RRC ID 43184
著者 Kashiwagi K, Harada K, Yano Y, Kumadaki I, Hagiwara K, Takebayashi J, Kido W, Virgona N, Yano T.
タイトル A redox-silent analogue of tocotrienol inhibits hypoxic adaptation of lung cancer cells.
ジャーナル Biochem Biophys Res Commun
Abstract We have previously reported that a redox-silent analogue of alpha-tocotrienol (T3), 6-O-carboxypropyl-alpha-tocotrienol (T3E) shows more potential anti-carcinogenic property than T3 in a lung cancer cell (A549 cell). However, the mechanisms by which T3E exerts its potential anti-carcinogenic effect is still unclear. As tumor malignancy is associated with hypoxia adaptation, in this study, we examined whether T3E could suppress survival and invasion in A549 cells under hypoxia. Hypoxia treatment drastically-induced activation of the protein tyrosine kinase, Src, and its regulated signaling required for hypoxia adaptation of A549 tumor cells. The survival and invasion capacity of the tumor cells under hypoxia was suppressed by T3E via the inactivation of Src. More specifically, T3E-dependent inhibition of Src-induced Akt activation contributed to suppression of cell survival under hypoxia, and the reduction of fibrinolytic factors such as plasminogen activator-1(PAI-1) via the decrease of hypoxia-inducible factor-2alpha by T3E led to inhibition of hypoxic invasion. Overall these results suggest that T3E suppresses hypoxia adaptation of A549 cells by the inhibition in hypoxia-induced activation of Src signaling.
巻・号 365(4)
ページ 875-81
公開日 2008-1-25
DOI 10.1016/j.bbrc.2007.11.085
PII S0006-291X(07)02508-9
PMID 18042466
MeSH Adaptation, Physiological / drug effects Cell Hypoxia / drug effects Cell Line, Tumor Cell Survival / drug effects* Humans Lung Neoplasms / metabolism* Lung Neoplasms / pathology* Oxidation-Reduction / drug effects Oxygen / metabolism* Tocotrienols / administration & dosage*
IF 2.985
引用数 25
WOS 分野 BIOPHYSICS BIOCHEMISTRY & MOLECULAR BIOLOGY
リソース情報
ヒト・動物細胞