| Literature DB >> 28465362 |
Sourav Bhattacharya1, Naoshad Muhammad1, Robert Steele1, Jacki Kornbluth1,2, Ratna B Ray3.
Abstract
Natural killer (NK) cells are one of the major components of innate immunity, with the ability to mediate antitumor activity. Understanding the role of NK-cell-mediated tumor killing in controlling of solid tumor growth is still in the developmental stage. We have shown recently that bitter melon extract (BME) modulates the regulatory T cell (Treg) population in head and neck squamous cell carcinoma (HNSCC). However, the role of BME in NK-cell modulation against HNSCC remains unknown. In this study, we investigated whether BME can enhance the NK-cell killing activity against HNSCC cells. Our results indicated that treatment of human NK-cell line (NK3.3) with BME enhances ability to kill HNSCC cells. BME increases granzyme B accumulation and translocation/accumulation of CD107a/LAMP1 in NK3.3 cells exposed to BME. Furthermore, an increase in cell surface expression of CD16 and NKp30 in BME-treated NK3.3 cells was observed when cocultured with HNSCC cells. Collectively, our results demonstrated for the first time that BME augments NK-cell-mediated HNSCC killing activity, implicating an immunomodulatory role of BME. Cancer Prev Res; 10(6); 337-44. ©2017 AACR. ©2017 American Association for Cancer Research.Entities:
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Year: 2017 PMID: 28465362 PMCID: PMC5499682 DOI: 10.1158/1940-6207.CAPR-17-0046
Source DB: PubMed Journal: Cancer Prev Res (Phila) ISSN: 1940-6215