Sodwanone and Yardenone Triterpenes from a South African Species of the Marine Sponge Axinella Inhibit Hypoxia-Inducible Factor-1 (HIF-1) Activation in Both Breast and Prostate Tumor Cells

Jingqiu Dai, James A. Fishback, Yu-Dong Zhou,* and Dale G. Nagle*
Department of Pharmacognosy, Research Institute of Pharmaceutical Sciences, School of Pharmacy, University of Mississippi, University, Mississippi 38677-1848
J. Nat. Prod., 2006, 69 (12), pp 1715–1720
DOI: 10.1021/np060278q
Publication Date (Web): November 17, 2006
Copyright © 2006 American Chemical Society and American Society of Pharmacognosy
*

 Corresponding authors. (Y.-D.Z.) Tel:  (662) 915-2012. Fax:  (662) 915-6975. E-mail:  ydzhou@olemiss.edu. (D.G.N.) Tel:  (662) 915-7026. Fax:  (662) 915-6975. E-mail:  dnagle@olemiss.edu.

Abstract

Abstract Image

Hypoxia-inducible factor-1 (HIF-1) is a transcription factor that promotes tumor cell adaptation and survival under hypoxic conditions. HIF-1 is currently recognized as an important molecular target for anticancer drug discovery. A T47D breast tumor cell-based reporter assay was used to evaluate the NCI Open Repository of marine invertebrates and algae lipid extracts for HIF-1 inhibitory activity. Bioassay-guided fractionation and isolation of an active extract from Axinella sp. yielded seven new sodwanone triterpenoids [3-epi-sodwanone K (1), 3-epi-sodwanone K 3-acetate (2), 10,11-dihydrosodwanone B (4), sodwanones T−W (3, 7, 8, 9)], the new yardenone triterpene 12R-hydroxyyardenone (10), and the previously reported compounds sodwanone A (5), sodwanone B (6), and yardenone (11). The structures and relative configurations of these Axinella metabolites were determined spectroscopically. The absolute configuration of 1 was determined by the modified Mosher ester procedure. Sodwanone V (8) inhibited both hypoxia-induced and iron chelator (1,10-phenanthroline)-induced HIF-1 activation in T47D breast tumor cells (IC50 15 μM), and 8 was the only sodwanone that inhibited HIF-1 activation in PC-3 prostate tumor cells (IC50 15 μM). Compounds 1, 3, 4, and 5 inhibited hypoxia-induced HIF-1 activation in T47D cells (IC50 values 20−25 μM). Compound 2 was cytotoxic to T47D cells (IC50 22 μM), and 8 showed cytotoxicity to MDA-MB-231 breast tumor cells (IC50 23 μM).

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History

  • Published In Issue December 27, 2006
  • Received June 12, 2006

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