CD48-expressing non-small-cell lung cancer cells are susceptible to natural killer cell-mediated cytotoxicity.
Eun Jae ParkHye Won JunIk Ho NaHong Kyung LeeJieun YunHyung Sook KimYoungsoo KimJin Tae HongSang-Bae HanPublished in: Archives of pharmacal research (2021)
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.
Keyphrases
- nk cells
- induced apoptosis
- cell cycle arrest
- cell therapy
- small cell lung cancer
- signaling pathway
- endoplasmic reticulum stress
- cell death
- stem cells
- machine learning
- chronic kidney disease
- healthcare
- newly diagnosed
- oxidative stress
- single cell
- end stage renal disease
- mass spectrometry
- advanced non small cell lung cancer
- cancer therapy
- cell proliferation
- high resolution
- deep learning
- social media
- pi k akt
- patient reported
- molecularly imprinted
- brain metastases