DNA Nanorobot Delivers Antisense Oligonucleotides Silencing c-Met Gene Expression for Cancer Therapy

被引:9
作者
Zhang, Xiaolin [1 ]
Liu, Nanxin [1 ]
Zhou, Mi [1 ]
Zhang, Tao [1 ]
Tian, Taoran [1 ]
Li, Songhang [1 ]
Tang, Zisheng [2 ]
Lin, Yunfeng [1 ]
Cai, Xiaoxiao [1 ]
机构
[1] Sichuan Univ, West China Hosp Stomatol, Natl Clin Res Ctr Oral Dis, State Key Lab Oral Dis, Chengdu 610041, Sichuan, Peoples R China
[2] Shanghai Jiao Tong Univ, Shanghai Peoples Hosp 9, Sch Med, Dept Endodont,Coll Stomatol, Shanghai 200011, Peoples R China
基金
中国国家自然科学基金;
关键词
tFNA; Antisense Oligonucleotides; Cell Migration; HGF/c-Met Signaling Pathway; Cancer Therapy; TYROSINE KINASE; NANOSTRUCTURES; PROLIFERATION; RATIONALE; APTAMER; RNA;
D O I
10.1166/jbn.2019.2828
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Antisense oligonucleotides are considered to be a promising strategy for cancer therapy because of their high specificity and minimal side effects. They can bind specifically to mRNA silencing the expression of target genes. However, ssDNA cannot enter cells in large quantities, which limits its applications. Tetrahedral framework nucleic acids (tFNA) are considered to be optimal nanoscopic drug carriers because of their editability and biocompatibility. Most importantly, they can be modified with functional molecules. The over-expression of c-Met is associated with a wide variety of tumor occurrences, developments, drug resistance and prognoses. Activation of HGF/c-Met signaling pathways can promote cell migration and invasion in cancer. Therefore, blocking the expression of c-Met is a valid technique for cancer therapy. In this study. we used tFNA as carriers to deliver antisense oligonucleotides, which can bind to c-Met mRNA with high specificity and affinity, into cells resulting in the inhibition of c-Met expression for cancer therapy.
引用
收藏
页码:1948 / 1959
页数:12
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