前列腺癌
内化
癌症研究
谷氨酸羧肽酶Ⅱ
卡波扎尼布
化学
药物输送
靶向治疗
癌症
医学
药理学
细胞
内科学
生物化学
血管内皮生长因子受体
有机化学
作者
Anu Rani,Anunay J. Pulukuri,Jing Wei,Anubhav Dhull,Aqib Iqbal Dar,Rishi Sharma,Nooshin Mesbahi,Emily A. Savoy,Hosog Yoon,Boyang Jason Wu,Clifford E. Berkman,Anjali Sharma
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2024-08-21
卷期号:25 (9): 6164-6180
标识
DOI:10.1021/acs.biomac.4c00878
摘要
Prostate cancer (PC) is the fifth leading cause of cancer-related deaths among men worldwide. Prostate-specific membrane antigen (PSMA), a molecular target of PC, is clinically used for the treatment and diagnosis of PC using radioligand approaches. However, no PSMA-based chemotherapies have yet been approved by the FDA. Here, we present a novel therapeutic approach using PSMA-targeted 2-deoxyglucose-dendrimer (PSMA-2DG-D) for targeted delivery of a potent tyrosine kinase inhibitor, cabozantinib (Cabo), selectively to PC cells. PSMA-2DG-D demonstrates intracellular localization in PSMA (+) PC cells through PSMA-mediated internalization. This PSMA-specific targeting translates to enhanced efficacy of Cabo compared to the free drug when conjugated to PSMA-2DG-D. Furthermore, systemically administered fluorescently labeled PSMA-2DG-D-Cy5 specifically targets PSMA (+) tumors with minimal off-target accumulation in the PC3-PIP tumor xenograft mouse model. This demonstrates that the PSMA-2DG-D platform is a promising new delivery system for potent chemotherapeutics, where systemic side effects are a significant concern.
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