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Published on: February 22, 2020
Bitter Melon Enhances Natural Killer-Mediated Toxicity against Head and Neck Cancer Cells
Sourav Bhattacharya1, Naoshad Muhammad1, Robert Steele1
1Department of Pathology, Saint Louis University, St. Louis, Missouri.
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.
Insights
Bitter melon extract (BME) enhances natural killer (NK) cell activity against head and neck squamous cell carcinoma (HNSCC). This study shows BME boosts NK-cell-mediated tumor killing, suggesting a role in cancer immunotherapy.
Area of Science:
- Immunology
- Oncology
- Natural Products
Background:
- Natural killer (NK) cells are crucial for innate immunity and antitumor responses.
- The role of NK cells in solid tumor growth control is under investigation.
- Bitter melon extract (BME) has been shown to modulate regulatory T cells in head and neck squamous cell carcinoma (HNSCC).
Purpose of the Study:
- To investigate the effect of BME on NK-cell-mediated killing of HNSCC cells.
- To determine if BME enhances the cytotoxic activity of NK cells against HNSCC.
Main Methods:
- Treatment of human NK-cell line (NK3.3) with BME.
- Co-culture of BME-treated NK3.3 cells with HNSCC cells.
- Analysis of NK cell degranulation markers (granzyme B, CD107a/LAMP1) and surface receptors (CD16, NKp30).
Main Results:
- BME treatment significantly enhanced the ability of NK3.3 cells to kill HNSCC cells.
- BME increased granzyme B accumulation and CD107a/LAMP1 translocation in NK3.3 cells.
- BME-treated NK3.3 cells exhibited increased surface expression of CD16 and NKp30 when co-cultured with HNSCC cells.
Conclusions:
- Bitter melon extract augments NK-cell-mediated killing activity against HNSCC.
- BME demonstrates an immunomodulatory role in enhancing NK cell function.
- These findings suggest BME as a potential therapeutic agent for HNSCC immunotherapy.
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