工程外泌体递送si-HER2和曲妥珠单抗治疗her2阳性胃癌的比较分析。

IF 2.7 3区 医学 Q2 ONCOLOGY
Yuehong Zhu, Yaoyang Guo, Ziyi Dong, Mingqing Zhang, Hui Liu, Xinyi Wen, Wenwen Pang, Xipeng Zhang, Zhansheng Jiang, Chong Chen, Jie Hao, Ming Gao, Haiyang Zhang
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引用次数: 0

摘要

曲妥珠单抗是目前治疗her2阳性胃癌(GC)的重点靶向药物,但在临床治疗中普遍存在耐药和心脏毒性等问题,导致治疗效果不佳。外泌体是药物传递的天然纳米载体,工程外泌体已广泛应用于转化医学研究。本研究旨在比较携带HER2 siRNA的工程外泌体和曲妥珠单抗的抗肿瘤作用和不良反应。利用慢病毒构建稳定的iRGD-293T细胞系,用si-HER2转染iRGD-293T和293T细胞,超离心分离外泌体。通过功能实验检测iRGD-exo-si-HER2和曲妥珠单抗对her2阳性GC细胞和小鼠异种移植模型的抑制作用。用血液生化指标检测毒副作用,特别是心脏毒性。iRGD肽修饰的工程外泌体在体外和体内均比对照外泌体具有更高的肿瘤亲和力。irgd -外泌体递送si-HER2可显著抑制HER2阳性GC细胞的增殖并促进其凋亡,iRGD-exo-si-HER2在体外和体内均可显著降低GC细胞中HER2的表达,其疗效与曲妥珠单抗相似,但心脏副作用更小。我们的数据表明,iRGD-exo-si-HER2在体内和体外均表现出良好的抗肿瘤效果,并且与曲妥珠单抗相比副作用更小。本研究提示,si-HER2工程外泌体可以作为治疗her2阳性胃癌的新策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative analysis of engineered-exosome delivered si-HER2 and trastuzumab in the treatment of HER2-positive gastric cancer.

Trastuzumab is currently a key targeted drug for HER2-positive gastric cancer (GC), but there are common problems of drug resistance and cardiotoxicity in clinical treatment, resulting in poor therapeutic effects. Exosomes are natural nanocarriers for drug delivery and engineered exosomes have been widely used in translational medicine research. This study is designed to compare the anti-tumor effects and adverse effects between engineered exosomes carrying HER2 siRNA and trastuzumab. The stable cell line of iRGD-293T was constructed by using lentiviruses, and iRGD-293T and 293T cells were transfected with si-HER2 and exosomes were isolated by ultra-centrifugation. Functional experiments were performed to examine the inhibitory effects of iRGD-exo-si-HER2 and trastuzumab on both HER2-positive GC cells and mouse xenograft models. Blood biochemical indexes were used to test the adverse effects, especially cardiotoxicity. The engineered exosomes modified by iRGD peptide showed higher tumor affinity compared to control exosomes in vitro and in vivo. si-HER2 delivered by iRGD-exosomes significantly inhibited the proliferation and promoted apoptosis of HER2-positive GC cells, and iRGD-exo-si-HER2 significantly reduced the expression of HER2 in GC cells in vitro and in vivo, showing similar efficacy as trastuzumab but with lower cardiac side effects. Our data indicated that iRGD-exo-si-HER2 shows good anti-tumor effect both in vivo and in vitro, and has fewer side effects compared with trastuzumab. And this study suggested that engineering exosomes with si-HER2 can serve as novel strategy for the treatment of HER2-positive GC.

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来源期刊
CiteScore
7.60
自引率
0.00%
发文量
121
审稿时长
1 months
期刊介绍: The development of new anticancer agents is one of the most rapidly changing aspects of cancer research. Investigational New Drugs provides a forum for the rapid dissemination of information on new anticancer agents. The papers published are of interest to the medical chemist, toxicologist, pharmacist, pharmacologist, biostatistician and clinical oncologist. Investigational New Drugs provides the fastest possible publication of new discoveries and results for the whole community of scientists developing anticancer agents.
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