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利用金纳米颗粒使DNA修复沉默可使小儿脑肿瘤细胞对γ射线敏感。

Silencing of DNA repair sensitizes pediatric brain tumor cells to γ-irradiation using gold nanoparticles.

作者信息

Liu Zuliang, Yan Huiru, Li Hongsha

机构信息

Department of Pediatrics, Jiyang County People's Hospital, Ji'nan, Shandong 251400, China.

Department of Pediatrics, Jiyang County People's Hospital, Ji'nan, Shandong 251400, China.

出版信息

Environ Toxicol Pharmacol. 2017 Jul;53:40-45. doi: 10.1016/j.etap.2017.04.017. Epub 2017 Apr 27.

Abstract

We present a nanoparticle (NP)-mediated delivery vehicle that effectively carries and protects siRNA in pediatric ependymoma (EP) and medulloblastoma (MB) cells. The delivery vehicle consists of gold NPs coated with a polymeric shell comprising polyethylene glycol (PG), chitosan and polyethyleneimine (Au-CP-PEI). NPs loaded with siRNA knocked down Ape1 expression by over 75% in both MB and EP cells. Further, this reduction in Ape1 expression is associated with an increase in DNA damage after irradiation. The results indicate that NP-associated delivery of siApe1 is a feasible approach to circumventing pediatric brain tumor resistance to radiation therapy.

摘要

我们展示了一种纳米颗粒(NP)介导的递送载体,其能有效地在小儿室管膜瘤(EP)和髓母细胞瘤(MB)细胞中携带并保护小干扰RNA(siRNA)。该递送载体由包覆有包含聚乙二醇(PG)、壳聚糖和聚乙烯亚胺的聚合物外壳的金纳米颗粒(Au-CP-PEI)组成。装载有siRNA的纳米颗粒在MB和EP细胞中均使Ape1表达敲低超过75%。此外,Ape1表达的这种降低与辐射后DNA损伤的增加相关。结果表明,siApe1的NP相关递送是一种规避小儿脑肿瘤对放射治疗耐药性的可行方法。

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