GCN5 Potentiates Glioma Proliferation and Invasion via STAT3 and AKT Signaling Pathways

被引:38
|
作者
Liu, Kun [1 ,2 ]
Zhang, Qing [1 ,2 ]
Lan, Haitao [3 ,4 ]
Wang, Liping [2 ]
Mou, Pengfei [1 ,2 ]
Shao, Wei [1 ,2 ]
Liu, Dan [1 ,2 ]
Yang, Wensheng [1 ,2 ]
Lin, Zhen [1 ,2 ]
Lin, Qingyuan [1 ,2 ]
Ji, Tianhai [1 ,2 ]
机构
[1] Xiamen Univ, Affiliated Chenggong Hosp, Dept Pathol, Xiamen 361000, Peoples R China
[2] Anhui Med Univ, Chinese Peoples Liberat Army, Clin Coll 174, Xiamen 361000, Peoples R China
[3] Sichuan Acad Med Sci, Dept Oncol, Chengdu 610072, Peoples R China
[4] Sichuan Prov Peoples Hosp, Chengdu 610072, Peoples R China
基金
中国国家自然科学基金;
关键词
GCN5; cell proliferation; cell invasion; STAT3; MALIGNANT GLIOMA; ACETYLATION; CANCER; EXPRESSION; PROTEINS; TARGETS;
D O I
10.3390/ijms160921897
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
The general control of nucleotide synthesis 5 (GCN5), which is one kind of lysine acetyltransferases, regulates a number of cellular processes, such as cell proliferation, differentiation, cell cycle and DNA damage repair. However, its biological role in human glioma development remains elusive. In the present study, we firstly reported that GCN5 was frequently overexpressed in human glioma tissues and GCN5 was positively correlated with proliferation of cell nuclear antigen PCNA and matrix metallopeptidase MMP9. Meanwhile, down-regulation of GCN5 by siRNA interfering inhibited glioma cell proliferation and invasion. In addition, GCN5 knockdown reduced expression of p-STAT3, p-AKT, PCNA and MMP9 and increased the expression of p21 in glioma cells. In conclusion, GCN5 exhibited critical roles in glioma development by regulating cell proliferation and invasion, which suggested that GCN5 might be a potential molecular target for glioma treatment.
引用
收藏
页码:21897 / 21910
页数:14
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