RRC ID |
43184
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著者 |
Kashiwagi K, Harada K, Yano Y, Kumadaki I, Hagiwara K, Takebayashi J, Kido W, Virgona N, Yano T.
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タイトル |
A redox-silent analogue of tocotrienol inhibits hypoxic adaptation of lung cancer cells.
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ジャーナル |
Biochem Biophys Res Commun
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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.
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巻・号 |
365(4)
|
ページ |
875-81
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公開日 |
2008-1-25
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DOI |
10.1016/j.bbrc.2007.11.085
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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
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リソース情報 |
ヒト・動物細胞 |
|