The tumor-suppressive and potential therapeutic functions of miR-34a in epithelial carcinomas

被引:128
作者
Adams, Brian D. [1 ,2 ]
Parsons, Christine [1 ]
Slack, Frank J. [2 ]
机构
[1] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT USA
[2] Harvard Univ, Sch Med, Dept Pathol, BIDMC Canc Ctr, 3 Blackfan Circle, Boston, MA 02215 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
Biomarker; breast cancer; cancer; lung; microRNA; miR-34; therapy; treatment resistance; tumor suppressor; BREAST-CANCER CELLS; COLON-CANCER; LUNG-CANCER; DOWN-REGULATION; C-MET; MOTILE CILIOGENESIS; INHIBITS MIGRATION; SYSTEMIC DELIVERY; FEEDBACK LOOP; CLL PATIENTS;
D O I
10.1517/14728222.2016.1114102
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Introduction: Many RNA species have been identified as important players in the development of chronic diseases including cancer. Certain classes of regulatory RNAs such as microRNAs (miRNAs) have been investigated in such detail that bona fide tumor suppressive and oncogenic miRNAs have been identified. Because of this, there has been a major effort to therapeutically target these small RNAs. One in particular, a liposomal formulation of miR-34a (MRX34), has entered Phase I trials. Areas covered: This review aims to summarize miRNA biology, its regulation within normal versus disease states and how it can be targeted therapeutically, with a particular emphasis on miR-34a. Understanding the complexity of a single miRNA will aid in the development of future RNA-based therapeutics for a broader range of chronic diseases. Expert opinion: The potential of miRNAs to be developed into anti-cancer therapeutics has become an increasingly important area of research. miR-34a is a tumor suppressive miRNA across many tumor types through its ability to inhibit cellular proliferation, invasion and tumor sphere formation. miR-34a also shows promise within certain in vivo solid tumor models. Finally, as miR-34a moves into clinical trials it will be important to determine if it can further sensitize tumors to certain chemotherapeutic agents.
引用
收藏
页码:737 / 753
页数:17
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