A Robust ROS Generation and Ferroptotic Lipid Modulation Nanosystem for Mutual Reinforcement of Ferroptosis and Cancer Immunotherapy

被引:0
作者
Jiang, Chao [1 ,2 ,3 ,4 ]
Li, Wenxi [1 ,2 ,3 ]
Yan, Jie [1 ,2 ,3 ]
Yu, Xinying [1 ,2 ,3 ]
Feng, Yuzhao [1 ,2 ,3 ]
Li, Bei [1 ,2 ,3 ]
Liu, Yuan [4 ]
Dai, Yunlu [1 ,2 ,3 ]
机构
[1] Univ Macau, Fac Hlth Sci, Canc Ctr, Macau 999078, Peoples R China
[2] Univ Macau, Inst Translat Med, Fac Hlth Sci, Macau 999078, Peoples R China
[3] Univ Macau, MoE Frontiers Sci Ctr Precis Oncol, Macau 999078, Peoples R China
[4] Chinese Acad Sci, Zhejiang Canc Hosp, Hangzhou Inst Med HIM, Hangzhou 310022, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
cancer immunotherapy; ferroptosis; ferroptotic lipids; immunogenic cell death; reactive oxygen species; MECHANISMS; SUPPRESSION; THERAPY; CELLS;
D O I
10.1002/adhm.202401502
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Ferroptosis initiation is often utilized for synergistic immunotherapy. While, current immunotherapy is limited by an immunosuppressive tumor microenvironment (TME), and ferroptosis is limited by insufficient reactive oxygen species (ROS) and ferroptotic lipids in tumor cells. Here, an arachidonic acid (AA) loaded nanosystem (CTFAP) is developed to mutually reinforce ferroptosis and cancer immunotherapy by augmenting ROS generation and modulating ferroptotic lipids. CTFAP is composed of acid-responsive core calcium peroxide (CaO2) nanoparticles, ferroptotic lipids sponsor AA, tetracarboxylic porphyrin (TCPP) and Fe3+ based metal-organic framework structure, and biocompatible mPEG-DSPE for improved stability. Once endocytosed by tumor cells, CTFAP can release oxygen (O2) and hydrogen peroxide (H2O2) in the acidic TME, facilitating TCPP-based sonodynamic therapy and Fe3+-mediated Fenton-like reactions to generate substantial ROS for cell ferroptosis initiation. The immunogenic cell death (ICD) after ferroptosis promotes interferon gamma (IFN-gamma) secretion to up-regulate the expression of long-chain family member 4 (ACSL4), cooperating with the released AA from CTFAP to accelerate the accumulation of lipid peroxidation (LPO) and thereby promoting ferroptosis in cancer cells.CTFAP with ultrasound treatment efficiently suppresses tumor growth, has great potential to challenges in cancer immunotherapy. To mutually promote ferroptosis and cancer immunotherapy, a CaO2 core-based nanosystem (CTFAP) is developed to augment reactive oxygen species generation for ferroptosis initiation. Immunogenic cancer cell death promotes dendritic cell maturation and stimulates systemic antitumor immune responses to secrete IFN-gamma. The released IFN-gamma further up-regulates long-chain family member 4 expression, cooperating with the released arachidonic acid from the nanosystem in turn promoting cell ferroptosis. image
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页数:10
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共 54 条
  • [21] A platinum@polymer-catechol nanobraker enables radio-immunotherapy for crippling melanoma tumorigenesis, angiogenesis, and radioresistance
    Li, Wenxi
    Yan, Jie
    Tian, Hao
    Li, Bei
    Wang, Guohao
    Sang, Wei
    Zhang, Zhan
    Zhang, Xuanjun
    Dai, Yunlu
    [J]. BIOACTIVE MATERIALS, 2023, 22 : 34 - 46
  • [22] CD8+ T cells and fatty acids orchestrate tumor ferroptosis and immunity via ACSL4
    Liao, Peng
    Wang, Weimin
    Wang, Weichao
    Kryczek, Ilona
    Li, Xiong
    Bian, Yingjie
    Sell, Amanda
    Wei, Shuang
    Grove, Sara
    Johnson, Jeffrey K.
    Kennedy, Paul D.
    Gijon, Miguel
    Shah, Yatrik M.
    Zou, Weiping
    [J]. CANCER CELL, 2022, 40 (04) : 365 - +
  • [23] Liu J., 2024, ADV MATER, V36
  • [24] The critical role and molecular mechanisms of ferroptosis in antioxidant systems: a narrative review
    Liu, Meng
    Kong, Xiao-Yu
    Yao, Yuan
    Wang, Xin-An
    Yang, Wei
    Wu, Hui
    Li, Song
    Ding, Jia-Wang
    Yang, Jian
    [J]. ANNALS OF TRANSLATIONAL MEDICINE, 2022, 10 (06)
  • [25] Iron-Containing Protein-Mimic Supramolecular Iron Delivery Systems for Ferroptosis Tumor Therapy
    Liu, Shuwei
    Zhang, Mengsi
    Jin, Hao
    Wang, Ze
    Liu, Yi
    Zhang, Songling
    Zhang, Hao
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2023, 145 (01) : 160 - 170
  • [26] Multi-enzyme Co-expressed Dual-Atom Nanozymes Induce Cascade Immunogenic Ferroptosis via Activating Interferon-? and Targeting Arachidonic Acid Metabolism
    Liu, Yang
    Niu, Rui
    Deng, Ruiping
    Song, Shuyan
    Wang, Yinghui
    Zhang, Hongjie
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2023, 145 (16) : 8965 - 8978
  • [27] Reversing Ferroptosis Resistance in Breast Cancer via Tailored Lipid and Iron Presentation
    Luo, Jiajia
    Li, Yao
    Li, Yaru
    Chen, Xuefei
    Du, Panyu
    Wang, Zheng
    Tian, Aixian
    Zhao, Yanjun
    [J]. ACS NANO, 2023, 17 (24) : 25257 - 25268
  • [28] Ma Y., 2024, SMALL, V20
  • [29] Ferroptosis, a new form of cell death: opportunities and challenges in cancer
    Mou, Yanhua
    Wang, Jun
    Wu, Jinchun
    He, Dan
    Zhang, Chunfang
    Duan, Chaojun
    Li, Bin
    [J]. JOURNAL OF HEMATOLOGY & ONCOLOGY, 2019, 12
  • [30] Bioactive Iridium Nanoclusters with Glutathione Depletion Ability for Enhanced Sonodynamic-Triggered Ferroptosis-Like Cancer Cell Death
    Nie, Tongtong
    Zou, Weijuan
    Meng, Zheying
    Wang, Longchen
    Ying, Tao
    Cai, Xiaojun
    Wu, Jianrong
    Zheng, Yuanyi
    Hu, Bing
    [J]. ADVANCED MATERIALS, 2022, 34 (45)