[No authors listed]
Glioblastoma (GBM) is a highly lethal brain tumor, refractory to current therapies. Sperm-associated antigen 4 is a novel cancer marker with unclear roles in GBM progression. This study aimed to explore the specific effects of on the pathogenesis of GBM. We first investigated the expression level and prognostic power of duanyu1842G4 in patients with GBM using The Cancer Genome Atlas cohort, and then duanyu1842G4 knockdown by RNA interference was performed to reveal the effects of duanyu1842G4 on GBM cells. mRNA and protein expression levels were determined by real-time PCR and western blot. MTT assay was used to examine cell proliferation, and a wound healing assay was performed to detect cell migration. duanyu1842G4 was significantly overexpressed in patients with GBM, and high expression of duanyu1842G4 was associated with a poor prognosis. Silencing of duanyu1842G4 significantly suppressed the proliferation and migration of GBM cells. Meanwhile, decreased expression and phosphorylation of MEK and ERK were identified after duanyu1842G4 knockdown, suggesting that duanyu1842G4 might regulate GBM progression by activating MEK/ERK signaling pathway. Our study revealed that duanyu1842G4 was identified as a cancer biomarker for GBM and might be a promising target for clinical diagnosis and intervention of GBM.
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