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Inhibition of discoidin domain receptor 2-mediated lung cancer cells progression by gold nanoparticle-aptamer-assisted delivery of peptides containing transmembrane-juxtamembrane 1/2 domain

Authors
Kim, DaehwanYeom, Ji-HyunLee, BoeunLee, KangseokBae, JeehyeonRhee, Sangmyung
Issue Date
Aug-2015
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Keywords
Discoidin domain receptor 2; Juxtamembrane domain; DNA aptamer; Gold nanoparticle; Peptide delivery
Citation
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.464, no.2, pp 392 - 395
Pages
4
Journal Title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
Volume
464
Number
2
Start Page
392
End Page
395
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/9220
DOI
10.1016/j.bbrc.2015.06.044
ISSN
0006-291X
1090-2104
Abstract
The delivery of biologically functional peptides into mammalian cells can be a direct and effective method for cancer therapy and treatment of other diseases. Discoidin domain receptor 2 (DDR2) is a collagen-induced receptor tyrosine kinase recently identified as a novel therapeutic target in lung cancer. In this study, we report that peptides containing the functional domain of DDR2 can be efficiently delivered into lung malignant cancer cells via a gold nanoparticle-DNA aptamer conjugate (AuNP-Apt)-based system. Peptide delivery resulted in the abrogation of DDR2 activation triggered by collagen. Moreover, the peptide delivered by the AuNP-Apt system inhibited cancer cell proliferation and invasion mediated by DDR2 activation. Thus, these results suggest that peptide loaded onto AuNP-Apt conjugates can be used for the development of peptide-based biomedical applications for the treatment of DDR2-positive cancer. (C) 2015 Elsevier Inc. All rights reserved.
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약학대학 (약학부)
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