Journal
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Volume 111, Issue 34, Pages E3553-E3561Publisher
NATL ACAD SCIENCES
DOI: 10.1073/pnas.1412686111
Keywords
miR-34; nanotechnology
Categories
Funding
- National Institutes of Health [2-PO1-CA42063, RO1-EB000244, RO1-CA115527, RO1-CA132091]
- National Cancer Institute [P30-CA14051]
- Leukemia Lymphoma Society
- National Defense Science and Engineering Graduate
- National Science Foundation Graduate Research Fellowship Program
- Massachusetts Institute of Technology Presidential Fellowships
- American Association for Cancer Research
- [1K99CA169512]
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MicroRNAs (miRNAs) and siRNAs have enormous potential as cancer therapeutics, but their effective delivery to most solid tumors has been difficult. Here, we show that a new lung-targeting nanoparticle is capable of delivering miRNA mimics and siRNAs to lung adenocarcinoma cells in vitro and to tumors in a genetically engineered mouse model of lung cancer based on activation of oncogenic Kirsten rat sarcoma viral oncogene homolog (Kras) and loss of p53 function. Therapeutic delivery of miR-34a, a p53-regulated tumor suppressor miRNA, restored miR-34a levels in lung tumors, specifically down-regulated miR-34a target genes, and slowed tumor growth. The delivery of siRNAs targeting Kras reduced Kras gene expression and MAPK signaling, increased apoptosis, and inhibited tumor growth. The combination of miR-34a and siRNA targeting Kras improved therapeutic responses over those observed with either small RNA alone, leading to tumor regression. Furthermore, nanoparticle-mediated small RNA delivery plus conventional, cisplatin-based chemotherapy prolonged survival in this model compared with chemotherapy alone. These findings demonstrate that RNA combination therapy is possible in an autochthonous model of lung cancer and provide preclinical support for the use of small RNA therapies in patients who have cancer.
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