Recent Advances in Nanomaterial-Mediated Cell Death for Cancer Therapy

被引:2
作者
Luo, Min [1 ]
Wang, Yuan-min [1 ]
Zhao, Fu-kun [1 ]
Luo, Yong [2 ]
机构
[1] Zunyi Med Univ, Affiliated Hosp 3, Peoples Hosp Zunyi 1, Dept Clin Med, Zunyi 563000, Guizhou, Peoples R China
[2] Zunyi Med Univ, Affiliated Hosp 3, Peoples Hosp Zunyi 1, Dept Neurol, Zunyi 563000, Guizhou, Peoples R China
关键词
cancer; cell death; nanomaterial; UNFOLDED PROTEIN RESPONSE; DRUG-DELIVERY; EMERGING MECHANISMS; AUTOPHAGY PROMOTES; STRESS-RESPONSE; MONTE-CARLO; DNA-DAMAGE; IN-VITRO; APOPTOSIS; FERROPTOSIS;
D O I
10.1002/adhm.202402697
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Nanomedicine has shown great anticancer potential by disrupting redox homeostasis and increasing the levels of oxidative stress, but the therapeutic effect is limited by factors including the intrinsic self-protection mechanism of tumors. Cancer cell death can be induced by the exploration of different cell death mechanisms, such as apoptosis, pyroptosis, necroptosis, cuproptosis, and ferroptosis. The merging of nanotechnology with biomedicine has provided tremendous opportunities to construct cell death-based nanomedicine for innovative cancer therapy. Nanocarriers are not only used for the targeted delivery of cell death inducers, but also as therapeutic components to induce cell death to achieve efficient tumor treatment. This review focuses on seven cell death modalities mediated by nanomaterials, such as apoptosis, pyroptosis, necroptosis, ferroptosis, cuprotosis, immunogenic cell death, and autophagy. The mechanisms of these seven cell death modalities are described in detail, as well as the preparation of nanomaterials that induce them and the mechanisms, they used to exert their effects. Finally, this work describes the potential future development based on the current knowledge related to cell death induced by nanomaterials.
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页数:32
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共 256 条
  • [1] Abdelwahab S. A., 2020, QJM-INT J MED, V113
  • [2] Targeting immunogenic cell death in cancer
    Ahmed, Asma
    Tait, Stephen W. G.
    [J]. MOLECULAR ONCOLOGY, 2020, 14 (12) : 2994 - 3006
  • [3] Extrinsic Phagocyte-Dependent STING Signaling Dictates the Immunogenicity of Dying Cells
    Ahn, Jeonghyun
    Xia, Tianli
    Capote, Ailem Rabasa
    Betancourt, Dillon
    Barber, Glen N.
    [J]. CANCER CELL, 2018, 33 (05) : 862 - +
  • [4] Next-generation engineered nanogold for multimodal cancer therapy and imaging: a clinical perspectives
    Alle, Madhusudhan
    Sharma, Garima
    Lee, Seung-Hwan
    Kim, Jin-Chul
    [J]. JOURNAL OF NANOBIOTECHNOLOGY, 2022, 20 (01)
  • [5] Inflammasome-mediated inflammation and fibrosis: It is more than just the IL-1
    Amir, Muhammad
    Czaja, Mark J.
    [J]. HEPATOLOGY, 2018, 67 (02) : 479 - 481
  • [6] The Warburg effect modulates DHODH role in ferroptosis: a review
    Amos, Alvan
    Amos, Alex
    Wu, Lirong
    Xia, He
    [J]. CELL COMMUNICATION AND SIGNALING, 2023, 21 (01)
  • [7] H-ferritin suppression and pronounced mitochondrial respiration make Hepatocellular Carcinoma cells sensitive to RSL3-induced ferroptosis
    Asperti, Michela
    Bellini, Sonia
    Grillo, Elisabetta
    Gryzik, Magdalena
    Cantamessa, Luca
    Ronca, Roberto
    Maccarinelli, Federica
    Salvi, Alessandro
    De Petro, Giuseppina
    Arosio, Paolo
    Mitola, Stefania
    Poli, Maura
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 2021, 169 : 294 - 303
  • [8] Forgotten Pioneers of Plastic and Reconstructive Surgery During the Medieval Period
    Atiyeh, Bishara
    Habal, Mutaz B.
    [J]. JOURNAL OF CRANIOFACIAL SURGERY, 2023, 34 (03) : 1144 - 1146
  • [9] BANNAI S, 1980, J BIOL CHEM, V255, P2372
  • [10] Battaglioni D. B., 2022, CELL, V185, P1814