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克唑替尼前药胶束共递送阿霉素用于乳腺癌化疗免疫治疗中协同诱导免疫原性细胞死亡。

Crizotinib prodrug micelles co-delivered doxorubicin for synergistic immunogenic cell death induction on breast cancer chemo-immunotherapy.

作者信息

Liang Qiangwei, Lan Yang, Li Yifan, Cao Yongjin, Li Juan, Liu Yanhua

机构信息

Department of Pharmaceutics, School of Pharmacy, Ningxia Medical University, No. 1160, Shengli Street, Yinchuan 750004, China.

Department of Pharmaceutics, School of Pharmacy, Ningxia Medical University, No. 1160, Shengli Street, Yinchuan 750004, China; Key Laboratory of Hui Ethnic Medicine Modernization, Ningxia Medical University, Yinchuan 750004, China.

出版信息

Eur J Pharm Biopharm. 2022 Aug;177:260-272. doi: 10.1016/j.ejpb.2022.07.006. Epub 2022 Jul 18.


DOI:10.1016/j.ejpb.2022.07.006
PMID:35863668
Abstract

Chemotherapeutic agents can trigger the immune response via inducing immunogenic cell death (ICD), but the weak ICD effect induced by chemotherapy alone limits its lasting antitumor immunotherapy effect. A Cro polymerized prodrug carriers (POEG-b-PCro) with immunostimulatory by ICD induction was developed and co-delivered DOX to generate synergistic ICD induction for chemo-immunotherapy on breast cancer. DOX/POEG-b-PCro micelles displayed prolonged circulation in blood, efficient accumulation in tumors, internalization and then co-released DOX&Cro in tumor cells. Moreover, the DOX/POEG-b-PCro micelles synergistically triggered ICD induction by releasing the nuclear high mobility group box 1 (HMGB1) and down-regulation of c-Met level for generating chemo-immune anti-tumor actions. Importantly, the DOX/POEG-b-PCro micelles synergistically enhanced the tumor cytotoxic T lymphocytes infiltration, concomitant decreasing the immunosuppressive regulatory T (Treg) cells, accompanied with the increased cytokines secretion of IFN-γ and TNF-α, consequently displaying an improved anti-tumor activity in 4 T1 breast cancer mice. Overall, POEG-b-PCro prodrug micelles co-delivered DOX could be served as a promising nano drug delivery system for synergistic ICD induction on breast cancer chemo-immunotherapy.

摘要

化疗药物可通过诱导免疫原性细胞死亡(ICD)触发免疫反应,但单纯化疗诱导的ICD效应较弱,限制了其持久的抗肿瘤免疫治疗效果。开发了一种通过ICD诱导具有免疫刺激作用的克罗聚合物前药载体(POEG-b-PCro),并共同递送阿霉素以产生协同ICD诱导作用,用于乳腺癌的化学免疫治疗。阿霉素/POEG-b-PCro胶束在血液中循环时间延长,在肿瘤中有效蓄积,内化后在肿瘤细胞中共释放阿霉素和克罗。此外,阿霉素/POEG-b-PCro胶束通过释放核高迁移率族蛋白B1(HMGB1)和下调c-Met水平协同触发ICD诱导,以产生化学免疫抗肿瘤作用。重要的是,阿霉素/POEG-b-PCro胶束协同增强肿瘤细胞毒性T淋巴细胞浸润,同时减少免疫抑制调节性T(Treg)细胞,伴随着干扰素-γ和肿瘤坏死因子-α细胞因子分泌增加,因此在4T1乳腺癌小鼠中显示出改善的抗肿瘤活性。总体而言,共同递送阿霉素的POEG-b-PCro前药胶束可作为一种有前景的纳米药物递送系统,用于乳腺癌化学免疫治疗的协同ICD诱导。

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[2]
How has the field of immunogenic cell death in breast cancer evolved and impacted clinical practice over the past eleven years?

Hum Vaccin Immunother. 2025-12

[3]
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Front Immunol. 2024-11-27

[4]
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[5]
Comprehensive review of drug-mediated ICD inhibition of breast cancer: mechanism, status, and prospects.

Clin Exp Med. 2024-9-26

[6]
4-Deoxy--Pyrromycinone: A Promising Drug/Lead Compound to Treat Tumors.

Drug Des Devel Ther. 2024

[7]
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J Nanobiotechnology. 2024-6-8

[8]
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Acta Pharm Sin B. 2024-6

[9]
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[10]
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