高尔基体
硫酸软骨素
前药
纳米颗粒
化学
软骨素
癌症研究
纳米技术
癌症
转移
糖胺聚糖
生物化学
材料科学
医学
细胞
内科学
作者
Haohuan Li,Pei Zhang,Jingwen Luo,Danrong Hu,Yuan Huang,Zhirong Zhang,Yao Fu,Tao Gong
出处
期刊:ACS Nano
[American Chemical Society]
日期:2019-08-02
卷期号:13 (8): 9386-9396
被引量:135
标识
DOI:10.1021/acsnano.9b04166
摘要
Metastasis is a multistep biological process regulated by multiple signaling pathways. The integrity of the Golgi apparatus plays an important role in these signaling pathways. Inspired by the mechanism and our previous finding about accumulation of chondroitin sulfate in Golgi apparatus in hepatic stellate cells, we developed a Golgi apparatus-targeting prodrug nanoparticle system by synthesizing retinoic acid (RA)-conjugated chondroitin sulfate (CS) (CS–RA). The prodrug nanoparticles appeared to accumulate in the Golgi apparatus in cancer cells and realized RA release under an acidic environment. We confirmed that CS–RA exhibited successful inhibition of multiple metastasis-associated proteins expression in vitro and in vivo by disruption of the Golgi apparatus structure. Following loading with paclitaxel (PTX), the CS–RA based nanoformulation (PTX–CS–RA) inhibited migration, invasion, and angiogenesis in vitro and suppressed tumor growth and metastasis in 4T1-Luc bearing mice. This multistep targeted nanoparticle system potentially enhanced the effect of antimetastasis combined with chemotherapy.
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