Increasing reports have demonstrated that aberrant expression of microRNAs (miRNAs) is found in multiple human cancers. Many studies have shown that down-regulated level of miR-30a is in a variety of cancers including prostate cancer (PCa). However, the precise mechanisms of miR-30a in PCa have not been well explored. In this study, we investigated the biological functions and molecular mechanism of miR-30a in PCa cell lines, discussing whether it could be a therapeutic biomarker of PCa in the future. We found that miR-30a is down-regulated in PCa tissues and cell lines. Moreover, the low level of miR-30a was associated with increased expression of SIX1 in PCa tissues and cell lines. Up-regulation of miR-30a significantly inhibited proliferation of PCa cells. In addition, invasion of PCa cells was suppressed by overexpression of miR-30a. However, down-regulation of miR-30a promoted cell growth and invasion of PCa cells. Bioinformatics analysis predicted that the SIX1 was a potential target gene of miR-30a. Next, luciferase reporter assay confirmed that miR-30a could directly target SIX1. Consistent with the effect of miR-30a, down-regulation of SIX1 by siRNA inhibited proliferation and invasion of PCa cells. Overexpression of SIX1 in PCa cells partially reversed the effect of miR-30a mimic. In conclusion, introduction of miR-30a dramatically inhibited proliferation and invasion of PCa cells by down-regulating SIX1 expression, and that down-regulation of SIX1 was essential for inhibition of cell growth and invasion of PCa cells by overexpression of miR-30a.
The reproduction and early growth of fish are essential elements that affect recruitment and provide breakthrough points for understanding population fluctuations. In this study, larval and juvenile Japanese anchovy (Engraulis japonicus) were collected from five coastal waters off the Pacific coast of Japan in 2020 and 2021 to gain more insight into life history traits such as reproduction and early growth of this species on the basis of otolith microstructure analysis. The spawning period appeared to be related to temperature and chlorophyll-a concentrations, showing latitudinal gradient variation among fishing areas. We detected a significant positive allometric growth pattern between standard length and body weight. The Gompertz model best fits the growth of standard length, showing an initial stage of growth that was quick and accelerating. The mean daily growth rate for standard length was 0.64 ± 0.09 mm per day. A series of mixed-effect models was constructed to investigate the sources of differences in the mean growth rates among individuals. The results revealed regional variability in fish growth, with individuals in the central Pacific stock growing faster. Individuals that grew slower were heavier than those of the same length, indicating a trade-off between length growth and weight growth. The mean growth of individual fish was positively influenced by environmental factors (surface water temperature and chlorophyll-a concentration), and individuals within the same school of fish displayed a striking homogeneity of growth. Our research demonstrates the significance of including both physiological characteristics and environmental influences in early growth studies on fish.
Background:
To systematically evaluate the clinical risk factors of patients with systemic lupus erythematosus (SLE) complicated with invasive fungal infection (IFI) among patients.
Methods:
A meta-analysis was performed of all the literatures germane to estimate the clinical risk factors of patients with SLE complicated with IFI from published clinical trials from 1990 to April 2022. Mean differences, odds ratio and 95% confidence intervals were calculated, and the meta-analysis was conducted with Stata 12.0 software (StataCorp, College Station, TX).
Results:
A total of 14 clinical research involving 1129 patients were included. The results of meta-analysis demonstrated that immunosuppressant, glucocorticoids, systemic lupus erythematosus disease activity index score, antibiotic were risk factors associated with IFI in SLE patients. However, age, sex, course of disease, leukopenia, lymphopenia, C- reactive protein and hypoproteinemia were not the risk factors associated with IFI in patients with SLE.
Conclusion:
Our results indicate that immunosuppressant, glucocorticoids, systemic lupus erythematosus disease activity index score, antibiotic were risk factors for IFI in SLE patients. However, high quality of multicenter, large sample size-controlled trials are needed to validate the result.
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