBM. analyses were conducted to explore the role of GNAI3 in co-expressed genes and associated signaling pathways Notable pathways included "Cytoskeleton remodeling regulation of actin cytoskeleton organization by the kinase effectors of Rho GTPases" and "Immune response B cell antigen receptor (BCR) pathway".

  • Wnt pathway inhibition with the porcupine inhibitor LGK974 decreases trabecular bone but not fibrosis in a murine model with fibrotic bone

    < GPCR News < GPCRs in Oncology and Immunology Wnt pathway inhibition with the porcupine inhibitor LGK974 Gs-GPCR signaling, suggesting that targeting the Gs-GPCR or components of the downstream signaling pathway The Wnt signaling pathway has been implicated in the pathogenesis of FD-like bone, but the specific Wnts insights into the role of Wnt and Gs-signaling in fibrosis and bone formation in a mouse model of Gs-GPCR pathway Tania Moody, Ariane Zamarioli, Apsara Ram, Gauri Ganesh, Misun Kang, Sunita Ho, Edward C Hsiao Tags Wnt pathway

  • Ep 132 with Dr. Richard Premont

    GRKs (particularly GRKs 4,5,6) and arrestins as GPCR regulators and as mediators of distinct signaling pathways position at Duke in Gastroenterology, where he remained until 2018 studying GPCRs and their signaling pathways My research focus is on understanding how distinct cellular signaling pathways interact and are coordinated system, the coordination of heterotrimeric G protein, small GTP-binding protein and protein kinase pathways S-nitrosylation as a signaling post-translational modification in mediating and regulating cellular signaling pathways

  • Ep 130 with Dr. Richard Premont

    GRKs (particularly GRKs 4,5,6) and arrestins as GPCR regulators and as mediators of distinct signaling pathways position at Duke in Gastroenterology, where he remained until 2018 studying GPCRs and their signaling pathways My research focus is on understanding how distinct cellular signaling pathways interact and are coordinated system, the coordination of heterotrimeric G protein, small GTP-binding protein and protein kinase pathways S-nitrosylation as a signaling post-translational modification in mediating and regulating cellular signaling pathways

  • Ep 133 with Dr. Richard Premont

    GRKs (particularly GRKs 4,5,6) and arrestins as GPCR regulators and as mediators of distinct signaling pathways position at Duke in Gastroenterology, where he remained until 2018 studying GPCRs and their signaling pathways My research focus is on understanding how distinct cellular signaling pathways interact and are coordinated system, the coordination of heterotrimeric G protein, small GTP-binding protein and protein kinase pathways S-nitrosylation as a signaling post-translational modification in mediating and regulating cellular signaling pathways

  • Ep 131 with Dr. Richard Premont

    GRKs (particularly GRKs 4,5,6) and arrestins as GPCR regulators and as mediators of distinct signaling pathways position at Duke in Gastroenterology, where he remained until 2018 studying GPCRs and their signaling pathways My research focus is on understanding how distinct cellular signaling pathways interact and are coordinated system, the coordination of heterotrimeric G protein, small GTP-binding protein and protein kinase pathways S-nitrosylation as a signaling post-translational modification in mediating and regulating cellular signaling pathways

  • Stimulation of ectopically expressed muscarinic receptors induces IFN-γ but suppresses IL-2 production by inhibiting activation of pAKT pathways in primary T cells

    muscarinic receptors induces IFN-γ but suppresses IL-2 production by inhibiting activation of pAKT pathways phosphorylation of downstream signaling molecules and the phosphatidylinositol, Ras, MAPK, and PI3 kinase pathways G-protein-coupled human muscarinic receptor could bypass tyrosine kinases to activate the phosphatidylinositol pathway Interestingly, stimulation of hM3Dq resulted in reduced pAKT and its downstream pathway. reduced IL-2 production in TCR-stimulated hM3Dq/β1 CD4 T cells, suggesting that activating the pAKT pathway

  • Systems modeling of oncogenic G-protein and GPCR signaling reveals unexpected differences in downstream pathway activation

    Systems modeling of oncogenic G-protein and GPCR signaling reveals unexpected differences in downstream pathway mutations, and our experiments confirmed oncogenic CysLT2R was impaired at activating the FAK/YAP/TAZ pathway our bioinformatic analysis uncovers a role for co-occurring mutations involving the plexin/semaphorin pathway , which has been shown capable of activating this pathway.

