microRNA-181a-5p impedes the proliferation, migration, and invasion of retinoblastoma cells by targeting the NRAS proto-oncogene

Abstract Objectives Accumulating research have reported that microRNAs (miRNAs) play important roles in Retinoblastoma (RB). Nonetheless, the function and underlying mechanism of miR-181a-5p in RB remain ambiguous. Methods The relative expression levels of miR-181a-5p and NRAS mRNA were detected by quantitative Reverse Transcription-Polymerase Chain Reaction (qRT-PCR). RB cell proliferation was measured using the Cell Counting Kit-8 (CCK-8) and 5′-Bromo-2′-deoxyuridine (BrdU) assays. Transwell assays and flow cytometry were performed to detect the migration, invasion, and apoptosis of RB cells. The interaction between miR-181a-5p and NRAS was explored using luciferase experiments, western blotting, and qRT-PCR. Results miR-181a-5p expression was found to be decreased in RB tissues and cell lines, and its expression was correlated with unfavorable pathological features of the patients. In vitro experiments revealed that miR-181a-5p reduced RB cell proliferation, migration, and invasion while enhancing apoptosis. Further research confirmed that NRAS is a direct target of miR-181a-5p. miR-181a-5p inhibited NRAS expression at both the mRNA and protein levels. Co-transfection of pcDNA-NRAS or NRAS small interfering RNA (siRNA) reversed the effects of miR-181a-5p mimics or miR-181a-5p inhibitors on RB cells. Conclusion miR-181a-5p was significantly downregulated during the development of RB, and it suppressed the malignant behaviors of RB cells by targeting NRAS.

Combined treatment of Pseudomonas aeruginosa PA01 biofilm formation with the water-soluble extract of Ligustrum sinense and gentamicin sulphate.

Ligustrum sinense are commonly used for their anti-inflammatory, anti-rheumatic, diuretic, and hypotensive activities in traditional Chinese medicine. To observe the effects of the combined treatment of a water-soluble extract of Ligustrum sinense (WEL) and gentamicin sulphate (GS) on Pseudomonas aeruginosa PA01, the micro-dilution method was used to determine the minimal inhibitory concentration (MIC) of GS. Formation of a PA01 biofilm was observed under an optical microscope after treatment with different dosages of WEL and combined treatment with GS. The MIC of WEL was 8g l-1, and permanent activity was also observed. The effect of WEL with GS was synergistic. The motility, biomass of biofilms, and production of pyocyanin of P. aeruginosa were strongly suppressed in the presence of WEL. The conclusion can be drawn that combined antibiotics can be used to treat the contamination due to the biofilm formation caused by P. aeruginosa.