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PMID: 16333034 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

OSW-1: a natural compound with potent anticancer activity and a novel mechanism of action.

Journal of the National Cancer Institute ·Vol. 97 ·No. 23 ·2005-12-07 ·Pages 1781-5

Zhou Y, Garcia-Prieto C, Carney DA, Xu RH, Pelicano H, Kang Y, Yu W, Lou C, Kondo S, Liu J, Harris DM, Estrov Z, Keating MJ, Jin Z, Huang P

Abstract

The naturally occurring compound 3beta,16beta,17alpha-trihydroxycholest-5-en-22-one 16-O-(2-O-4-methoxybenzoyl-beta-D-xylopyranosyl)-(1-->3)-(2-O-acetyl-alpha-L-arabinopyranoside) (OSW-1) is found in the bulbs of Ornithogalum saudersiae and is highly cytotoxic against tumor cell lines. Using various human cancer and nonmalignant cell lines, we investigated the anticancer activity and selectivity of OSW-1 and its underlying mechanisms of action. OSW-1 exhibited extremely potent cytotoxic activity against cancer cells in vitro. Nonmalignant cells were statistically significantly less sensitive to OSW-1 than cancer cells, with concentrations that cause a 50% loss of cell viability 40-150-fold greater than those observed in malignant cells. Electron microscopy and biochemical analyses revealed that OSW-1 damaged the mitochondrial membrane and cristae in both human leukemia and pancreatic cancer cells, leading to the loss of transmembrane potential, increase of cytosolic calcium, and activation of calcium-dependent apoptosis. Clones of leukemia cells with mitochondrial DNA defects and respiration deficiency that had adapted the ability to survive in culture without mitochondrial respiration also were resistant to OSW-1. In vitro analysis revealed that OSW-1 effectively killed primary leukemia cells from chronic lymphocytic leukemia patients with disease refractory to fludarabine. The promising anticancer activity of OSW-1 and its unique mechanism of action make this compound worthy of further investigation for its potential to overcome drug resistance.

MeSH Terms
Antineoplastic Agents/pharmacology Apoptosis/drug effects Calcium Channels/metabolism Cell Line, Tumor Cholestenones/pharmacology Drug Resistance, Neoplasm Humans Inhibitory Concentration 50 Leukemia, Lymphocytic, Chronic, B-Cell/drug therapy Microscopy, Electron Mitochondrial Membranes/drug effects Saponins/pharmacology Vidarabine/analogs & derivatives,pharmacology
Chemicals
Antineoplastic Agents Calcium Channels Cholestenones Saponins OSW 1 Vidarabine fludarabine
Authors & Affiliations
15 authors, click to expand affiliations / ORCID
Zhou Yan
Department of Molecular Pathology, The University of Texas M. D. Anderson Cancer Center, Houston, TX 77030, USA.
Garcia-Prieto Celia
Carney Dennis A
Xu Rui-hua
Pelicano Helene
Kang Ying
Yu Wensheng
Lou Changgang
Kondo Seiji
Liu Jinsong
Harris David M
Estrov Zeev
Keating Michael J
Jin Zhendong
Huang Peng
Article Info
Journal
Journal of the National Cancer Institute
Abbr.
J Natl Cancer Inst
ISSN
1460-2105
Published
2005-12-07
Pages
1781-5
Language
English
Region
United States
NLM ID
7503089
Subset
IM
Grants
NCI NIH HHS · CA105073 · United States
NCI NIH HHS · CA109041 · United States
NCI NIH HHS · CA16672 · United States
NCI NIH HHS · CA85563 · United States
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