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In Vivo Selection Against Human Colorectal Cancer Xenografts Identifies an Aptamer That Targets RNA Helicase Protein DHX9

Authors :
David S. Hsu
Jennifer Xu
Chien-Tsun Kuan
Bryan M. Clary
Bruce A. Sullenger
Partha Ray
Jenny Liu
Jing Mi
Rebekah R. White
Source :
Molecular Therapy. Nucleic Acids, Mi, J; Ray, P; Liu, J; Kuan, C-T; Xu, J; Hsu, D; et al.(2016). In Vivo Selection Against Human Colorectal Cancer Xenografts Identifies an Aptamer That Targets RNA Helicase Protein DHX9. MOLECULAR THERAPY-NUCLEIC ACIDS, 5. doi: 10.1038/mtna.2016.27. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/4769d4pn, Molecular therapy. Nucleic acids, vol 5, iss 4, Molecular Therapy: Nucleic Acids, Vol 5, Iss C (2016)
Publication Year :
2016
Publisher :
Elsevier BV, 2016.

Abstract

The ability to selectively target disease-related tissues with molecules is critical to the design of effective therapeutic and diagnostic reagents. Recognizing the differences between the in vivo environment and in vitro conditions, we employed an in vivo selection strategy to identify RNA aptamers (targeting motifs) that could localize to tumor in situ. One of the selected molecules is an aptamer that binds to the protein DHX9, an RNA helicase that is known to be upregulated in colorectal cancer. Upon systemic administration, the aptamer preferentially localized to the nucleus of cancer cells in vivo and thus has the potential to be used for targeted delivery.

Details

ISSN :
21622531
Volume :
5
Database :
OpenAIRE
Journal :
Molecular Therapy - Nucleic Acids
Accession number :
edsair.doi.dedup.....8ca21a6a21a150fd5e9736f21e88e2f6
Full Text :
https://doi.org/10.1038/mtna.2016.27