文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2025

纳米材料增强基于细胞焦亡的肿瘤免疫治疗。

Nanomaterials Enhance Pyroptosis-Based Tumor Immunotherapy.

机构信息

Department of Gastrointestinal and Colorectal Surgery, China-Japan Union Hospital of Jilin University, Changchun, 130033, People's Republic of China.

出版信息

Int J Nanomedicine. 2024 Jun 10;19:5545-5579. doi: 10.2147/IJN.S457309. eCollection 2024.


DOI:10.2147/IJN.S457309
PMID:38882539
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11178094/
Abstract

Pyroptosis, a pro-inflammatory and lytic programmed cell death pathway, possesses great potential for antitumor immunotherapy. By releasing cellular contents and a large number of pro-inflammatory factors, tumor cell pyroptosis can promote dendritic cell maturation, increase the intratumoral infiltration of cytotoxic T cells and natural killer cells, and reduce the number of immunosuppressive cells within the tumor. However, the efficient induction of pyroptosis and prevention of damage to normal tissues or cells is an urgent concern to be addressed. Recently, a wide variety of nanoplatforms have been designed to precisely trigger pyroptosis and activate the antitumor immune responses. This review provides an update on the progress in nanotechnology for enhancing pyroptosis-based tumor immunotherapy. Nanomaterials have shown great advantages in triggering pyroptosis by delivering pyroptosis initiators to tumors, increasing oxidative stress in tumor cells, and inducing intracellular osmotic pressure changes or ion imbalances. In addition, the challenges and future perspectives in this field are proposed to advance the clinical translation of pyroptosis-inducing nanomedicines.

摘要

细胞焦亡,一种促炎和裂解的程序性细胞死亡途径,在抗肿瘤免疫治疗方面具有巨大潜力。肿瘤细胞焦亡通过释放细胞内容物和大量促炎因子,促进树突状细胞成熟,增加肿瘤内细胞毒性 T 细胞和自然杀伤细胞的浸润,减少肿瘤内的免疫抑制细胞数量。然而,如何高效诱导细胞焦亡并防止对正常组织或细胞造成损伤是一个亟待解决的问题。最近,设计了多种纳米平台来精确触发细胞焦亡并激活抗肿瘤免疫反应。本综述介绍了纳米技术在增强基于细胞焦亡的肿瘤免疫治疗方面的最新进展。纳米材料在通过将细胞焦亡诱导剂递送至肿瘤、增加肿瘤细胞内氧化应激以及诱导细胞内渗透压变化或离子失衡来触发细胞焦亡方面显示出巨大优势。此外,还提出了该领域的挑战和未来展望,以推进诱导细胞焦亡的纳米药物的临床转化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c1/11178094/79f0ada72397/IJN-19-5545-g0010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c1/11178094/e7dbbf908ec2/IJN-19-5545-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c1/11178094/78f384d743ce/IJN-19-5545-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c1/11178094/5f3f287d91b8/IJN-19-5545-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c1/11178094/8a37ab922620/IJN-19-5545-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c1/11178094/0bb46e5695ab/IJN-19-5545-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c1/11178094/4af4dfd6ef21/IJN-19-5545-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c1/11178094/57a17a48463f/IJN-19-5545-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c1/11178094/20dfa86985e5/IJN-19-5545-g0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c1/11178094/4f8c34a4b1e4/IJN-19-5545-g0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c1/11178094/79f0ada72397/IJN-19-5545-g0010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c1/11178094/e7dbbf908ec2/IJN-19-5545-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c1/11178094/78f384d743ce/IJN-19-5545-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c1/11178094/5f3f287d91b8/IJN-19-5545-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c1/11178094/8a37ab922620/IJN-19-5545-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c1/11178094/0bb46e5695ab/IJN-19-5545-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c1/11178094/4af4dfd6ef21/IJN-19-5545-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c1/11178094/57a17a48463f/IJN-19-5545-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c1/11178094/20dfa86985e5/IJN-19-5545-g0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c1/11178094/4f8c34a4b1e4/IJN-19-5545-g0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c1/11178094/79f0ada72397/IJN-19-5545-g0010.jpg

相似文献

[1]
Nanomaterials Enhance Pyroptosis-Based Tumor Immunotherapy.

Int J Nanomedicine. 2024

[2]
Nanomedicine-induced cell pyroptosis to enhance antitumor immunotherapy.

J Mater Chem B. 2024-4-24

[3]
Programmed Cascade Polydopamine Nanoclusters for Pyroptosis-Based Tumor Immunotherapy.

Small. 2024-10

[4]
Nanoparticle-mediated cell pyroptosis: a new therapeutic strategy for inflammatory diseases and cancer.

J Nanobiotechnology. 2024-8-22

[5]
Tumor-Targeted Nanomedicine for Immunotherapy.

Acc Chem Res. 2020-12-15

[6]
Nanomedicine-Enabled/Augmented Cell Pyroptosis for Efficient Tumor Nanotherapy.

Adv Sci (Weinh). 2022-12

[7]
Combining Nanomedicine and Immunotherapy.

Acc Chem Res. 2019-5-23

[8]
Nanoscale Metal-Organic Frameworks for Cancer Immunotherapy.

Acc Chem Res. 2020-9-15

[9]
Dual-Responsive Supramolecular Polymeric Nanomedicine for Self-Cascade Amplified Cancer Immunotherapy.

Adv Sci (Weinh). 2024-5

[10]
Nanomedicine for T-Cell Mediated Immunotherapy.

Adv Mater. 2024-5

引用本文的文献

[1]
Nanotherapeutics induced redox resetting of oxidative and nitrosative stress: targeting glutathione-depletion in cancer.

Nanomedicine (Lond). 2025-5

[2]
Reactive Oxygen Species-Responsive Pyroptosis Nanoinitiators Promote Immune Cell Infiltration and Activate Anti-Tumor Immune Response.

Int J Nanomedicine. 2025-4-2

[3]
The Role and Therapeutic Potential of Pyroptosis in Colorectal Cancer: A Review.

Biomolecules. 2024-7-20

本文引用的文献

[1]
LncRNA Malat1 suppresses pyroptosis and T cell-mediated killing of incipient metastatic cells.

Nat Cancer. 2024-2

[2]
Nanomedicine Strategies in Conquering and Utilizing the Cancer Hypoxia Environment.

ACS Nano. 2023-11-14

[3]
Molecular mechanisms of pyroptosis and its role in anti-tumor immunity.

Int J Biol Sci. 2023

[4]
Targeting Pyroptosis through Lipopolysaccharide-Triggered Noncanonical Pathway for Safe and Efficient Cancer Immunotherapy.

Nano Lett. 2023-9-27

[5]
Saikosaponin-D induces the pyroptosis of lung cancer by increasing ROS and activating the NF-κB/NLRP3/caspase-1/GSDMD pathway.

J Biochem Mol Toxicol. 2023-8

[6]
Nigericin Boosts Anti-Tumor Immune Response via Inducing Pyroptosis in Triple-Negative Breast Cancer.

Cancers (Basel). 2023-6-16

[7]
The c-Src/LIST Positive Feedback Loop Sustains Tumor Progression and Chemoresistance.

Adv Sci (Weinh). 2023-7

[8]
Role of pyroptosis in the pathogenesis and treatment of diseases.

MedComm (2020). 2023-4-25

[9]
Alternative splicing of modulates killer lymphocyte-triggered pyroptosis.

Sci Immunol. 2023-4-28

[10]
Organoids technology for advancing the clinical translation of cancer nanomedicine.

Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2023

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

推荐工具

医学文档翻译智能文献检索