基于DP7-C的新型全身siDR6递送系统治疗转移性肺癌

IF 6.6 2区 医学 Q1 NANOSCIENCE & NANOTECHNOLOGY
International Journal of Nanomedicine Pub Date : 2025-03-19 eCollection Date: 2025-01-01 DOI:10.2147/IJN.S488213
Hongyou Zhou, Rui Zhang, Ke Men, Lin Tang, Yusi Wang, Li Yang
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引用次数: 0

摘要

背景:转移性肺癌是许多原发性癌症的常见并发症,其治疗历来是一个重大的临床挑战。一旦发生肺转移,患者的生存期往往明显缩短。因此,预防和治疗肺转移是癌症治疗的一个重要方面。在这项研究中,一种简单、低毒、胆固醇修饰的阳离子细胞穿透肽DP7 (DP7- c)联合siDR6用于静脉给药治疗肺转移瘤。方法:首先分析临床数据库,确定转移性肿瘤中死亡受体6 (death receptor 6, DR6)的表达水平以及DR6表达与患者生存时间的相关性。采用自组装法制备了DP7-C/siDR6胶束。通过体外培养293T、B16F10和LL2细胞,评估DP7-C/siDR6的转染效率、安全性和抗癌能力,并通过小鼠实验考察其对肺部的靶向性和预防作用。此外,DP7-C/siDR6在原位肺癌LL2模型、人工肺转移B16F10模型和自发性肺转移4T1模型中均显示出治疗效果。结果:临床数据分析显示,DR6在大多数转移性肿瘤中高表达,高表达患者的生存期明显缩短。DP7-C/siDR6转染效率高,可通过抑制STAT3信号通路抑制肿瘤细胞生长。随后的小鼠实验表明,静脉注射DP7-C/siDR6可有效靶向肺部。研究发现,抑制肺内皮细胞DR6的表达可阻止转移性肺内皮细胞原发性坏死,从而阻止肿瘤转移。DP7-C/siDR6治疗在肿瘤模型中表现出良好的治疗效果。结论:携带siDR6的DP7-C胶束的全身递送提供了一种阻止肺癌肺转移的替代治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Novel Systemic siDR6 Delivery System Based on DP7-C for the Treatment of Metastatic Lung Cancer.

Background: The treatment of metastatic lung cancer, a common complication of many primary cancers, has historically been a significant clinical challenge. Once lung metastasis occurs, patients' survival is often significantly shortened. Therefore, prevention and treatment of lung metastases is an important aspect of cancer treatment. In this study, a simple, low-toxicity, cholesterol-modified cationic cell-penetrating peptide DP7 (DP7-C), in combination with siDR6 was used for intravenous administration for the treatment of lung metastases.

Methods: Initially, clinical databases were analyzed to determine the expression levels of death receptor 6 (DR6) in metastatic tumors and the correlation between DR6 expression and patient survival times. The DP7-C/siDR6 micelles were prepared by a self-assembly method. By cultivating 293T, B16F10 and LL2 cells, the in vitro experiments were performed to assess the transfection efficiency, safety and anti-cancer ability of DP7-C/siDR6, while its targeting efficiency and prevention of lungs were investigated by mouse experiments. Furthermore, the therapeutic efficacy of DP7-C/siDR6 was demonstrated in the LL2 model of lung cancer in situ, the B16F10 model of artificial lung metastasis, and the 4T1 model of spontaneous lung metastasis.

Results: The clinical data analysis revealed that DR6 was highly expressed in the majority of metastatic tumors and that patients with high DR6 expression exhibited significantly shorter survival times. The DP7-C/siDR6 showed high transfection efficiency, and it could inhibit tumor cell growth by suppressing the STAT3 signaling pathway. Subsequent mouse experiments demonstrated that intravenous administration of DP7-C/siDR6 resulted in efficient lung targeting. The inhibition of DR6 expression on lung endothelial cells was found to prevent metastasis-induced primary necrosis of lung endothelial cells, thereby preventing tumor metastasis. And the DP7-C/siDR6 treatment showed excellent therapeutic efficacy in the tumor models.

Conclusion: The systemic delivery of DP7-C micelles carrying siDR6 provide an alternative therapeutic strategy to halt cancer lung metastasis.

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来源期刊
International Journal of Nanomedicine
International Journal of Nanomedicine NANOSCIENCE & NANOTECHNOLOGY-PHARMACOLOGY & PHARMACY
CiteScore
14.40
自引率
3.80%
发文量
511
审稿时长
1.4 months
期刊介绍: The International Journal of Nanomedicine is a globally recognized journal that focuses on the applications of nanotechnology in the biomedical field. It is a peer-reviewed and open-access publication that covers diverse aspects of this rapidly evolving research area. With its strong emphasis on the clinical potential of nanoparticles in disease diagnostics, prevention, and treatment, the journal aims to showcase cutting-edge research and development in the field. Starting from now, the International Journal of Nanomedicine will not accept meta-analyses for publication.
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