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Xanthatin anti-tumor cytotoxicity is mediated via glycogen synthase kinase-3β and β-catenin.
- Source :
-
Biochemical pharmacology [Biochem Pharmacol] 2016 Sep 01; Vol. 115, pp. 18-27. Date of Electronic Publication: 2016 Jun 16. - Publication Year :
- 2016
-
Abstract
- Xanthatin, a xanthanolide sesquiterpene lactone isolated from Xanthium strumarium L. (Asteraceae), has prominent anti-tumor activity. Initial mechanism of action studies suggested xanthatin triggered activation of Wnt/β-catenin. We examined the effects of xanthatin on signaling pathways in A459 lung cancer cells and mouse embryonic fibroblasts to ascertain requirements for xanthatin-induced cell death and tumor growth in xenografts. Genetic inactivation of GSK-3β, but not the related isoform GSK-3α, compromised xanthatin cytotoxicity while inactivation of β-catenin enhanced xanthatin-mediated cell death. These data provide insight into how xanthatin and related molecules could be effectively targeted toward certain tumors.<br /> (Copyright © 2016 Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Cell Line, Tumor
Humans
Mice
Phosphorylation
Signal Transduction drug effects
Tumor Cells, Cultured
Xanthium chemistry
Antineoplastic Agents, Phytogenic pharmacology
Carcinoma, Non-Small-Cell Lung drug therapy
Furans pharmacology
Glycogen Synthase Kinase 3 beta metabolism
Lung Neoplasms drug therapy
beta Catenin metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1873-2968
- Volume :
- 115
- Database :
- MEDLINE
- Journal :
- Biochemical pharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 27321043
- Full Text :
- https://doi.org/10.1016/j.bcp.2016.06.009