sesterterpenoid and steroid metabolites from a deep-water alaska sponge inhibit wnt/β-catenin signaling in colon cancer cells

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ID: 211874
2018
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Abstract
The Wnt/β-catenin signaling pathway is known to play critical roles in a wide range of cellular processes: cell proliferation, differentiation, migration and embryonic development. Importantly, dysregulation of this pathway is tightly associated with pathogenesis in most human cancers. Therefore, the Wnt/β-catenin pathway has emerged as a promising target in anticancer drug screening programs. In the present study, we have isolated three previously unreported metabolites from an undescribed sponge, a species of Monanchora (Order Poecilosclerida, Family Crambidae), closely related to the northeastern Pacific species Monanchora pulchra, collected from deep waters off the Aleutian Islands of Alaska. Through an assortment of NMR, MS, ECD, computational chemical shifts calculation, and DP4, chemical structures of these metabolites have been characterized as spirocyclic ring-containing sesterterpenoid (1) and cholestane-type steroidal analogues (2 and 3). These compounds exhibited the inhibition of β-catenin response transcription (CRT) through the promotion of β-catenin degradation, which was in part implicated in the antiproliferative activity against two CRT-positive colon cancer cell lines.
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park2018marinesesterterpenoid Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors ;Hyun Bong Park;Nguyen Quoc Tuan;Joonseok Oh;Younglim Son;Mark T. Hamann;Robert Stone;Michelle Kelly;Sangtaek Oh;MinKyun Na
Journal jixie gongcheng xuebao/journal of mechanical engineering
Year 2018
DOI
10.3390/md16090297
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