FOXO4 expression associates with glioblastoma development and FOXO4 expression inhibits cell malignant phenotypes in vitro and in vivo

FOXO4 表达与胶质母细胞瘤发展相关,且 FOXO4 表达在体内和体外抑制细胞恶性表型

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作者:Min Qi, Le-An Sun, Xiao-Chun Jiang, Yan-Ling Han, Lin Wang, Wen-Hao Niu, Mao-Xing Fei, Wang-Dui Zhaba, Lan-Rong Zheng, Meng-Liang Zhou

Aim

Forkhead box protein O4 (FOXO4) is a transcription factor, and aberrant FOXO4 expression is associated with development of various human cancers. This study explored the role of FOXO4 in glioma in vitro and in vivo.

Methods

FOXO4 expression was first assessed in normal brain tissues, low-grade glioma, glioblastoma multiforme (GBM), normal human astrocytes (HA), and GBM cell lines, while manipulation of FOXO4 expression in glioma cell lines was assessed using qRT-PCR, Western blot, and cell viability CCK-8, Transwell, and a nude mouse subcutaneous xenograft assays. Key findings: The data showed downregulated FOXO4 expression in GBM tissues and cell lines. FOXO4 overexpression induced by transfection with FOXO4 cDNA significantly inhibited GBM cell proliferation, migration, and invasion, but increased tumor cells to undergo apoptosis in vitro, while suppressed growth of GBM cell subcutaneous xenografts in nude mice. In

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