前药
奥沙利铂
顺铂
化学
体内
癌症研究
血管生成
缺氧(环境)
碳酸酐酶
转移
癌细胞
肿瘤微环境
体外
生物化学
药理学
酶
癌症
化疗
医学
生物
内科学
肿瘤细胞
氧气
有机化学
结直肠癌
生物技术
作者
Qian Cao,Dan‐Jie Zhou,Zhengyin Pan,Gang Yang,Hang Zhang,Liang‐Nian Ji,Zong‐Wan Mao
标识
DOI:10.1002/anie.202005362
摘要
Abstract Hypoxia and the acidic microenvironment play a vital role in tumor metastasis and angiogenesis, generally compromising the chemotherapeutic efficacy. This provides a tantalizing angle for the design of platinum(IV) prodrugs for the effective and selective killing of solid tumors. Herein, two carbonic anhydrase IX (CAIX)‐targeting platinum(IV) prodrugs have been developed, named as CAIXplatins. Based on their strong affinity for and inhibition of CAIX, CAIXplatins can not only overcome hypoxia and the acidic microenvironment, but also inhibit metabolic pathways of hypoxic cancer cells, resulting in a significantly enhanced therapeutic effect on hypoxic MDA‐MB‐231 tumors both in vitro and in vivo compared with cisplatin/oxaliplatin, accompanied with excellent anti‐metastasis and anti‐angiogenesis activities. Furthermore, the cancer selectivity indexes of CAIXplatins are 70–90 times higher than those of cisplatin/oxaliplatin with effectively alleviated side‐effects.
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