AGEs inhib 
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  • ||||||||||  Protective effect of RAGE inhibitor compound A on emphysema () -  Nov 5, 2024 - Abstract #APSR2024APSR_8;    
    These findings show that inhibiting RAGE in alveolar epithelial cells suppresses lung injury and emphysema by inhibiting oxidative stress-induced inflammation and MMPs and promoting alveolar epithelial cell proliferation. The interruption of DAMP-RAGE interaction through CA offers a promising therapeutic strategy for the alleviation of emphysema.
  • ||||||||||  Increased RAGE Expression in Myositis (In Person) -  Sep 25, 2024 - Abstract #ACRConvergence2024ACR_Convergence_2428;    
    Overall, we observed increased RAGE expression in the skeletal muscle of myositis mice and human patients. These findings suggest that RAGE inhibition may be a promising strategy to dampen inflammation, improve muscle function, and ultimately enhance patient well-being.
  • ||||||||||  Preclinical, Journal:  Phytochemical, biochemical and physiological assessment of the protective effect of local Trigonella foenum graecum in rats administered a ?-cell toxicant. (Pubmed Central) -  Sep 13, 2024   
    In vivo, 10%AFS- supplemented diet (w/w) was found to elicit a significant reduction in glycemia, TNF-?, IL-6, CRP, liver markers, lipid peroxidation (MDA) and protein carbonyl (PCO) along with improvement in reduced glutathione (GSH) amount, glutathione peroxidase (GPx), catalase (CAT) and glutathione-S-transferase (GST) activities with rejuvenation of hepatic and pancreatic micro-anatomical features. These outcomes disclosed that AFS is endowed with biologically effective components which could be decent applicant to attain the objective of glycation, oxidative stress and mitigating diabetes-related complications.
  • ||||||||||  Journal, Metastases:  Inhibition of Advanced Glycation End Products (AGEs) by Fermented Foods Using Lactic Acid Bacteria. (Pubmed Central) -  Sep 1, 2024   
    Therefore, it is necessary to identify starter strains of LAB to produce fermented food to decrease the risk of DM and its complications. This chapter introduces the protocols that are inhibition assay of fermented food using LAB on AGEs such as N?-(carboxymethyl) arginine (CMA), N?-(carboxymethyl) lysine (CML), and fluorescent AGEs.
  • ||||||||||  The glycation-lowering formulation Gly-Low improves Alzheimer (MCP Hall A) -  Aug 22, 2024 - Abstract #Neuroscience2024Neuroscience_2636;    
    These data demonstrate that APOE genotype influences the impact of the beneficial effects of Gly-Low. The well-known importance of age and the progeroid effect of APOE4 on AD highlight the potential to use geroscience approaches in the prevention and treatment of AD.
  • ||||||||||  Preclinical, Journal, Metastases:  Role of advanced glycation end-products in age-associated kidney dysfunction in naturally aging mice. (Pubmed Central) -  Aug 17, 2024   
    The well-known importance of age and the progeroid effect of APOE4 on AD highlight the potential to use geroscience approaches in the prevention and treatment of AD. These findings underscore the critical role of AGEs in age-related renal dysfunction and highlight the therapeutic potential of aminoguanidine in mitigating fibrosis and senescence, offering prospective avenues for combating age-associated renal ailments.
  • ||||||||||  Journal:  RAGE mediates hippocampal pericyte responses and neurovascular unit lesions after TBI. (Pubmed Central) -  Aug 4, 2024   
    In contrast, mouse behavioural testing and doublecortin staining indicated that targeting the HMGB1-S100B/RAGE axis after CCI could protect neurological function by reducing pericyte-associated BBB damage. In conclusion, the present study provides experimental evidence for the strong correlation between the pericyte HMGB1-S100B/RAGE axis and NVU damage in the hippocampus at the early stage of TBI and further demonstrates that pericyte RAGE serves as an important target for the protection of neurological function after TBI.
  • ||||||||||  SP-1000 / Samaritan Pharma
    COVID-19 SPIKE AND PARTICULATE MATTER CO-EXPOSURE: IN VITRO MODELING OF INFLAMMATION (Convention Center Exhibit Hall: Rapid Fire Area 1D) -  Jul 31, 2024 - Abstract #CHEST2024CHEST_2929;    
    At SP100 and SP1000, the cells may have reached an inflammatory ceiling, with IL-6 at or greater than that of the LPS cells. PM exposure trends towards increasing IL-6 in a dose dependent manner.
