pylori. Activation of the RAGE/multiligand axis is thought to be a relevant factor in cancer-mediated inflammation. RAGE is a membrane receptor, belonging to the immunoglobulin family, and the over-expression of RAGE has been associated with increased invasiveness and metastasis generation in different types of cancer, including gastric cancer. Furthermore recent experiences show that the use of its soluble form (sRAGE) or silencing of the gene coding for this receptor could provide therapeutic benefits in cancer. Aim: To evaluate the immunohistochemical expression of RAGE, MUC-1, beta-Catenin free and phosphorylated, Cyclin-D 1 and GSK3 in gastric biopsy specimens infected
AG-881 cell line with H. pylori. Material and Methods: Immunohistochemical analysis was carried out in gastric biopsies from 138 patients: 55 with inflammatory injury (no atrophic gastritis), 42 with pre-cancerous conditions. (atrophy or intestinal metaplasia) and 41 with dysplastic
lesions or in situ adenocarcinoma. Results: There was a high rate of positive RAGE expression PD-1/PD-L1 inhibitor in the three groups of biopsies. Biopsies with dysplasia or in situ carcinoma had a significantly higher percentage of RAGE expression than the other groups of biopsies. Conclusions: The increased RAGE expression reported in both dysplasia and incipient cancer support the role of the multiligand/RAGE axis in gastric carcinogenesis.”
“Background: Vitamin D receptor(VDR), Th17 related CC chemokine receptor 6(CCR6), Treg related Foxp3 and CD8+T related granzyme B(GrB) contributed to the development of many autoimmune diseases. However, there are no available data addressing the expression of these mRNA of these proteins in the muscles in idiopathic inflammatory
myopathy (IIM) and limb-girdle muscular dystrophy type 2B (LGMD2B). Methods: We have evaluated the levels of 4 mRNAs including VDR, CCR6, Foxp3, GrB in the muscle and muscle related enzymes in the blood of 14 patients with idiopathic inflammatory myopathy, 4 patients with LGMD2B and 7 controls who did not have histopathological signs of any muscle diseases. Results: The expressions of all measured mRNAs and muscle related enzymes were highest in IIM. The mRNA levels in LGMD2B were also higher than those in the controls. A significant difference of VDR mRNA expression was observed between IIM U0126 solubility dmso and LGMD2B. Conclusions: Th17, Treg, CD8+T are involved in the development of IIM and LGMD2B. The elevation of VDR expression may provide us with clues as a potential therapy to treat these diseases.”
“Propranolol, as a non-selective blocker of the beta-adrenergic receptor (AR), is utilised as the first-line treatment for infantile hemangiomas. However, the underlying mechanism remains poorly understood. The present study was designed to investigate the molecular basis of propranolol on the regression of infantile hemangiomas using a proliferating infantile hemangioma-derived endothelial cell line.