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Fibrosis is a common pathological state characterized by the excessive accumulation of extracellular matrix components, but the pathogenesis of the disease is still not clear. Previous studies have shown that microRNA-29 (miR-29) can play pivotal roles in the regulation of a variety of organ fibrosis, including cardiac fibrosis, hepatic fibrosis, lung fibrosis, systemic sclerosis, and keloid. In this review, we outline the structure, expression, and regulation of miR-29 as well as its role in fibrotic diseases. [ABSTRACT FROM AUTHOR]

Melanoma is a common skin cancer associated with ultraviolet light exposure and genetic variance. However, the etiology and molecular mechanisms of melanoma remain unknown. Recent studies have shown that microRNAs (miRNAs) can play key roles in the development and prognosis of this disease. In this study, we reviewed several pivotal miRNAs that may contribute to melanoma by involvement in the processes of invasion, migration, and metastasis of melanoma cells. [ABSTRACT FROM AUTHOR]

Background and Objective: MicroRNA (miR)-499 rs3746444 polymorphisms may participate in the pathogenesis of autoimmune diseases, but the results remain conflicting. We further investigated this association using a meta-analysis. Methods: We conducted a retrieval of studies and obtained the eligible studies if they met inclusion criteria. Two researchers independently extracted the data from original articles. The genotype frequencies were analysed using Stata software. Results: We finally archived six eligible studies that included 1,118 cases and 1,673 controls. After pooling the data, the results indicated that homozygote TT had an overall association with autoimmune diseases (TC + CC vs. TT: odds ratio [OR] 1.31, 95 % CI 1.11-1.55, p = 0.001). The allele C, genotype TC and CC, may be associated with rheumatoid arthritis (RA) risks in Mediterranean populations (C vs. T: OR 2. 00, 95 % CI 1.37-2.91, p < 0.001; TC vs. CC + TT: OR 1.76, 95 % CI 1.27-2.44; p = 0.001; CC vs. TC + TT: OR 2.31, 95 % CI 1.24-4.27, p = 0.008; CC vs. TT: OR 2.92, 95 % CI 1.59-5.37 , p = 0.001; TC vs. TT: OR 1.98, 95 % CI 1.42-2.77). The genotype TT may decrease the risk of RA in Mediterranean populations (TC + CC vs. TT: OR 2.15, 95 % CI 1.57-2.94, p < 0.001) rather than in East Asians. Conclusions: This study suggested that miR-499 polymorphisms were associated with a significantly increased risk of RA in Mediterranean populations. [ABSTRACT FROM AUTHOR]