4.7 Article

Ameliorative effect of atractylenolide III in the mast cell proliferation induced by TSLP

期刊

FOOD AND CHEMICAL TOXICOLOGY
卷 106, 期 -, 页码 78-85

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.fct.2017.05.042

关键词

Atractylenolide III; Mast cell; Thymic stromal lymphopoietin; Murine double minute 2; Signal transducer and activator of transcription 6; Interleukin-13

资金

  1. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Education, Science and Technology [2015R1A1A3A04000922]
  2. National Research Foundation of Korea [2015R1A1A3A04000922] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

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 pretreatment. Interleukin (1)-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, An-III decreased the TSLP-induced production of proinflammatory cytokines (IL-6, IL-1 beta, tumor necrosis factor-alpha, and IL-8). ATL-III decreased the levels of Bcl2 and procaspase-3 and increased caspase-3 activation and cleaved PARP levels. Furthermore, An-ill decreased TSLP-induced mast cell proliferation and the production of inflammatory cytokine by LAD2 cells. Taken together, these findings suggest that An-Ill plays a useful role as an anti-inflammatory agent and should be viewed as a potential anti-cancer agent. (C) 2017 Elsevier Ltd. All rights reserved.

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