Laser-Ignited Lipid Peroxidation Nanoamplifiers for Strengthening Tumor Photodynamic Therapy Through Aggravating Ferroptotic Propagation and Sustainable High Immunogenicity

被引:20
作者
Ma, Yunong [1 ,2 ]
Zhao, Xi [1 ]
Tian, Peilin [1 ]
Xu, Kexin [1 ]
Luo, Jiayang [1 ]
Li, Honghui [2 ]
Yuan, Mingqing [1 ]
Liu, Xu [1 ]
Zhong, Yanping [3 ]
Wei, Pingzhen [3 ]
Song, Jiaxing [3 ]
Wen, Liewei [2 ]
Lu, Cuixia [1 ,4 ]
机构
[1] Guangxi Univ, Med Coll, Nanning 530004, Peoples R China
[2] Jinan Univ, Zhuhai Peoples Hosp, Zhuhai Hosp, Guangdong Prov Key Lab Tumor Intervent Diag & Trea, Zhuhai 519000, Peoples R China
[3] Guangxi Med Univ, Life Sci Inst, Med & Sci Res Ctr, Nanning 530021, Peoples R China
[4] Guangxi Univ, Sch Med, Guangxi Key Lab Special Biomed, Nanning 530004, Peoples R China
基金
中国国家自然科学基金;
关键词
anti-tumor immune response; ferroptosis; immunogenic cell death; lipid peroxidation; photodynamic therapy; COMBINATION; CANCER; NANOPARTICLES; PRODRUG; CHEMO;
D O I
10.1002/smll.202306402
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Photodynamic therapy (PDT) is extensively investigated for tumor therapy in the clinic. However, the efficacy of PDT is severely limited by the tissue penetrability of light, short effective half-life and radius of reactive oxygen species (ROS), and the weak immunostimulatory effect. In this study, a glutathione (GSH)-activatable nano-photosensitizer is developed to load with arachidonic acid (AA) and camouflage by erythrocyte membrane, which serves as a laser-ignited lipid peroxidation nanoamplifier (MAR). The photosensitive effect of MAR is recovered accompanied by the degradation in the tumor microenvironment and triggers the peroxidation of AA upon laser excitation. Interestingly, it aggravates the propagation of ferroptosis among cancer cells by driving the continuous lipid peroxidation chain reactions with the participation of the degradation products, ferrous ions (Fe2+), and AA. Consequently, even the deep-seated tumor cells without illumination also undergo ferroptosis owing to the propagation of ferroptotic signal. Moreover, the residual tumor cells undergoing ferroptosis still maintain high immunogenicity after PDT, thus continuously triggering sufficient tumor-associated antigens (TAAs) release to remarkably promote the anti-tumor immune response. Therefore, this study will provide a novel "all-in-one" nano-photosensitizer that not only amplifies the damaging effect and expands the effective range of PDT but also improves the immunostimulatory effect after PDT. A GSH-activatable nano-photosensitizer is developed to load with arachidonic acid, which serves as laser-ignited lipid peroxidation nano-amplifiers. It is able to aggravate the propagation of ferroptosis among cancer cells through driving the continuous lipid peroxidation chain reactions, which will potentiate the PDT. Particularly, the residual tumor cells undergoing ferroptosis still maintain high immunogenicity, thus continuously promote the anti-tumor immune response.image
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页数:15
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共 49 条
[1]   Photodynamic Therapy of Cancer: An Update [J].
Agostinis, Patrizia ;
Berg, Kristian ;
Cengel, Keith A. ;
Foster, Thomas H. ;
Girotti, Albert W. ;
Gollnick, Sandra O. ;
Hahn, Stephen M. ;
Hamblin, Michael R. ;
Juzeniene, Asta ;
Kessel, David ;
Korbelik, Mladen ;
Moan, Johan ;
Mroz, Pawel ;
Nowis, Dominika ;
Piette, Jacques ;
Wilson, Brian C. ;
Golab, Jakub .
CA-A CANCER JOURNAL FOR CLINICIANS, 2011, 61 (04) :250-281
[2]   Carrier-free nanoparticles of camptothecin prodrug for chemo-photothermal therapy: the making, in vitro and in vivo testing [J].
Ao, Mingtao ;
Yu, Fei ;
Li, Yixiang ;
Zhong, Mengya ;
Tang, Yonghe ;
Yang, Hua ;
Wu, Xiaojing ;
Zhuang, Yifan ;
Wang, Huiyun ;
Sun, Xiaolian ;
Hong, Xuehui ;
Chen, Xiao Dong .
JOURNAL OF NANOBIOTECHNOLOGY, 2021, 19 (01)
[3]   Immunogenic cell death inducer peptides: A new approach for cancer therapy, current status and future perspectives [J].
Aria, Hamid ;
Rezaei, Marzieh .
BIOMEDICINE & PHARMACOTHERAPY, 2023, 161
[4]   Photodynamic Therapy in Melanoma - Where do We Stand? [J].
Baldea, Ioana ;
Giurgiu, Lorin ;
Teacoe, Ioana Diana ;
Olteanu, Diana Elena ;
Olteanu, Florin Catalin ;
Clichici, Simona ;
Filip, Gabriela Adriana .
CURRENT MEDICINAL CHEMISTRY, 2018, 25 (40) :5540-5563
[5]   Photodynamic therapy and anti-tumour immunity [J].
Castano, Ana P. ;
Mroz, Pawel ;
Hamblin, Michael R. .
NATURE REVIEWS CANCER, 2006, 6 (07) :535-545
[6]   Immunogenic Cell Death and Role of Nanomaterials Serving as Therapeutic Vaccine for Personalized Cancer Immunotherapy [J].
Catanzaro, Elena ;
Feron, Olivier ;
Skirtach, Andre G. ;
Krysko, Dmitri V. .
FRONTIERS IN IMMUNOLOGY, 2022, 13
[7]   Gd2O3/b-TiO2 composite nanoprobes with ultra-high photoconversion efficiency for MR image-guided NIR-II photothermal therapy [J].
Chen, Jia ;
Chen, Tianxiang ;
Fang, Qianlan ;
Pan, Chunshu ;
Akakuru, Ozioma Udochukwu ;
Ren, Wenzhi ;
Lin, Jie ;
Sheng, Aizhu ;
Ma, Xuehua ;
Wu, Aiguo .
EXPLORATION, 2022, 2 (06)
[8]   Ferroptosis: machinery and regulation [J].
Chen, Xin ;
Li, Jingbo ;
Kang, Rui ;
Klionsky, Daniel J. ;
Tang, Daolin .
AUTOPHAGY, 2021, 17 (09) :2054-2081
[9]   Insight into the Prospects for Tumor Therapy Based on Photodynamic Immunotherapy [J].
Cheng, Xiaoxia ;
Wei, Yiqu ;
Jiang, Xiaomei ;
Wang, Chunli ;
Liu, Mengyu ;
Yan, Jiaxin ;
Zhang, Lei ;
Zhou, Yaqi .
PHARMACEUTICALS, 2022, 15 (11)
[10]   Immunogenic Cell Death: An Emerging Target in Gastrointestinal Cancers [J].
Chiaravalli, Marta ;
Spring, Alexia ;
Agostini, Antonio ;
Piro, Geny ;
Carbone, Carmine ;
Tortora, Giampaolo .
CELLS, 2022, 11 (19)