Show pageBacklinksCite current pageExport to PDFBack to top This page is read only. You can view the source, but not change it. Ask your administrator if you think this is wrong. A total of 50 pairs of [[glioma]] [[tissue]] samples and para-[[carcinoma]] tissue samples were collected. Human glioma cell line ([[U251]]) and normal human [[astrocyte]] (NHA) were cultured. The expression of [[RNA]] and [[protein]] was detected by quantitative [[real-time polymerase chain reaction]] (qRT-PCR) and [[Western blot]], respectively. [[Cell proliferation]] assay and transwell assay were used to detect the activities of proliferation and invasion. [[Luciferase]] reporter assays were carried out to determine the binding efficiency between forkhead box O1 ([[FOXO1]]) and miR-135a in U251 cells. qRT-PCR results showed that miR-135a expression was significantly reduced while FOXO1 was up-regulated in glioma tissues. miR-135a overexpression in U251 cells could prominently inhibit proliferation and invasion according to the transwell assays. Moreover, FOXO1 was recognized as the target for miR-135a and may partially reverse the functions of miR-135a in U251 cells. Shi et al., from the Yantaishan Hospital, Yantai, China, showed that miR-135a inhibits [[glioma cell]] proliferation and invasion by down-regulating the target gene FOXO1 ((Shi HZ, Wang DN, Xu F, Teng JH, Wang YL. miR-135a inhibits glioma cell proliferation and invasion by directly targeting FOXO1. Eur Rev Med Pharmacol Sci. 2018 Jul;22(13):4215-4223. doi: 10.26355/eurrev_201807_15415. PubMed PMID: 30024610. )). mir_135.txt Last modified: 2024/06/07 02:59by 127.0.0.1