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Anti-metastatic effects of antrodan, the Antrodia cinnamomea mycelia glycoprotein, in lung carcinoma cells. | LitMetric

Anti-metastatic effects of antrodan, the Antrodia cinnamomea mycelia glycoprotein, in lung carcinoma cells.

Int J Biol Macromol

Department of Food Science and Biotechnology, National Chung Hsing University, Taichung 402, Taiwan; Agricultural Biotechnology Center, National Chung Hsing University, Taichung 402, Taiwan. Electronic address:

Published: March 2015

AI Article Synopsis

  • Antrodan, a glycoprotein derived from Antrodia cinnamomea mycelia, was found to block invasion and migration of Lewis lung carcinoma (LLC) cells through increased expression of proteins that inhibit tumor metastasis.
  • The isolation of antrodan involved a multi-step purification process, leading to observed significant impacts on matrix metalloproteinases (MMP-2 and MMP-9) which are key players in cancer metastasis.
  • Additionally, antrodan's immunomodulatory effects were more pronounced than its direct actions, enhancing certain interleukins while suppressing others, ultimately suggesting its potential as a treatment against cancer spread.

Article Abstract

This study investigated the anti-metastatic effects of antrodan, the glycoprotein from Antrodia cinnamomea (AC) mycelia, through direct actions and indirect immunomodulatory effects in Lewis lung carcinoma (LLC). Antrodan was isolated from AC mycelia by alkali extraction, acid precipitation, and purification using sepharose CL-6B column chromatography. In the direct anti-metastatic action, antrodan (30-70 μg/mL) was found to significantly inhibit invasion and migration of LLC cells, and these effects involved up-regulation of tissue inhibitor of matrix metalloproteinase (TIMP)-1, TIMP-2, and nm23-H1 protein expression leading to decreased activities and protein expression of MMP-2 and MMP-9. For testing the indirect immunomodulatory effect, antrodan was incubated for 3d with mononuclear cells (MNCs) isolated from human peripheral blood to obtain the condition medium (CM). Antrodan significantly increased interleukin (IL)-12 and IL-1β levels, but decreased TNF-α, IL-6 and IL-8 levels in the MMC-CM, which also significantly inhibited invasion, migration, and the activities and protein expression of MMP-2 and MMP-9, but significantly increased protein expression of TIMP-1, TIMP-2, and nm23-H1 in LLC cells. The indirect immunomodulatory effect of antrodan was stronger than the direct anti-metastatic effect at the same concentrations (50 and 60 μg/mL). Overall, the results suggest the anti-metastatic potential of antrodan in LLC cells.

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Source
http://dx.doi.org/10.1016/j.ijbiomac.2015.01.004DOI Listing

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