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功能纳米药物调控细胞死亡通路以增强抗肿瘤免疫

Cell Death Pathway Regulation by Functional Nanomedicines for Robust Antitumor Immunity.

机构信息

School of Pharmaceutical Sciences, Henan Key Laboratory of Targeting Therapy and Diagnosis for Critical Diseases, Zhengzhou University, Zhengzhou, Henan, 450001, China.

Medical Research Center, The First Affiliated Hospital of Zhengzhou University, Zhengzhou University, Zhengzhou, Henan, 450001, China.

出版信息

Adv Sci (Weinh). 2024 Jan;11(3):e2306580. doi: 10.1002/advs.202306580. Epub 2023 Nov 20.

Abstract

Cancer immunotherapy has become a mainstream cancer treatment over traditional therapeutic modes. Cancer cells can undergo programmed cell death including ferroptosis, pyroptosis, autophagy, necroptosis, apoptosis and cuproptosis which are find to have intrinsic relationships with host antitumor immune response. However, direct use of cell death inducers or regulators may bring about severe side effects that can also be rapidly excreted and degraded with low therapeutic efficacy. Nanomaterials are able to carry them for long circulation time, high tumor accumulation and controlled release to achieve satisfactory therapeutic effect. Nowadays, a large number of studies have focused on nanomedicines-based strategies through modulating cell death modalities to potentiate antitumor immunity. Herein, immune cell types and their function are first summarized, and state-of-the-art research progresses in nanomedicines mediated cell death pathways (e.g., ferroptosis, pyroptosis, autophagy, necroptosis, apoptosis and cuproptosis) with immune response provocation are highlighted. Subsequently, the conclusion and outlook of potential research focus are discussed.

摘要

癌症免疫疗法已成为一种主流的癌症治疗方法,优于传统的治疗模式。癌细胞可以经历程序性细胞死亡,包括铁死亡、细胞焦亡、自噬、坏死性凋亡、细胞凋亡和铜死亡,这些发现与宿主抗肿瘤免疫反应有内在关系。然而,直接使用细胞死亡诱导剂或调节剂可能会带来严重的副作用,而且它们的治疗效果也很低,还可能会迅速被排泄和降解。纳米材料能够延长它们的循环时间、提高肿瘤积累和控制释放,以达到令人满意的治疗效果。如今,大量的研究集中在基于纳米医学的策略上,通过调节细胞死亡方式来增强抗肿瘤免疫。在此,首先总结了免疫细胞类型及其功能,并强调了纳米医学介导的细胞死亡途径(如铁死亡、细胞焦亡、自噬、坏死性凋亡、细胞凋亡和铜死亡)与免疫反应激发的最新研究进展。随后,讨论了潜在研究重点的结论和展望。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5a5/10797449/47eb40285144/ADVS-11-2306580-g010.jpg

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