4.5 Article

Cytotoxic and PPARs transcriptional activities of sterols from the Vietnamese soft coral Lobophytum laevigatum

Journal

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
Volume 21, Issue 10, Pages 2845-2849

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmcl.2011.03.089

Keywords

Soft coral; Alcyoniidae; Lobophytum laevigatum; Cytotoxic; PPARs transcriptional; Lobophytosterol

Funding

  1. Vietnam's National Foundation for Science and Technology Development (NAFOSTED) [104.01.30.09]
  2. Priority Research Center through the National Research Foundation of Korea (NRF)
  3. Ministry of Education, Science and Technology, Republic of Korea [20090093815]
  4. National Research Foundation of Korea [과09B2106, 2009-0093815, 핵06A3304] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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A new unusual sterol, named lobophytosterol (1), and five known metabolites (2-6) were isolated from the methanol extract of the soft coral Lobophytum laevigatum. Their chemical structures were elucidated by extensive spectroscopic analysis and comparison with those reported in the literature. The absolute stereochemistry of 1 was determined using a modified Mosher's method. Compounds 1-3 showed cytotoxic activity against HCT-116 cells with IC50 values of 3.2, 6.9 and 18.1 mu M, respectively. Compound 1 additionally displayed cytotoxic effects on A549 and HL-60 cells with IC50 values of 4.5 and 5.6 mu M, respectively. Treatment of these cells with compound 1 resulted in an induction of apoptosis evident by chromatin condensation in treated cells. Besides, compounds 2, 4, and 6 significantly upregulated PPARs transcriptional activity dose-dependently in Hep-G2 cells. Taken together, these data suggest that compound 1 might inhibit the growth of the cancer cells by the induction of apoptosis, and compounds 2, 4, and 6 might act as specific agonists for PPAR alpha, PPAR delta, and PPAR gamma and may therefore regulate cellular glucose, lipid, and cholesterol metabolism. (C) 2011 Elsevier Ltd. All rights reserved.

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