  • ||||||||||  azeliragon (TTP488) / Cantex Pharma
    Journal:  Involvement of RAGE in radiation-induced acquisition of malignant phenotypes in human glioblastoma cells. (Pubmed Central) -  Jul 28, 2024   
    Both phenotypes were suppressed by specific inhibitors of RAGE (FPS-ZM1 and TTP488) or by knockdown of RAGE...In addition, ?-irradiation-induced phosphorylation of STAT3 was suppressed by RAGE inhibitors, and a STAT3 inhibitor suppressed ?-irradiation-induced enhancement of cell migration, indicating that STAT3 is involved in the migration enhancement downstream of RAGE. Our results suggest that HMGB1-RAGE-STAT3 signaling is involved in radiation-induced enhancement of GBM cell migration, and may contribute to GBM recurrence by promoting metastasis and invasion.
  • ||||||||||  resatorvid (TAK-242) / Takeda, Akaza Bioscience
    S100A9 and HMGB1 regulate MDSC-mediated immunosuppression in melanoma (ePoster Self-Study 3) -  Jul 11, 2024 - Abstract #ADO2024ADO_37;    
    S100A9 and HMGB1 convert healthy donor-derived monocytes into MDSC mainly through TLR4 signaling. Our results underscore the prognostic value of plasma S100A8/9 and suggest the potential of targeting TLR4 or S100A8/9 as a strategy to inhibit MDSC-mediated immunosuppression in melanoma.
  • ||||||||||  resatorvid (TAK-242) / Takeda, Akaza Bioscience
    S100A8/9 regulates MDSC-mediated immunosuppression and predicts poor response to immune checkpoint inhibitors in melanoma (East Foyer) -  May 31, 2024 - Abstract #CIMT2024CIMT_231;    
    The immunosuppressive capacity of stimulated monocytes was assessed in the functional assays with T cells with or without TLR4 inhibitor (Resatorvid) and RAGE inhibitor (FPS-ZM1)...Blockade of TLR4 and, to a lesser extent, RAGE signaling, attenuated the suppression of T cell proliferation. In conclusion, these results highlight the prognostic importance of S100A8/9 and suggest the potential of targeting TLR4 signaling as a strategy to counteract MDSC-mediated immunosuppression in melanoma.
  • ||||||||||  Herceptin (trastuzumab) / Roche, azeliragon (TTP488) / Cantex Pharma, Perjeta (pertuzumab) / Roche
    RAGE inhibition to decrease cancer therapy related cardiotoxicity in women with early breast cancer (RAGE). (Hall A; Poster Bd #: 207a) -  Apr 24, 2024 - Abstract #ASCO2024ASCO_1347;    
    P1/2
    In Cohort 4, 6 patients will receive dose dense doxorubicin and cyclophosphamide (ddAC)...As of 2/1/24, 4 patients have been enrolled, with 4 undergoing screening. At the completion of this trial, we plan a randomized trial to evaluate the role of TTP488 to decrease cardiotoxicity, cancer related cognitive decline and disease recurrence.
  • ||||||||||  Transcriptomic Heterogeneity of the Distal Epithelium in IPF Lung: Rethinking the Order of Events (San Diego Convention Center, Room 31A-C (Upper Level)) -  Feb 20, 2024 - Abstract #ATS2024ATS_3196;    
    Our study implies that within relatively normal tissue architecture, the distal epithelium in IPF apices is not yet dysregulated. The decline in AGER transcripts in IPF lungs correlated with histological loss of normal architecture and taken together, suggests that epithelial dysfunction occurs after fibrosis has already started.
  • ||||||||||  Review, Journal:  Urine-derived stem cell therapy for diabetes mellitus and its complications: progress and challenges. (Pubmed Central) -  Feb 8, 2024   
    This review outlines the biological properties of USCs and the research progress and current limitations of their role in DM and related complications. In summary, USCs have shown good versatility in treating hyperglycemia-impaired target organs in preclinical models, and many challenges remain in translating USC therapies to the clinic.
  • ||||||||||  Preclinical, Journal:  Differential Modulation of Mouse Intestinal Organoids with Fecal Luminal Factors from Obese, Allergic, Asthmatic Children. (Pubmed Central) -  Jan 27, 2024   
    The intestinal content of asthmatic obese children differentially induced the expression of inflammatory and mitochondrial response genes (Tnf-tumor necrosis factor, Cd14, Muc13-mucin 13, Tff2-Trefoil factor 2 and Tff3, Cldn1-claudin 1 and 5, Reg3g-regenerating family member 3 gamma, mt-Nd1-NADH dehydrogenase 1 and 6, and mt-Cyb-mitochondrial cytochrome b) via the RAGE-advanced glycosylation end product-specific receptor, NF-?B-nuclear factor kappa b and AKT kinase signal transduction pathways. Fecal homogenates from asthmatic normal-weight and obese children induce a differential phenotype in intestinal organoids, in which the presence of obesity plays a major role.