A novel prostate cancer-specific fluorescent probe based on extracellular vesicles targeting STEAP1 applied in fluorescence guided surgery

IF 11.5 1区 医学 Q1 CHEMISTRY, MULTIDISCIPLINARY Journal of Controlled Release Pub Date : 2025-02-05 DOI:10.1016/j.jconrel.2025.01.079
Jian-Xuan Sun , Qi-Dong Xia , Jin-Zhou Xu , Ye An , Si-Yang Ma , Jing-Yu Xu , Jia-Cheng Xiang , Chen-Qian Liu , Meng-Yao Xu , Si-Han Zhang , Yang Luan , Ke Tang , Shao-Gang Wang
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Abstract

Radical prostatectomy with pelvic lymph node dissection is the best treatment for intermediate- to high-risk localized prostate cancer (PCa). However, conventional white light surgery has difficulties in identifying tumor boundary and micrometastases intraoperatively. Fluorescence guided surgery (FGS) can solve the above difficulties, but lacks tumor-specific near-infrared fluorescent (NIRF) probes in PCa. STEAP1 was an ideal target in PCa treatment and imaging. Here, we constructed a PCa specific fluorescent probe based on extracellular vesicles targeting STEAP1 (AS-EVs) loaded with NIRF dye S0456 and evaluated its preclinical profiles. In vitro and in vivo studies both showed S0456@AS-EVs was safe and showed strong targeting ability to PCa in various mice xenograft models. S0456@AS-EVs could clear rapidly from blood (half-time of 4.29 h) and retain in the STEAP1 positive tumor tissues for more than 72 h with the highest tumor background ratio (TBR) of 3:1, which was superior to ICG, free S0456, ICG@Ctrl-EVs and S0456@Ctrl-EVs (p < 0.01). Finally, S0456@AS-EVs was applied in FGS on intramuscular model, and the tumors were resected under white light and fluorescence respectively. Compared with white light surgery, mice undergoing FGS had lower positive margin rate and better postoperative survival (p = 0.0342).

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基于细胞外囊泡靶向STEAP1的前列腺癌特异性荧光探针在荧光引导手术中的应用
根治性前列腺切除术加盆腔淋巴结清扫是治疗中高危局限性前列腺癌的最佳方法。然而,传统的白光手术在识别肿瘤边界和术中微转移方面存在困难。荧光引导手术(FGS)可以解决上述困难,但在前列腺癌中缺乏肿瘤特异性的近红外荧光(NIRF)探针。STEAP1是前列腺癌治疗和成像的理想靶点。在这里,我们构建了一个基于细胞外囊泡的PCa特异性荧光探针,靶向装载NIRF染料S0456的STEAP1 (as - ev),并评估了其临床前特征。体外和体内研究均表明S0456@AS-EVs在各种小鼠异种移植模型中是安全的,并且对PCa具有很强的靶向能力。S0456@AS-EVs可快速从血液中清除(半衰期为4.29 h),并在STEAP1阳性肿瘤组织中保留72 h以上,最高肿瘤背景比(TBR)为3:1,优于ICG、游离S0456、ICG@Ctrl-EVs和S0456@Ctrl-EVs (p
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来源期刊
Journal of Controlled Release
Journal of Controlled Release 医学-化学综合
CiteScore
18.50
自引率
5.60%
发文量
700
审稿时长
39 days
期刊介绍: The Journal of Controlled Release (JCR) proudly serves as the Official Journal of the Controlled Release Society and the Japan Society of Drug Delivery System. Dedicated to the broad field of delivery science and technology, JCR publishes high-quality research articles covering drug delivery systems and all facets of formulations. This includes the physicochemical and biological properties of drugs, design and characterization of dosage forms, release mechanisms, in vivo testing, and formulation research and development across pharmaceutical, diagnostic, agricultural, environmental, cosmetic, and food industries. Priority is given to manuscripts that contribute to the fundamental understanding of principles or demonstrate the advantages of novel technologies in terms of safety and efficacy over current clinical standards. JCR strives to be a leading platform for advancements in delivery science and technology.
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