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Arch Pharm Res ; 45(1): 1-10, 2022 Jan.
Article in English | MEDLINE | ID: mdl-34905179

ABSTRACT

The susceptibility of cancer cells to natural killer (NK) cell-mediated cytotoxicity depends on the balance of activating and inhibitory ligands expressed on their surface. Although many types of cancer cells are killed by NK cells, non-small-cell lung cancer (NSCLC) cells are relatively resistant to NK cell-mediated cytotoxicity. In this study, we showed that several NSCLC cell lines have differential sensitivity to NK cell-mediated cytotoxicity: NCI-H522 cells were highly sensitive, but A549, NCI-H23, NCI-H1915, and NCI-H1299 were resistant. Among activating ligands such as CD48, HLA-A/B/G, ICAM-1, MICA/B, and ULBPs, only CD48 rendered NCI-H522 cells susceptible to NK cell-mediated cytotoxicity, which was proved by using CD48 siRNA and neutralizing antibody. CD48-positive NCI-H522 cells established a more stable contact with NK cells than did CD48-negative A549 and CD48 siRNA cell-transfected NCI-H522 cells. Taken together, these data demonstrate that CD48-positive NSCLC cells might be susceptible to NK cell-mediated cytotoxicity, which provide information on how to stratify NSCLC patients potentially responsive to NK-cell therapy.


Subject(s)
CD48 Antigen/metabolism , Carcinoma, Non-Small-Cell Lung/immunology , Killer Cells, Natural/physiology , Lung Neoplasms/immunology , Blotting, Western , CD48 Antigen/immunology , Carcinoma, Non-Small-Cell Lung/metabolism , Cell Line, Tumor , Flow Cytometry , Humans , Killer Cells, Natural/immunology , Lung Neoplasms/metabolism , Polymerase Chain Reaction
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