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Enhanced natural killer cell anti-tumor activity with nanoparticles mediated ferroptosis and potential therapeutic application in prostate cancer
by
Choi, Hyunjun
, Kim, Kwang-Soo
, Kim, Dong-Hyun
, Ko, Min Jun
, Kim, Dong-Hwan
, Choi, Bongseo
in
Anticancer properties
/ Antitumor agents
/ Apoptosis
/ Biotechnology
/ Cancer therapies
/ Cancer therapy
/ Care and treatment
/ Cell activation
/ Cell death
/ Cell therapy
/ Chemistry
/ Chemistry and Materials Science
/ Cytotoxicity
/ Degranulation
/ Ferroptosis
/ Flow cytometry
/ Health aspects
/ HMGB1 protein
/ Immune system
/ Immunotherapy
/ Iron oxides
/ Killer cells
/ Ligands
/ Lipids
/ Lymphocytes
/ Molecular Medicine
/ Nanomedicine
/ Nanoparticles
/ Nanotechnology
/ Natural killer cells
/ NK cells
/ NKG2 antigen
/ PD-L1 protein
/ Physiological aspects
/ Prostate cancer
/ Proteins
/ Tumors
/ γ-Interferon
2022
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Enhanced natural killer cell anti-tumor activity with nanoparticles mediated ferroptosis and potential therapeutic application in prostate cancer
by
Choi, Hyunjun
, Kim, Kwang-Soo
, Kim, Dong-Hyun
, Ko, Min Jun
, Kim, Dong-Hwan
, Choi, Bongseo
in
Anticancer properties
/ Antitumor agents
/ Apoptosis
/ Biotechnology
/ Cancer therapies
/ Cancer therapy
/ Care and treatment
/ Cell activation
/ Cell death
/ Cell therapy
/ Chemistry
/ Chemistry and Materials Science
/ Cytotoxicity
/ Degranulation
/ Ferroptosis
/ Flow cytometry
/ Health aspects
/ HMGB1 protein
/ Immune system
/ Immunotherapy
/ Iron oxides
/ Killer cells
/ Ligands
/ Lipids
/ Lymphocytes
/ Molecular Medicine
/ Nanomedicine
/ Nanoparticles
/ Nanotechnology
/ Natural killer cells
/ NK cells
/ NKG2 antigen
/ PD-L1 protein
/ Physiological aspects
/ Prostate cancer
/ Proteins
/ Tumors
/ γ-Interferon
2022
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Enhanced natural killer cell anti-tumor activity with nanoparticles mediated ferroptosis and potential therapeutic application in prostate cancer
by
Choi, Hyunjun
, Kim, Kwang-Soo
, Kim, Dong-Hyun
, Ko, Min Jun
, Kim, Dong-Hwan
, Choi, Bongseo
in
Anticancer properties
/ Antitumor agents
/ Apoptosis
/ Biotechnology
/ Cancer therapies
/ Cancer therapy
/ Care and treatment
/ Cell activation
/ Cell death
/ Cell therapy
/ Chemistry
/ Chemistry and Materials Science
/ Cytotoxicity
/ Degranulation
/ Ferroptosis
/ Flow cytometry
/ Health aspects
/ HMGB1 protein
/ Immune system
/ Immunotherapy
/ Iron oxides
/ Killer cells
/ Ligands
/ Lipids
/ Lymphocytes
/ Molecular Medicine
/ Nanomedicine
/ Nanoparticles
/ Nanotechnology
/ Natural killer cells
/ NK cells
/ NKG2 antigen
/ PD-L1 protein
/ Physiological aspects
/ Prostate cancer
/ Proteins
/ Tumors
/ γ-Interferon
2022
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Enhanced natural killer cell anti-tumor activity with nanoparticles mediated ferroptosis and potential therapeutic application in prostate cancer
Journal Article
Enhanced natural killer cell anti-tumor activity with nanoparticles mediated ferroptosis and potential therapeutic application in prostate cancer
2022
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Overview
Ferroptosis provides an opportunity to overcome the cancer cell therapeutic resistance and modulate the immune system. Here an interaction between ferroptosis of cancer cells and natural killer (NK) cells was investigated with a clinical grade iron oxide nanoparticle (ferumoxytol) for potential synergistic anti-cancer effect of ferroptosis and NK cell therapy in prostate cancer. When ferumoxytol mediated ferroptosis of cancer cells was combined with NK cells, the NK cells’ cytotoxic function was increased. Observed ferroptosis mediated NK cell activation was also confirmed with IFN-γ secretion and lytic degranulation. Upregulation of ULBPs, which is one of the ligands for NK cell activating receptor NKG2D, was observed in the co-treatment of ferumoxytol mediated ferroptosis and NK cells. Additionally, HMGB1 and PD-L1 expression of cancer cells were observed in the treatment of ferroptosis + NK cells. Finally, in vivo therapeutic efficacy of ferumoxytol mediated ferroptosis and NK cell therapy was observed with significant tumor volume regression in a prostate cancer mice model. These results suggest that the NK cells’ function can be enhanced with ferumoxytol mediated ferroptosis.
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