Abstract |
We evaluated the anti- adult T-cell leukemia (ATL) effects of hippuristanol, an eukaryotic translation initiation inhibitor from the coral Isis hippuris. Hippuristanol inhibited proliferation of HTLV-1-infected T-cell lines and ATL cells, but not normal peripheral blood mononuclear cells. It induced cell cycle arrest during G₁ phase by reducing the expression of cyclin D1, cyclin D2, CDK4 and CDK6, and induced apoptosis by reducing the expression of Bcl-x(L), c-IAP2, XIAP and c-FLIP. The induced apoptosis was associated with activation of caspase-3, -8 and -9. Hippuristanol also suppressed IkappaBalpha phosphorylation and depleted IKKalpha, IKKgamma, JunB and JunD, resulting in inactivation of NF-kappaB and AP-1. It also suppressed carbonic anhydrase type II expression. In addition to its in vitro effects, hippuristanol suppressed tumor growth in mice with severe combined immunodeficiency harboring tumors induced by inoculation of HTLV-1-infected T cells. These preclinical data suggest that hippuristanol could be a potentially useful therapeutic agent for patients with ATL.
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Authors | Tomoyuki Tsumuraya, Chie Ishikawa, Yoshiaki Machijima, Sawako Nakachi, Masachika Senba, Junichi Tanaka, Naoki Mori |
Journal | Biochemical pharmacology
(Biochem Pharmacol)
Vol. 81
Issue 6
Pg. 713-22
(Mar 15 2011)
ISSN: 1873-2968 [Electronic] England |
PMID | 21219881
(Publication Type: Comparative Study, Journal Article)
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Copyright | Copyright © 2011 Elsevier Inc. All rights reserved. |
Chemical References |
- Enzyme Inhibitors
- Sterols
- hippuristanol
- Eukaryotic Initiation Factor-4A
- EIF4A3 protein, human
- DEAD-box RNA Helicases
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Topics |
- Animals
- Apoptosis
(drug effects, physiology)
- Cell Line, Transformed
- Cell Line, Tumor
- Cells, Cultured
- DEAD-box RNA Helicases
(antagonists & inhibitors, metabolism)
- Enzyme Inhibitors
(pharmacology, therapeutic use)
- Eukaryotic Initiation Factor-4A
- Female
- Human T-lymphotropic virus 1
(drug effects, physiology)
- Humans
- Leukemia-Lymphoma, Adult T-Cell
(drug therapy, metabolism, pathology)
- Mice
- Mice, Inbred ICR
- Mice, SCID
- Sterols
(pharmacology, therapeutic use)
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