替莫唑胺
前药
癌症研究
奥沙利铂
胶质瘤
化学
药物输送
抗药性
药理学
药品
生物
医学
生物化学
癌症
内科学
结直肠癌
有机化学
微生物学
作者
Yongheng Wang,Yuhang Jiang,Dengshuai Wei,Priya Singh,Yingjie Yu,Teresa Lee,Lingpu Zhang,Hanna K. Mandl,Alexandra S. Piotrowski-Daspit,Xinyuan Chen,Fan Li,Xing Li,Yiyu Cheng,Alexander Josowitz,Fan Yang,Yao Zhao,Fuyi Wang,Zhenwen Zhao,Anita Hüttner,Ranjit S. Bindra,Haihua Xiao,W. Mark Saltzman
标识
DOI:10.1038/s41551-021-00728-7
摘要
In patients with glioblastoma, resistance to the chemotherapeutic temozolomide (TMZ) limits any survival benefits conferred by the drug. Here we show that the convection-enhanced delivery of nanoparticles containing disulfide bonds (which are cleaved in the reductive environment of the tumour) and encapsulating an oxaliplatin prodrug and a cationic DNA intercalator inhibit the growth of TMZ-resistant cells from patient-derived xenografts, and hinder the progression of TMZ-resistant human glioblastoma tumours in mice without causing any detectable toxicity. Genome-wide RNA profiling and metabolomic analyses of a glioma cell line treated with the cationic intercalator or with TMZ showed substantial differences in the signalling and metabolic pathways altered by each drug. Our findings suggest that the combination of anticancer drugs with distinct mechanisms of action with selective drug release and convection-enhanced delivery may represent a translational strategy for the treatment of TMZ-resistant gliomas.
科研通智能强力驱动
Strongly Powered by AbleSci AI