Dendrimer-modified gold nanorods as a platform for combinational gene therapy and photothermal therapy of tumors.
Dendrimer-modified gold nanorods as a platform for combinational gene therapy and photothermal therapy of tumors.
复制标题
DOI:
10.1186/s13046-021-02105-3
复制
发表时间:
2021-09-27
期刊:
影响因子:
--
通讯作者:
Cui C
中科院分区:
文献类型:
--
作者:
Ye L;Chen Y;Mao J;Lei X;Yang Q;Cui C
The exploitation of novel nanomaterials combining diagnostic and therapeutic functionalities within one single nanoplatform is challenging for tumor theranostics. We synthesized dendrimer-modified gold nanorods for combinational gene therapy and photothermal therapy (PTT) of colon cancer. Poly(amidoamine) dendrimers (PAMAM, G3) grafted gold nanorods were modified with GX1 peptide (a cyclic 7-mer peptide, CGNSNPKSC). The obtained Au NR@PAMAM-GX1 are proposed as a gene delivery vector to gene (FAM172A, regulates the proliferation and apoptosis of colon cancer cells) for the combination of photothermal therapy (PTT) and gene therapy of Colon cancer cells (HCT-8 cells). In addition, the CT imaging function of Au NR can provide imaging evidence for the diagnosis of colon cancer. The results display that Au NR@PAMAM-GX1 can specifically deliver FAM172A to cancer cells with excellent transfection efficiency. The HCT-8 cells treated with the Au NR@PAMAM-GX1/FAM172A under laser irradiation have a viability of 20.45%, which is much lower than the survival rate of other single-mode PTT treatment or single-mode gene therapy. Furthermore, animal experiment results confirm that Au NR@PAMAM-GX1/FAM172A complexes can achieve tumor thermal imaging, targeted CT imaging, PTT and gene therapy after tail vein injection. Our findings demonstrate that the synthesized Au NR@PAMAM-GX1 offer a facile platform to exert antitumor and improve the diagnostic level of tumor. The online version contains supplementary material available at 10.1186/s13046-021-02105-3.
登录
查看更多内容
影响因子:
4.2
作者:
Qian K;Zhang J;Lu J;Liu W;Yao X;Chen Q;Lu S;Xiang G;Liu H
通讯作者:
Liu H
影响因子:
4.6
作者:
Hu Y;Wang R;Wang S;Ding L;Li J;Luo Y;Wang X;Shen M;Shi X
通讯作者:
Shi X
影响因子:
19
作者:
Liu, Jingjing;Wang, Chao;Liu, Zhuang
通讯作者:
Liu, Zhuang
影响因子:
17.1
作者:
Henderson, Luke;Neumann, Oara;Halas, Naomi J.
通讯作者:
Halas, Naomi J.
影响因子:
14
作者:
Lu, Qianglan;Lu, Tong;Li, Nan
通讯作者:
Li, Nan