前列腺癌
治疗窗口
医学
助推器(火箭)
窗口(计算)
肿瘤科
化疗
癌症
内科学
计算机科学
工程类
药理学
万维网
航空航天工程
作者
Rui Liao,Yuequan Wang,Ziqi Lin,Yuting Wang,Hongyuan Zhang,Qin Chen,Shenwu Zhang,Jin Sun,Zhonggui He,Cong Luo
标识
DOI:10.1016/j.apsb.2025.03.029
摘要
Clinical chemotherapy for prostate cancer is still compromised by high treatment thresholds and severe off-target toxicity of drugs. Given the limited progress in improving therapeutic outcomes and reducing toxicity with the existing toolbox, efforts to broaden the chemotherapeutic window are highly desired. Here, we discover that gossypol (GSP, a natural compound) dramatically enhances the chemosensitivity of cabazitaxel (CTX), even at previously ineffective concentrations. Based on this interesting finding, we exploit a carrier-free chemotherapeutic nano-booster for prostate cancer treatment, which is molecularly co-assembled by GSP and cabazitaxel (CTX). GSP not only readily forms nanoassembly with CTX, but also functions as a chemotherapeutic enhancer that unlocks an ultra-low-dose chemotherapeutic window. Not only that, precise dual-drug nanoassembly confers CTX a significantly larger maximum tolerable dose. As expected, the nano-booster exerts striking therapeutic benefits in mouse prostate tumor xenograft models. This study advances chemotherapeutic window expansion and self-sensitized chemotherapy toward clinical applicability.
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