Effective delivery of p65 shRNA by optimized Tween 85-polyethyleneimine conjugate for inhibition of tumor growth and lymphatic metastasis
文献类型:期刊论文
作者 | Xiao, Jisheng2; Duan, Xiaopin1,2; Meng, Qingshuo2; Yin, Qi2![]() ![]() ![]() ![]() ![]() ![]() |
刊名 | ACTA BIOMATERIALIA
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出版日期 | 2014-06 |
卷号 | 10期号:6页码:2674-2683 |
关键词 | Tween 85-PEI conjugates p65 shRNA Lymphatic metastasis Breast cancer Nanoparticles |
ISSN号 | 1742-7061 |
DOI | 10.1016/j.actbio.2014.02.009 |
文献子类 | Article |
英文摘要 | To maximize the interference efficacy of pGPU6/Neo-p65 shRNA-expressing pDNA (p65 shRNA) and subsequently more effectively inhibit tumor growth and lymphatic metastasis through blocking the nuclear factor-kappa B (NF-kappa B) signaling pathway, seven Tween 85-polyethyleneimine (PEI) conjugates (TnPs, n = 2, 3, 4, 5, 6, 7 and 8), which differed in the length of the polymethylene [-(CH2)(n)-] spacer between Tween 85 and PEI, were synthesized and investigated. The results showed that the transfection efficiency and cytotoxicity both increased with the spacer chain length. Then, TnPs with a [-(CH2)(6)-] spacer (T6P) were chosen to deliver p65 shRNA to a tumor and subsequently inhibit tumor growth and lymphatic metastasis. The T6P/p65 shRNA complex nanoparticles (T(6)Ns) could significantly down-regulate p65 expression in breast cancer cells, and consequently inhibit cell invasion and disrupt the tube formation. Most importantly, T(6)Ns accumulated greatly in tumor tissue, and as a result, significantly inhibited the growth and lymphatic metastasis of breast cancer xenograft. All these results indicated that the transfection efficacies of cationic amphiphiles could be significantly modulated by minor structural variations, and that T6P was promising for the effective delivery of p65 shRNA to knock down the expression of the key metastasis-driving genes and inhibit tumor growth and metastasis. (C) 2014 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved. |
WOS关键词 | NF-KAPPA-B ; GENE-TRANSFER EFFICACIES ; BREAST-CANCER ; TRANSFECTION PROPERTIES ; CATIONIC AMPHIPHILES ; SERUM COMPATIBILITY ; INVASION ; CELLS ; LIPIDS ; ANGIOGENESIS |
资助项目 | National Basic Research Program of China[2010CB934000] ; National Basic Research Program of China[2013CB932503] ; National Natural Science Foundation of China[81230029] ; National Natural Science Foundation of China[81270047] ; Shanghai Program[12nm 0501300] |
WOS研究方向 | Engineering ; Materials Science |
语种 | 英语 |
WOS记录号 | WOS:000336345900031 |
出版者 | ELSEVIER SCI LTD |
源URL | [http://119.78.100.183/handle/2S10ELR8/277054] ![]() |
专题 | 药物制剂研究中心 |
通讯作者 | Li, Yaping |
作者单位 | 1.Shenyang Pharmaceut Univ, Sch Pharm, Shenyang 110016, Peoples R China 2.Chinese Acad Sci, Shanghai Inst Mat Med, Ctr Pharmaceut, Shanghai 201203, Peoples R China; |
推荐引用方式 GB/T 7714 | Xiao, Jisheng,Duan, Xiaopin,Meng, Qingshuo,et al. Effective delivery of p65 shRNA by optimized Tween 85-polyethyleneimine conjugate for inhibition of tumor growth and lymphatic metastasis[J]. ACTA BIOMATERIALIA,2014,10(6):2674-2683. |
APA | Xiao, Jisheng.,Duan, Xiaopin.,Meng, Qingshuo.,Yin, Qi.,Zhang, Zhiwen.,...&Li, Yaping.(2014).Effective delivery of p65 shRNA by optimized Tween 85-polyethyleneimine conjugate for inhibition of tumor growth and lymphatic metastasis.ACTA BIOMATERIALIA,10(6),2674-2683. |
MLA | Xiao, Jisheng,et al."Effective delivery of p65 shRNA by optimized Tween 85-polyethyleneimine conjugate for inhibition of tumor growth and lymphatic metastasis".ACTA BIOMATERIALIA 10.6(2014):2674-2683. |
入库方式: OAI收割
来源:上海药物研究所
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