A chemotherapy nano-booster unlocks wider therapeutic window for prostate cancer treatment

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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Publication Details

Journal
Acta Pharmaceutica Sinica B
Published
2025-03-14
DOI
https://doi.org/10.1016/j.apsb.2025.03.029
Citations
2
Primary Topic
Nanoparticle-Based Drug Delivery
Type
article
Field-Weighted Citation Impact
1.19

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article

A chemotherapy nano-booster unlocks wider therapeutic window for prostate cancer treatment

Cong Luo, Shenwu Zhang, Ziqi Lin, Yuequan Wang et al.
2 citations
Acta Pharmaceutica Sinica B
Nanoparticle-Based Drug Delivery
1.19
article

A chemotherapy nano-booster unlocks wider therapeutic window for prostate cancer treatment

Cong Luo, Shenwu Zhang, Ziqi Lin, Yuequan Wang, Qin Chen, Yuting Wang, Hongyuan Zhang, Jin Sun, Rui Liao, Zhonggui He
article en
2 citations

Abstract

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.

Acta Pharmaceutica Sinica BVol. 15(6)
Shenyang Pharmaceutical University (CN), Liaoning Cancer Hospital & Institute (CN), China Medical University (CN)
National Natural Science Foundation of China, Department of Education of Liaoning Province, Shenyang Pharmaceutical University, Shenyang Young and Middle-aged Science and Technology Innovation Talent Support Program
Good health and well-being
Openalex Percentile: Top 24%
Nanoparticle-Based Drug Delivery
1.19
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