  • Systems Pharmacodynamic Model of Combination Gemcitabine and Trabectedin in Pancreatic Cancer Cells. Part II: Cell Cycle, DNA Damage Response, and Apoptosis Pathways

    Part II: Cell Cycle, DNA Damage Response, and Apoptosis Pathways Published date October 31, 2023 Abstract related to cell growth and migration, specifically the RTK-, integrin-, GPCR-, and calcium-signaling pathways Here we describe drug effects on pathways associated with cell cycle, DNA damage response (DDR), and Drug combination effects on protein changes in the cell cycle- and apoptosis pathways contribute to the

  • Session VII | Adhesion GPCR Workshop 2024 | Dr. GPCR Ecosystem

    Session VII Physiological and pathological roles of AGPCRs in the nervous system Uncovering the signaling pathway Remoulade in Drosophila Beatriz Blanco Redondo The Adhesion GPCR Latrophilin Interacts With The Notch Pathway To Control Germ Cell Proliferation Willem Berend Post Uncovering the signaling pathway of the ADGRA We also aimed at identifying the signaling pathway that Remo is involved in. Remo may serve a role in this peculiar signaling pathway and require further analysis."

  • Vasoactive intestinal peptide receptor 2 signaling promotes breast cancer cell proliferation by enhancing the ERK pathway

    intestinal peptide receptor 2 signaling promotes breast cancer cell proliferation by enhancing the ERK pathway cAMP and phosphorylated extracellular signal-regulated kinase (ERK), which involves a VIPR2 signaling pathway these findings suggest that VIPR2 controls breast tumor growth by regulating the cAMP/PKA/ERK signaling pathway

  • GPR143 controls ESCRT-dependent exosome biogenesis and promotes cancer metastasis

    controls the endosomal sorting complex required for the transport (ESCRT)-dependent exosome biogenesis pathway quantitative proteomic and RNA profiling of exosomes in human cancer cell lines showed that the GPR143-ESCRT pathway metastasis by secreting exosomes and increasing cancer cell motility/invasion through the integrin/FAK/Src pathway

  • Activation of PI3K/Akt pathway by G protein-coupled receptor 37 promotes resistance to cisplatin-induced apoptosis in non-small cell lung cancer

    < GPCR News < GPCRs in Oncology and Immunology Activation of PI3K/Akt pathway by G protein-coupled receptor cisplatin, and affects tumor formation and growth. (3) GPR37 activates PI3K/Akt/mTOR signal transduction pathways , Jing Jie , Shucheng Hua , Xiaoxue Bai , Shuai Wang , Lei Song Tags EMT , GPR37 , NSCLC , PI3K/Akt pathway

  • Prediction of survival and immunotherapy response by the combined classifier of G protein-coupled receptors and tumor microenvironment in melanoma

    analysis, bioinformatic analysis and luciferase assays were performed to establish a potential signaling pathway over-expression of miR-19a could regulate the signaling between GRK6, GPR39 and PKC via the signaling pathway development of innovative therapeutic interventions aimed at regulating GRK6 and its downstream signaling pathways

  • Ep 82 with Dr. Lauren M. Slosky

    Because BAMs engage less well-conserved allosteric sites and exert pathway-specific effects on receptor signaling, they are exciting tools for linking distinct signaling pathways with their physiological Yamamura Endowed Fellowship in Pharmacology, an NIH F32 Postdoctoral Fellowship, and an NIH K99/R00 Pathway

  • Ep 92 with Dr. Stephane Angers

    Moon , where he identified and characterized novel components of the Wnt signaling pathway and a new His pioneer work led to the development of novel antibody molecules blocking and activating the Wnt pathway

  • GPR37 expression as a prognostic marker in gliomas: a bioinformatics-based analysis

    GPR37 is an orphan G protein-coupled receptor (GPCR) that is implicated in different physiological pathways regulation of macrophage derived foam cell differentiation, negative regulation of T cell receptor signaling pathway , neuroactive ligand receptor interaction, calcium signaling pathway, and negatively associated with

  • GPR97 depletion aggravates imiquimod-induced psoriasis pathogenesis via amplifying IL-23/IL-17 axis signal pathway

    depletion aggravates imiquimod-induced psoriasis pathogenesis via amplifying IL-23/IL-17 axis signal pathway

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