CO-DELIVERY OF SIAPE1 AND MELATONIN BY 125I-LOADED PSMA-TARGETED NANOPARTICLES FOR THE TREATMENT OF PROSTATE CANCER

IF 2.4 3区 医学 Q3 ONCOLOGY
Ying Liu, Zhen-Duo Shi, Lin Hao, Yang Dong, Kun Pang, Xiao Hu, Cong-Hui Han
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引用次数: 0

Abstract

Introduction

Background: Both apurinic/apyrimidinic endodeoxyribonuclease 1 (APE1) inhibition and melatonin suppress prostate cancer (PCa) growth.

Objective

This study evaluated the therapeutic efficiency of self-assembled and prostate-specific membrane antigen (PSMA)-targeted nanocarrier loading 125I radioactive particles and encapsulat-ing siRNA targeting APE1 (siAPE1) and melatonin for PCa.

Methods

The linear polyarginine R12 polypeptide was prepared using Fmoc-Arg-Pbf-OH. The PSMA-targeted polymer was synthesized by conjugating azide-modified R12 peptide to PSMA monoclonal antibody (mAb). Before experiments, the PSMA-R12 nanocarrier was installed with melatonin and siAPE1, which were subsequently labeled by 125I radioactive particles. In vitro bio-compatibility and cytotoxicity of nanocomposites were examined in LNCaP cells and in vivo bio-distribution and pharmacokinetics were determined using PCa tumor-bearing mice.

Results

PSMA-R12 nanocarrier was ∼120 nm in size and was increased to ∼150 nm by melatonin encapsulation. PSMA-R12 nanoparticles had efficient loading capacities of siAPE1, melatonin, and 125I particles. The co-delivery of melatonin and siAPE1 by PSMA-R12-125I showed synergis-tic effects on suppressing LNCaP cell proliferation and Bcl-2 expression and promoting cell apop-tosis and caspase-3 expression. Pharmacokinetics analysis showed that Mel@PSMA-R12-125I particles had high uptake activity in the liver, spleen, kidney, intestine, and tumor, and were accumu-lated in the tumor sites within the first 8 h p.i., but was rapidly cleared from all the tested organs at 24 h p.i. Administration of nanoparticles to PCa tumors in vivo showed that Mel@PSMA-R12-125I/siAPE1 had high efficiency in suppressing PCa tumor growth.

Conclusions

The PSMA-targeted nanocarrier encapsulating siAPE1 and melatonin is a promising therapeutic strategy for PCa and can provide a theoretical basis for patent applications.
负载125i的psma靶向纳米颗粒共同递送siape1和褪黑素用于治疗前列腺癌
背景:无尿嘧啶/无嘧啶内源性脱氧核糖核酸酶1 (APE1)抑制和褪黑激素均可抑制前列腺癌(PCa)的生长。目的研究自组装前列腺特异性膜抗原(PSMA)靶向纳米载体装载125I放射性粒子并包封靶向APE1 (siAPE1)和褪黑激素的siRNA对前列腺癌的治疗效果。方法采用Fmoc-Arg-Pbf-OH法制备线性聚精氨酸R12多肽。通过叠氮化物修饰的R12肽与PSMA单克隆抗体(mAb)偶联合成PSMA靶向聚合物。实验前,在PSMA-R12纳米载体上安装褪黑激素和siAPE1,随后用125I放射性粒子标记。在LNCaP细胞中检测纳米复合材料的体外生物相容性和细胞毒性,并在前列腺癌荷瘤小鼠体内测定其生物分布和药代动力学。结果spsma - r12纳米载体尺寸为~ 120 nm,经褪黑素包封后增大至~ 150 nm。PSMA-R12纳米颗粒具有高效的siAPE1、褪黑素和125I颗粒的负载能力。PSMA-R12-125I共递送褪黑素和siAPE1,对抑制LNCaP细胞增殖和Bcl-2表达、促进细胞凋亡和caspase-3表达具有协同作用。药代动力学分析表明,Mel@PSMA-R12-125I颗粒在肝脏、脾脏、肾脏、肠道和肿瘤中具有较高的摄取活性,并在前8小时内积聚在肿瘤部位,但在24小时内迅速从所有受测器官中清除。体内给药于PCa肿瘤表明Mel@PSMA-R12-125I/siAPE1具有高效抑制PCa肿瘤生长的作用。结论psma靶向纳米载体包封siAPE1和褪黑素是一种有前景的PCa治疗策略,可为专利申请提供理论基础。
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来源期刊
CiteScore
4.80
自引率
3.70%
发文量
297
审稿时长
7.6 weeks
期刊介绍: Urologic Oncology: Seminars and Original Investigations is the official journal of the Society of Urologic Oncology. The journal publishes practical, timely, and relevant clinical and basic science research articles which address any aspect of urologic oncology. Each issue comprises original research, news and topics, survey articles providing short commentaries on other important articles in the urologic oncology literature, and reviews including an in-depth Seminar examining a specific clinical dilemma. The journal periodically publishes supplement issues devoted to areas of current interest to the urologic oncology community. Articles published are of interest to researchers and the clinicians involved in the practice of urologic oncology including urologists, oncologists, and radiologists.
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