pylori infection. In addition, rebamipide scavenges free radicals, inhibits inflammatory cell responses, and reduces interleukin-8 production in response to H. pylori.[24-26] These effects might alter H. pylori status. The present systematic review https://www.selleckchem.com/products/chir-99021-ct99021-hcl.html and meta-analysis has several limitations

that need to be taken into account in interpreting the results. The most of these studies were performed in Japan, and similar publications examining other ethnic populations are limited. In addition, although most studies in the present analysis evaluated the supplementary effect of rebamipide on the PPI+amoxicillin dual therapy, it is rather outdated because the main stream of the recent H. pylori eradication regimens are based on the triple therapy. Due to the limited number of eligible studies, subgroup analysis was not performed. The highest quality study by Fujioka et al. showed no significant effect of rebamipide (odds ratio 0.86).[22] Further studies with large number of patients are warranted to clarify the efficacy of rebamipide-containing quadruple therapy. In conclusion, our analysis demonstrates that supplementation with rebamipide might be effective in increasing H. pylori eradication rates of PPI–amoxicillin dual therapy.

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“Hepatitis B virus X (HBx) protein is implicated in hepatitis B virus (HBV)-associated liver carcinogenesis. However, it remains unclear whether HBx-expressing hepatic progenitor cells

(HPCs) are attributed to liver tumor formation. In this study, by using HBx ABT-737 manufacturer transgenic mice and a 3,5-diethoxycarbonyl-1,4-dihydrocollidine Non-specific serine/threonine protein kinase (DDC)-induced liver injury model, the relationship between HBx expression and tumorigenicity of HPCs was analyzed. Compared with control mice, an elevated number of EpCAM+ cells with characteristics of HPCs was observed in HBx mice after 1 month and 4 months of DDC diet feeding. All HBx transgenic mice developed liver tumors characterized by histological features of both hepatocellular carcinoma (HCC) and cholangiocarcinoma after 7 months of DDC feeding. Notably, EpCAM+ HPCs isolated from premalignant HBx mice exposed to a DDC diet for 4 months formed subcutaneous mixed-lineage tumors (four out of six) in nonobese diabetic/severe-combined immunodeficient (NOD/SCID) mice, and none of the cells from wildtype (WT) induced tumor, indicating that HBx may induce malignant transformation of HPCs that contributes to tumorigenesis. We also found higher titers of circulating interleukin (IL)-6, activities of IL-6/STAT3, and Wnt/β-catenin signaling pathways in HBx transgenic mice, suggesting HBx may induce intrinsic changes in HPCs by way of the above signaling that enables HPCs with tumorigenicity potential. Finally, clinical evidence showed that high HBx expression in human HBV-related HCC was statistically associated with expansion of EpCAM+ or OV6+ tumor cells and aggressive clinicopathologic features.