肝细胞癌
癌症研究
更昔洛韦
转染
胸苷激酶
肝癌
医学
基因传递
乙型肝炎病毒
前药
单纯疱疹病毒
病毒
病毒学
药理学
化学
基因
人巨细胞病毒
生物化学
作者
Hannah J. Vaughan,Camila Gadens Zamboni,Laboni F. Hassan,Nicholas P. Radant,Desmond Jacob,Ronnie C. Mease,Il Minn,Stephany Y. Tzeng,Kathleen L. Gabrielson,Pranshu Bhardwaj,Xin Guo,David L. Francisco,Martin G. Pomper,Jordan J. Green
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2022-07-20
卷期号:8 (29)
被引量:32
标识
DOI:10.1126/sciadv.abo6406
摘要
Hepatocellular carcinoma (HCC) develops predominantly in the inflammatory environment of a cirrhotic liver caused by hepatitis, toxin exposure, or chronic liver disease. A targeted therapeutic approach is required to enable cancer killing without causing toxicity and liver failure. Poly(beta-amino-ester) (PBAE) nanoparticles (NPs) were used to deliver a completely CpG-free plasmid harboring mutant herpes simplex virus type 1 sr39 thymidine kinase (sr39) DNA to human HCC cells. Transfection with sr39 enables cancer cell killing with the prodrug ganciclovir and accumulation of 9-(4-
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