Thapa Pritam, Li Mengjie, Bio Moses, Rajaputra Pallavi, Nkepang Gregory, Sun Yajing, Woo Sukyung, You Youngjae
College of Pharmacy, University of Oklahoma Health Sciences Center , 1110 North Stonewall Avenue, Oklahoma City, Oklahoma 73117, United States.
J Med Chem. 2016 Apr 14;59(7):3204-14. doi: 10.1021/acs.jmedchem.5b01971. Epub 2016 Mar 22.
Paclitaxel (PTX) is one of the most useful chemotherapeutic agents approved for several cancers, including ovarian, breast, pancreatic, and nonsmall cell lung cancer. However, it causes systemic side effects when administered parenterally. Photodynamic therapy (PDT) is a new strategy for treating local cancers using light and photosensitizer. Unfortunately, PDT is often followed by recurrence due to incomplete ablation of tumors. To overcome these problems, we prepared the far-red light-activatable prodrug of PTX by conjugating photosensitizer via singlet oxygen-cleavable aminoacrylate linker. Tubulin polymerization enhancement and cytotoxicity of prodrugs were dramatically reduced. However, once illuminated with far-red light, the prodrug effectively killed SKOV-3 ovarian cancer cells through the combined effects of PDT and locally released PTX. Ours is the first PTX prodrug that can be activated by singlet oxygen using tissue penetrable and clinically useful far-red light, which kills the cancer cells through the combined effects of PDT and site-specific PTX chemotherapy.
紫杉醇(PTX)是被批准用于多种癌症(包括卵巢癌、乳腺癌、胰腺癌和非小细胞肺癌)治疗的最有效的化疗药物之一。然而,经肠胃外给药时,它会引发全身性副作用。光动力疗法(PDT)是一种利用光和光敏剂治疗局部癌症的新策略。遗憾的是,由于肿瘤消融不完全,PDT治疗后常出现复发情况。为克服这些问题,我们通过单重态氧可裂解的氨基丙烯酸酯连接子将光敏剂与PTX共轭,制备了远红光可激活的PTX前药。前药的微管蛋白聚合增强作用和细胞毒性显著降低。然而,一旦用远红光照射,前药通过PDT和局部释放的PTX的联合作用有效杀死了SKOV - 3卵巢癌细胞。我们制备的是首个可利用组织穿透性且临床可用的远红光通过单重态氧激活的PTX前药,它通过PDT和位点特异性PTX化疗的联合作用杀死癌细胞。