Developing therapeutic microRNAs for cancer

被引:267
作者
Bader, A. G. [1 ]
Brown, D. [1 ]
Stoudemire, J. [1 ]
Lammers, P. [1 ]
机构
[1] Mirna Therapeut Inc, R&D, Austin, TX 78744 USA
关键词
microRNA; miRNA replacement therapy; oncomir; let-7; miR-34a; IN-VIVO; BREAST-CANCER; LUNG-CANCER; RNA; METASTASIS; DELIVERY; SIRNA; CELLS; MODEL; INHIBITION;
D O I
10.1038/gt.2011.79
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
Despite substantial progress in understanding the cancer-signaling network, effective therapies remain scarce due to insufficient disruption of oncogenic pathways, drug resistance and drug-induced toxicity. This complexity of cancer defines an urgent goal for researchers and clinicians to develop novel therapeutic strategies. The discovery of microRNAs (miRNAs) provides new hope for accomplishing this task. Supported by solid evidence for a critical role in cancer and bolstered by a unique mechanism of action, miRNAs are likely to yield a new class of targeted therapeutics. In contrast to current cancer medicines, miRNA-based therapies function by subtle repression of gene expression on a yet large number of oncogenic factors and are, therefore, anticipated to be highly efficacious. After the completion of target validation for several candidates, the development of therapeutic miRNAs is now moving to a new stage that involves pharmacological drug delivery, preclinical toxicology and regulatory guidelines. Gene Therapy (2011) 18, 1121-1126; doi:10.1038/gt.2011.79; published online 2 June 2011
引用
收藏
页码:1121 / 1126
页数:6
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