miR-634 Activates the Mitochondrial Apoptosis Pathway and Enhances Chemotherapy-Induced Cytotoxicity

被引:64
作者
Fujiwara, Naoto [1 ,2 ,3 ]
Inoue, Jun [1 ,2 ]
Kawano, Tatsuyuki [3 ]
Tanimoto, Kousuke [1 ,2 ]
Kozaki, Ken-ichi [4 ]
Inazawa, Johji [1 ,2 ,5 ,6 ]
机构
[1] Tokyo Med & Dent Univ, Med Res Inst, Dept Mol Cytogenet, Tokyo 1138510, Japan
[2] Tokyo Med & Dent Univ, Grad Sch Med & Dent Sci, Tokyo 1138510, Japan
[3] Tokyo Med & Dent Univ, Dept Esophageal & Gen Surg, Grad Sch, Tokyo 1138510, Japan
[4] Okayama Univ, Dept Dent Pharmacol, Grad Sch, Okayama 7008530, Japan
[5] Tokyo Med & Dent Univ, Dept Genome Med, Hard Tissue Genome Res Ctr, Tokyo 1138510, Japan
[6] Tokyo Med & Dent Univ, Bioresource Res Ctr, Tokyo 1138510, Japan
基金
日本学术振兴会;
关键词
CARCINOMA-CELLS; DNA HYPERMETHYLATION; THERAPEUTIC TARGET; DOWN-REGULATION; REGULATES XIAP; IN-VITRO; CANCER; MICRORNA; RESISTANCE; AUTOPHAGY;
D O I
10.1158/0008-5472.CAN-15-0257
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Some tumor-suppressing miRNAs target multiple oncogenes concurrently and therefore may be useful as cancer therapeutic agents. Further, such miRNAs may be useful to address chemotherapeutic resistance in cancer, which remains a primary clinical challenge in need of solutions. Thus, cytoprotective processes upregulated in cancer cells that are resistant to chemotherapy are a logical target for investigation. Here, we report that overexpression of miR-634 activates the mitochondrial apoptotic pathway by direct concurrent targeting of genes associated with mitochondrial homeostasis, antiapoptosis, antioxidant ability, and autophagy. In particular, we show how enforced expression of miR-634 enhanced chemotherapyinduced cytotoxicity in a model of esophageal squamous cell carcinoma, where resistance to chemotherapy remains clinically problematic. Our findings illustrate how reversing miR-634-mediated cytoprotective processes may offer a broadly useful approach to improving cancer therapy. (C) 2015 AACR.
引用
收藏
页码:3890 / 3901
页数:12
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