Key result
Atorvastatin inhibited proliferation, invasion, and migration and promoted apoptosis of human glioma cells, possibly by up-regulating miR-146a and inhibiting the PI3K/Akt signaling pathway.
Why the study?
Does atorvastatin inhibit malignant behaviors and induce apoptosis in human glioma cells?
Does atorvastatin inhibit malignant behaviors and induce apoptosis in human glioma cells?
Atorvastatin demonstrates anti-tumor effects in human glioma cells in vitro by modulating the miR-146a/PI3K/Akt signaling pathway.
Answers are grounded in this paper and cite their sources.
Hypothesis-generating in glioma cell lines; leaves open whether atorvastatin effects translate to clinical benefit.
OBJECTIVE: To explore the effect of atorvastatin (AVT) on biological behaviors and the miR-146a/PI3K/Akt signaling pathway in human glioma cells. METHODS: Human glioma U251 cells were treated with 8.0 μmol/L AVT or transfected with a miR-146a inhibitor or a negative control fragment (miR-146a NC) prior to AVT treatment. RT-PCR was used to detect miR-146a expression in the cells, and the changes in cell proliferation rate, apoptosis, cell invasion and migration were detected using MTT assay, flow cytometry, and Transwell assay. Western blotting was performed to detect the changes in cellular expressions of proteins in the PI3K/Akt signaling pathway. CONCLUSION: AVT can inhibit the proliferation, invasion and migration and promote apoptosis of human glioma cells possibly by up-regulating miR-146a expression and inhibiting the PI3K/Akt signaling pathway.
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Cui et al. (2022) studied Human glioma. Atorvastatin vs. miR-146a inhibitor or negative control was evaluated on Cell proliferation rate, apoptosis, cell invasion and migration (p=>0.05). Atorvastatin inhibited proliferation, invasion, and migration and promoted apoptosis of human glioma cells, possibly by up-regulating miR-146a and inhibiting the PI3K/Akt signaling pathway.
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