ATRA-inhibited proliferation in glioma cells is associated with subcellular redistribution of β-catenin via up-regulation of Axin

Retinoic acid (RA) is a major chemopreventive agent which exerts strong anti-tumor activity partly by trans-repressing the Wnt/β-catenin signaling pathway in some tumor cell lines. However, the definite mechanism of RA trans-repression of the Wnt/β-catenin signaling pathway has not been elucidated c...

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Veröffentlicht in:Journal of neuro-oncology 2008-05, Vol.87 (3), p.271-277
Hauptverfasser: Lu, Jianrong, Zhang, Feng, Zhao, Daqing, Hong, Liu, Min, Jie, Zhang, Liying, Li, Fanfan, Yan, Yan, Li, Hang, Ma, Yu, Li, Qing
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Sprache:eng
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Zusammenfassung:Retinoic acid (RA) is a major chemopreventive agent which exerts strong anti-tumor activity partly by trans-repressing the Wnt/β-catenin signaling pathway in some tumor cell lines. However, the definite mechanism of RA trans-repression of the Wnt/β-catenin signaling pathway has not been elucidated clearly. In this work, we found that all-trans retinoic acid (ATRA) significantly inhibited proliferation of glioma cells, accompanied by up-regulation of expression of Axin and altered subcellular distribution of β-catenin. Transfecting C6 cells with rAxin further confirmed that increased expression of Axin is obligate for inhibition of proliferation and the increase of the cytoplasmic β-catenin. Our results suggested that Axin might play an important role in RA-mediated anti-proliferative effects of glioma cell lines.
ISSN:0167-594X
1573-7373
DOI:10.1007/s11060-008-9518-4