MicroRNA-203 leads to G1 phase cell cycle arrest in laryngeal carcinoma cells by directly targeting survivin

► Overexpression of miR-203 inhibits laryngeal cancer cell proliferation. ► Survivin is a direct target of miR-203 in laryngeal cancer cells. ► Survivin plays a critical role in miR-203-induced G1 phase cell cycle arrest. ► Survivin mRNA inversely correlates with miR-203 in human laryngeal carcinoma...

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Veröffentlicht in:FEBS letters 2012-03, Vol.586 (6), p.804-809
Hauptverfasser: Bian, Ka, Fan, Jing, Zhang, Xiang, Yang, Xin-Wei, Zhu, Hua-Yu, Wang, Lei, Sun, Jian-Yong, Meng, Yan-Ling, Cui, Peng-Cheng, Cheng, Shi-Yin, Zhang, Jian, Zhao, Jing, Yang, An-Gang, Zhang, Rui
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Sprache:eng
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Zusammenfassung:► Overexpression of miR-203 inhibits laryngeal cancer cell proliferation. ► Survivin is a direct target of miR-203 in laryngeal cancer cells. ► Survivin plays a critical role in miR-203-induced G1 phase cell cycle arrest. ► Survivin mRNA inversely correlates with miR-203 in human laryngeal carcinoma. Previous studies have shown that miR-203 acts as a tumor-suppressive microRNA in various cancers, but its roles in laryngeal carcinoma are still contradicted. Here, we found that miR-203 inhibited the growth of laryngeal cancer cells and survivin was a direct target of miR-203. Moreover, silencing of survivin recapitulated the effect of miR-203 on cell cycle progression, whereas overexpression of survivin reversed this effect. Additionally, qRT-PCR showed the reciprocal relationship between miR-203 and survivin in laryngeal cancer tissues. These findings indicate that miR-203 inhibits the proliferation of laryngeal carcinoma cells by directly targeting survivin, suggesting its application in anti-cancer therapeutics.
ISSN:0014-5793
1873-3468
DOI:10.1016/j.febslet.2012.01.050