Bioresponsive antisense DNA gold nanobeacons as a hybrid in vivo theranostics platform for the inhibition of cancer cells and metastasis

被引:37
作者
Bao, Chenchen [1 ]
Conde, Joao [2 ,3 ]
Curtin, James [4 ]
Artzi, Natalie [2 ,5 ]
Tian, Furong [6 ]
Cui, Daxiang [1 ]
机构
[1] Shanghai Jiao Tong Univ, Natl Ctr Translat Med,Minist Educ, Sch Elect Informat & Elect Engn,Key Lab Thin Film, Inst Nano Biomed & Engn,Dept Instrument Sci & Eng, Shanghai 200030, Peoples R China
[2] MIT, Harvard Mit Div Hlth Sci & Technol, Inst Med Engn & Sci, Cambridge, MA 02139 USA
[3] Queen Mary Univ London, Sch Mat Sci & Engn, London, England
[4] Dublin Inst Technol, Coll Sci & Hlth, Sch Food Sci & Environm Hlth, Dublin, Ireland
[5] Harvard Univ, Brigham & Womens Hosp, Sch Med, Dept Anesthesiol, Boston, MA 02115 USA
[6] Dublin Inst Technol, Focas Res Inst, Dublin, Ireland
基金
爱尔兰科学基金会;
关键词
GASTRIC-CANCER; SPECTROSCOPIC ANALYSIS; LUNG; NANOPARTICLES; RAMAN; OLIGONUCLEOTIDES; MUTATIONS; ONCOGENE; THERAPY; BINDING;
D O I
10.1038/srep12297
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Gold nanobeacons can be used as a powerful tool for cancer theranostics. Here, we proposed a nanomaterial platform based on gold nanobeacons to detect, target and inhibit the expression of a mutant Kras gene in an in vivo murine gastric cancer model. The conjugation of fluorescently-labeled antisense DNA hairpin oligonucleotides to the surface of gold nanoparticles enables using their localized surface plasmon resonance properties to directly track the delivery to the primary gastric tumor and to lung metastatic sites. The fluorescently labeled nanobeacons reports on the interaction with the target as the fluorescent Cy3 signal is quenched by the gold nanoparticle and only emit light following conjugation to the Kras target owing to reorganization and opening of the nanobeacons, thus increasing the distance between the dye and the quencher. The systemic administration of the anti-Kras nanobeacons resulted in approximately 60% tumor size reduction and a 90% reduction in tumor vascularization. More important, the inhibition of the Kras gene expression in gastric tumors prevents the occurrence of metastasis to lung (80% reduction), increasing mice survival in more than 85%. Our developed platform can be easily adjusted to hybridize with any specific target and provide facile diagnosis and treatment for neoplastic diseases.
引用
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页数:13
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