阿霉素
前列腺癌
靶向给药
前列腺
烯醇化酶
内化
癌症研究
体内
脂质体
医学
癌症
细胞毒性
靶向治疗
药物输送
药品
化疗
药理学
化学
内科学
体外
生物
免疫组织化学
生物化学
受体
有机化学
生物技术
作者
Luyao Wang,Mengke Qu,Shiqi Huang,Yu Fu,Liuqing Yang,Shanshan He,Lin Li,Zhirong Zhang,Qing Lin,Ling Zhang
出处
期刊:Nanoscale
[Royal Society of Chemistry]
日期:2018-01-01
卷期号:10 (28): 13673-13683
被引量:37
摘要
Prostate cancer, one of the leading causes of disease and death in men all over the world, is challenging to treat. α-Enolase, a multifunctional protein, is overexpressed on human prostate carcinoma cells, and thereby it is a potential target for treatment of prostate cancer. In the current study, the pHCT74 peptide was used to construct a kind of highly targeted liposome (pHCT74-lipo) loaded with doxorubicin (pHCT74-lipo-Dox), which specifically targeted α-enolase on prostate tumour cells. Compared with liposomes without pHCT74 modification, pHCT74-lipo-Dox displayed a superior intracellular internalization with enhanced tumour cytotoxicity. In the in vivo study, pHCT74-lipo showed much higher tumour accumulation. In addition, loaded into pHCT74-lipo, doxorubicin demonstrated significantly improved anti-tumour activity on prostate tumour-bearing mice. These results suggest that the pHCT74 peptide has potential to be used in the development of a novel drug delivery system for targeted therapy against prostate cancer.
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