| Literature DB >> 33440866 |
Hantae Jo1, Byungsun Cha2, Haneul Kim2, Sofia Brito1, Byeong Mun Kwak3,4, Sung Tae Kim5,6, Bum-Ho Bin1,2, Mi-Gi Lee7.
Abstract
Natural killer (NK) cells are lymphocytes that can directly destroy cancer cells. When NK cells are activated, CD56 and CD107a markers are able to recognize cancer cells and release perforin and granzyme B proteins that induce apoptosis in the targeted cells. In this study, we focused on the role of phytoncides in activating NK cells and promoting anticancer effects. We tested the effects of several phytoncide compounds on NK-92mi cells and demonstrated that α-pinene treatment exhibited higher anticancer effects, as observed by the increased levels of perforin, granzyme B, CD56 and CD107a. Furthermore, α-pinene treatment in NK-92mi cells increased NK cell cytotoxicity in two different cell lines, and immunoblot assays revealed that the ERK/AKT pathway is involved in NK cell cytotoxicity in response to phytoncides. Furthermore, CT-26 colon cancer cells were allografted subcutaneously into BALB/c mice, and α-pinene treatment then inhibited allografted tumor growth. Our findings demonstrate that α-pinene activates NK cells and increases NK cell cytotoxicity, suggesting it is a potential compound for cancer immunotherapy.Entities:
Keywords: ERK/AKT pathway; NK cell cytotoxicity; anticancer effect; natural killer cell; phytoncide; α-pinene
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Year: 2021 PMID: 33440866 PMCID: PMC7826552 DOI: 10.3390/ijms22020656
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923