| Literature DB >> 26216549 |
Naoto Fujiwara1, Jun Inoue2, Tatsuyuki Kawano3, Kousuke Tanimoto2, Ken-Ichi Kozaki4, Johji Inazawa5.
Abstract
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 chemotherapy-induced 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. ©2015 American Association for Cancer Research.Entities:
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Year: 2015 PMID: 26216549 DOI: 10.1158/0008-5472.CAN-15-0257
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701