RETRACTED ARTICLE: A water-soluble nucleolin aptamer-paclitaxel conjugate for tumor-specific targeting in ovarian cancer

Fangfei Li(Hong Kong Baptist University), Jun Lü(Hong Kong Baptist University), Jin Liu(Hong Kong Baptist University), Chao Liang(Hong Kong Baptist University), Maolin Wang(Hong Kong Baptist University), Luyao Wang(Hong Kong Baptist University), Defang Li(Hong Kong Baptist University), Houzong Yao(Hong Kong Baptist University), Qiulong Zhang(Hong Kong Baptist University), Jia Wen(Northwest A&F University), Zongkang Zhang(Chinese University of Hong Kong), Jie Li(Chinese University of Hong Kong), Quanxia Lv(Hong Kong Baptist University), Xiaojuan He(Hong Kong Baptist University), Baosheng Guo(Hong Kong Baptist University), Daogang Guan(Hong Kong Baptist University), Yuanyuan Yu(Hong Kong Baptist University), Lei Dang(Hong Kong Baptist University), Xiaohao Wu(Hong Kong Baptist University), Yongshu Li(Hong Kong Baptist University), Guofen Chen(Nanfang Hospital), Feng Jiang(Hong Kong Baptist University), Shiguo Sun(Northwest A&F University), Bao‐Ting Zhang(Chinese University of Hong Kong), Aiping Lü(Hong Kong Baptist University), Ge Zhang(Hong Kong Baptist University)
Nature Communications
November 3, 2017
Cited by 281Open Access
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Abstract

Paclitaxel (PTX) is among the most commonly used first-line drugs for cancer chemotherapy. However, its poor water solubility and indiscriminate distribution in normal tissues remain clinical challenges. Here we design and synthesize a highly water-soluble nucleolin aptamer-paclitaxel conjugate (NucA-PTX) that selectively delivers PTX to the tumor site. By connecting a tumor-targeting nucleolin aptamer (NucA) to the active hydroxyl group at 2' position of PTX via a cathepsin B sensitive dipeptide bond, NucA-PTX remains stable and inactive in the circulation. NucA facilitates the uptake of the conjugated PTX specifically in tumor cells. Once inside cells, the dipeptide bond linker of NucA-PTX is cleaved by cathepsin B and then the conjugated PTX is released for action. The NucA modification assists the selective accumulation of the conjugated PTX in ovarian tumor tissue rather than normal tissues, and subsequently resulting in notably improved antitumor activity and reduced toxicity.


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