Abstract. The purpose of this study was to evaluate the bonding ability of four representative dentin-adhesive systems by applying the micro-shear bond strength (μ-SBS) test method and to evaluate the influence of adhesive area limitation on the bond strength. Two different adhesive application methods were used in the μ-SBS test (with and without adhesives area limitation), and four representative adhesive systems were used in this study. Each dentin surface was treated with one of the four representative adhesive systems, and with twenty samples per group (n=20), each of the four groups underwent a μ-SBS test. The results showed that the bond strength was significantly influenced by the adhesive application method (p<0.05), the adhesive type (p<0.05) and the interaction between the two factors (p<0.05). With regard to the four representative dentinadhesive systems, 3-E&R has a much better bond quality compared to the other adhesive systems. Furthermore, the microshear bond strength test method of restricting the area of both the adhesive and the resin is more reliable for evaluating the bonding property of adhesives to dentin, and it is also adequate for comparing the different adhesives systems.
Clusterin (CLU) is a chaperone-like protein that has been demonstrated to have a direct relationship with cancer occurrence, progression, or metastasis. Clusterin was downregulated in tumor tissues using three datasets of tongue squamous carcinoma from the Gene Expression Omnibus. We further retrieved datasets from The Cancer Genome Atlas and Gene Expression Omnibus to thoroughly investigate the carcinogenic consequences of Clusterin. Our findings revealed that decreased Clusterin expression in malignancies was associated with a worse overall survival prognosis in individuals with multiple tumors; Clusterin gene deep deletions were found in almost all malignancies and were connected to most cancer patient’s prognosis, Clusterin DNA methylation level was dependent on tumor type, Clusterin expression was also linked to the invasion of cancer-associated CD8+ T-cells and fibroblasts in numerous cancer forms. Moreover, pathway enrichment analysis revealed that Clusterin primarily regulates biological processes such as cholesterol metabolism, phospholipid binding, and protein-lipid complex formation. Overall, our pan-cancer research suggests that Clusterin expression levels are linked to tumor carcinogenesis and prognosis, which contributes to understanding the probable mechanism of Clusterin in tumorigenesis as well as its clinical prognostic significance.
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