| Literature DB >> 28545868 |
Myoung-Schook Yoou1, Sun-Young Nam1, Mu Hyun Jin2, So Young Lee2, Mi-Sun Kim2, Seok Seon Roh3, In Hwa Choi4, Nariyah Woo5, SeokWon Lim5, Dong Hyun Kim5, Jae-Bum Jang6, Hyung-Min Kim7, Hyun-Ja Jeong8.
Abstract
Atractylenolide III (ATL-III) is an active compound of Atractylodes lancea, which has been widely used for the treatment of cancer. Cancer is closely connected with inflammation, and many anti-inflammatory agents are also used to treat cancer. We investigated the influence of ATL-III on thymic stromal lymphopoietin (TSLP)-induced inflammatory reactions. Pretreatment with ATL-III suppressed murine double minute 2 levels and promoted p53 levels in TSLP-treated human mast cell, HMC-1 cells. Mast cell proliferation increased by TSLP or IL-3 stimulation was significantly decreased by ATL-III pretreatment. Interleukin (IL)-13 and phosphorylated signal transducer and activator of transcription 3, 5, and 6 levels in TSLP-treated HMC-1 cells were also decreased by ATL-III pretreatment. In addition, ATL-III decreased the TSLP-induced production of proinflammatory cytokines (IL-6, IL-1β, tumor necrosis factor-α, and IL-8). ATL-III decreased the levels of Bcl2 and procaspase-3 and increased caspase-3 activation and cleaved PARP levels. Furthermore, ATL-III decreased TSLP-induced mast cell proliferation and the production of inflammatory cytokine by LAD2 cells. Taken together, these findings suggest that ATL-III plays a useful role as an anti-inflammatory agent and should be viewed as a potential anti-cancer agent.Entities:
Keywords: Atractylenolide III; Interleukin-13; Mast cell; Murine double minute 2; Signal transducer and activator of transcription 6; Thymic stromal lymphopoietin
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Year: 2017 PMID: 28545868 DOI: 10.1016/j.fct.2017.05.042
Source DB: PubMed Journal: Food Chem Toxicol ISSN: 0278-6915 Impact factor: 6.023