Genetically engineered oncolytic adenovirus induces autophagic cell death through an E2F1-microRNA-7-epidermal growth factor receptor axis

被引:53
|
作者
Tazawa, Hiroshi [2 ]
Yano, Shuya
Yoshida, Ryosuke
Yamasaki, Yasumoto
Sasaki, Tsuyoshi [3 ]
Hashimoto, Yuuri
Kuroda, Shinji
Ouchi, Masaaki [4 ]
Onishi, Teppei
Uno, Futoshi
Kagawa, Shunsuke
Urata, Yasuo [4 ]
Fujiwara, Toshiyoshi [1 ]
机构
[1] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Surg Gastroenterol, Kita Ku, Okayama 7008558, Japan
[2] Okayama Univ Hosp, Ctr Gene & Cell Therapy, Okayama, Japan
[3] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Orthopaed Surg, Okayama 7008558, Japan
[4] Oncolys BioPharma Inc, Tokyo, Japan
基金
日本科学技术振兴机构;
关键词
adenovirus; telomerase; microRNA; autophagy; EGFR; CANCER-CELLS; GENE-PRODUCT; MICRORNA; REPLICATION; E2F; APOPTOSIS; PROLIFERATION; TRANSCRIPTION; CONTRIBUTES; EXPRESSION;
D O I
10.1002/ijc.27589
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Autophagy is known to have a cytoprotective role under various cellular stresses; however, it also results in robust cell death as an important safeguard mechanism that protects the organism against invading pathogens and unwanted cancer cells. Autophagy is regulated by cell signalling including microRNA (miRNA), a post-transcriptional regulator of gene expression. Here, we show that genetically engineered telomerase-specific oncolytic adenovirus induced miR-7 expression, which is significantly associated with its cytopathic activity in human cancer cells. Virus-mediated miR-7 upregulation depended on enhanced expression of the E2F1 protein. Ectopic expression of miR-7 suppressed cell viability and induced autophagy by inhibiting epidermal growth factor receptor (EGFR) expression. Our results suggest that oncolytic adenovirus induces autophagic cell death through an E2F1-miR-7-EGFR pathway in human cancer cells, providing a novel insight into the molecular mechanism of an anticancer virotherapy.
引用
收藏
页码:2939 / 2950
页数:12
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