Author/Authors :
Chen، نويسنده , , Yang and Liu، نويسنده , , Wei and Chao، نويسنده , , Tengfei (Tim) Zhang، نويسنده , , Yu and Yan، نويسنده , , Xingqi and Gong، نويسنده , , Yanhua and Qiang، نويسنده , , Boqin and Yuan، نويسنده , , Jiangang and Sun، نويسنده , , Maosheng and Peng، نويسنده , , Xiaozhong، نويسنده ,
Abstract :
MicroRNAs have been linked to different cancer-related processes. The microRNA miR-21 appears to function as an anti-apoptosis factor in glioblastomas. However, the functional target genes of miR-21 are largely unknown in glioblastomas. In this study, bioinformatics analysis was used to identify miR-21 target sites in various genes. Luciferase activity assay showed that a number of genes involved in apoptosis, PDCD4, MTAP, and SOX5, carry putative miR-21 binding sites. Expression of PDCD4 protein correlates inversely with expression of miR-21 in a number of human glioblastoma cell lines such as T98G, A172, U87, and U251. Inhibition of miR-21 increases endogenous levels of PDCD4 in cell line T98G and over-expression miR-21 inhibits PDCD4-dependent apoptosis. Together, these results indicate that miR-21 expression plays a key role in regulating cellular processes in glioblastomas and may serve as a target for effective therapies.
Keywords :
Glioblastomas , miR-21 , PDCD4 , T98G