Upregulated AHIF-mediated radioresistance in glioblastoma

被引:13
|
作者
Liao, Keman [1 ]
Ma, Xiumei [2 ]
Chen, Binghong [1 ]
Lu, Xiaojie [4 ]
Hu, Yaomin [5 ]
Lin, Yingying [1 ]
Huang, Renhua [2 ,3 ]
Qiu, Yongming [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Renji Hosp, Dept Neurosurg, Room 118,Bldg 11,1630 Dongfang Rd, Shanghai, Peoples R China
[2] Shanghai Jiao Tong Univ, Renji Hosp, Sch Med, Dept Radiat, First Floor,Bldg 3,1630 Dongfang Rd, Shanghai, Peoples R China
[3] Soochow Univ, Affiliated Hosp 2, Dept Nucl Accid Med Emergency, Suzhou, Peoples R China
[4] Nanjing Med Univ, Wuxi Hosp 2, Dept Neurosurg, Wuxi, Peoples R China
[5] Shanghai Jiao Tong Univ, Sch Med, Renji Hosp, Dept Endocrinol, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
Glioblastoma; AHIF; Radiotherapy; Apoptosis; POTENTIAL ROLE; ANTISENSE; GLIOMA; TRANSCRIPT; CELLS;
D O I
10.1016/j.bbrc.2018.12.136
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
Long non-coding RNAs (lncRNAs) play vital roles in the pathobiology of glioblastoma multiforme (GBM). Though radiotherapy remains the most effective component of multiple therapies for patients with GBM, lncRNAs conferring GBM radioresistance are less unknown. Here, the present study identified that the antisense transcript of hypoxia-inducible factor-1 alpha (AHIF) was upregulated in GBM cells after radiotherapy. The deregulation of AHIF affected GBM cell clonogenic formation, DNA repair and apoptosis. Notably, knockdown of AHIF inhibited tumorigenesis after radiotherapy in vivo. Further biochemical analysis identified that AHIF regulated proteins associated with apoptosis after radiotherapy. Thus, the present data illustrate that suppression of AHIF increases radiosensitivity in GBM cells, which may be a potential diagnostic and therapeutic target for GBM patients. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:617 / 623
页数:7
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