EN1 Regulates Cell Growth and Proliferation in Human Glioma Cells via Hedgehog Signaling

被引:15
作者
Chang, Jinchun [1 ,2 ]
Guo, Chenjia [3 ]
Li, Jianyu [3 ]
Liang, Zhangqian [3 ]
Wang, Yankai [2 ]
Yu, Anliang [2 ]
Liu, Runze [2 ]
Guo, Yuting [2 ]
Chen, Jian [3 ,4 ,5 ]
Huang, Song [2 ]
机构
[1] Beijing Normal Univ, Coll Life Sci, Beijing 100875, Peoples R China
[2] Natl Inst Biol Sci, Beijing 102206, Peoples R China
[3] Chinese Inst Brain Res, Beijing 102206, Peoples R China
[4] Soochow Univ, Inst Funct Nano & Soft Mat FUNSOM, Suzhou 215123, Peoples R China
[5] Soochow Univ, Collaborat Innovat Ctr Suzhou Nano Sci & Technol, Suzhou 215123, Peoples R China
关键词
glioblastoma; Engrailed; irradiation sensitivity; ROS; Hedgehog; TRANSCRIPTION FACTOR; PATHWAY; CANCER; RESISTANCE; BIOMARKER; PROTEINS; ASSAY;
D O I
10.3390/ijms23031123
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Glioblastoma is an aggressive cancer of the nervous system that accounts for the majority of brain cancer-related deaths. Through cross-species transcriptome studies, we found that Engrailed 1 (EN1) is highly expressed in serum-free cultured glioma cells as well as glioma tissues, and increased expression level predicts a worse prognosis. EN1 controls glioma cell proliferation, colony formation, migration, and tumorigenic capacity in vivo. It also influences sensitivity of glioma cells to gamma-ray irradiation by regulating intracellular ROS levels. Mechanistically, EN1 influences Hedgehog signaling by regulating the level of Gli1 as well as primary cilia length and the primary cilia transport-related protein TULP3. In conclusion, we demonstrate that EN1 acts as an oncogenic regulator that contributes to glioblastoma pathogenesis and could serve as a diagnostic/prognostic marker and therapeutic target for glioblastoma.
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收藏
页数:14
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