Cell Death Pathway Regulation by Functional Nanomedicines for Robust Antitumor Immunity

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 anti...

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Main Authors: Yongjuan Li, Yichen Guo, Kaixin Zhang, Rongrong Zhu, Xiaoyuan Chen, Zhenzhong Zhang, Weijing Yang
Format: Article
Language:English
Published: Wiley 2024-01-01
Series:Advanced Science
Subjects:
Online Access:https://doi.org/10.1002/advs.202306580
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author Yongjuan Li
Yichen Guo
Kaixin Zhang
Rongrong Zhu
Xiaoyuan Chen
Zhenzhong Zhang
Weijing Yang
author_facet Yongjuan Li
Yichen Guo
Kaixin Zhang
Rongrong Zhu
Xiaoyuan Chen
Zhenzhong Zhang
Weijing Yang
author_sort Yongjuan Li
collection DOAJ
description 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.
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spelling doaj.art-9db26378869b427c88dc53e64225ef512024-01-19T09:27:54ZengWileyAdvanced Science2198-38442024-01-01113n/an/a10.1002/advs.202306580Cell Death Pathway Regulation by Functional Nanomedicines for Robust Antitumor ImmunityYongjuan Li0Yichen Guo1Kaixin Zhang2Rongrong Zhu3Xiaoyuan Chen4Zhenzhong Zhang5Weijing Yang6School of Pharmaceutical Sciences Henan Key Laboratory of Targeting Therapy and Diagnosis for Critical Diseases Zhengzhou University Zhengzhou Henan 450001 ChinaSchool of Pharmaceutical Sciences Henan Key Laboratory of Targeting Therapy and Diagnosis for Critical Diseases Zhengzhou University Zhengzhou Henan 450001 ChinaSchool of Pharmaceutical Sciences Henan Key Laboratory of Targeting Therapy and Diagnosis for Critical Diseases Zhengzhou University Zhengzhou Henan 450001 ChinaSchool of Pharmaceutical Sciences Henan Key Laboratory of Targeting Therapy and Diagnosis for Critical Diseases Zhengzhou University Zhengzhou Henan 450001 ChinaDepartments of Diagnostic Radiology, Surgery Chemical and Biomolecular Engineering, and Biomedical Engineering Yong Loo Lin School of Medicine and Faculty of Engineering National University of Singapore Singapore 119074 SingaporeSchool of Pharmaceutical Sciences Henan Key Laboratory of Targeting Therapy and Diagnosis for Critical Diseases Zhengzhou University Zhengzhou Henan 450001 ChinaSchool of Pharmaceutical Sciences Henan Key Laboratory of Targeting Therapy and Diagnosis for Critical Diseases Zhengzhou University Zhengzhou Henan 450001 ChinaAbstract 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.https://doi.org/10.1002/advs.202306580apoptosis and cuproptosisautophagy and necroptosiscancer immunotherapyferroptosis and pyroptosisnanomedicines
spellingShingle Yongjuan Li
Yichen Guo
Kaixin Zhang
Rongrong Zhu
Xiaoyuan Chen
Zhenzhong Zhang
Weijing Yang
Cell Death Pathway Regulation by Functional Nanomedicines for Robust Antitumor Immunity
Advanced Science
apoptosis and cuproptosis
autophagy and necroptosis
cancer immunotherapy
ferroptosis and pyroptosis
nanomedicines
title Cell Death Pathway Regulation by Functional Nanomedicines for Robust Antitumor Immunity
title_full Cell Death Pathway Regulation by Functional Nanomedicines for Robust Antitumor Immunity
title_fullStr Cell Death Pathway Regulation by Functional Nanomedicines for Robust Antitumor Immunity
title_full_unstemmed Cell Death Pathway Regulation by Functional Nanomedicines for Robust Antitumor Immunity
title_short Cell Death Pathway Regulation by Functional Nanomedicines for Robust Antitumor Immunity
title_sort cell death pathway regulation by functional nanomedicines for robust antitumor immunity
topic apoptosis and cuproptosis
autophagy and necroptosis
cancer immunotherapy
ferroptosis and pyroptosis
nanomedicines
url https://doi.org/10.1002/advs.202306580
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AT kaixinzhang celldeathpathwayregulationbyfunctionalnanomedicinesforrobustantitumorimmunity
AT rongrongzhu celldeathpathwayregulationbyfunctionalnanomedicinesforrobustantitumorimmunity
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