吉西他滨
磷酰胺
化学
前药
胞苷脱氨酶
核苷
癌症研究
体内
核苷类似物
脱氧胞苷激酶
胞苷
体外
癌细胞
癌症
药理学
脱氧胞苷
生物化学
酶
生物
医学
内科学
生物技术
作者
Magdalena Ślusarczyk,Monica Huerta Lopez,Jan Balzarini,Malcolm D. Mason,Wen G. Jiang,Sarah P. Blagden,Emely Thompson,Essam Ghazaly,Christopher McGuigan
摘要
Gemcitabine is a nucleoside analogue commonly used in cancer therapy but with limited efficacy due to a high susceptibility to cancer cell resistance. The addition of a phosphoramidate motif to the gemcitabine can protect it against many of the key cancer resistance mechanisms. We have synthesized a series of gemcitabine phosphoramidate prodrugs and screened for cytostatic activity in a range of different tumor cell lines. Among the synthesized compounds, one in particular (NUC-1031, 6f) was shown to be potent in vitro. Importantly, compared with gemcitabine, 6f activation was significantly less dependent on deoxycytidine kinase and on nucleoside transporters, and it was resistant to cytidine deaminase-mediated degradation. Moreover, 6f showed a significant reduction in tumor volumes in vivo in pancreatic cancer xenografts. The ProTide 6f is now in clinical development with encouraging efficacy signals in a Phase I/II study, which strongly supports the ProTide approach to generate promising new anticancer agents.
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