RNA interference targeting raptor inhibits proliferation of gastric cancer cells

Mammalian target of rapamycin complex 1 (mTORC1) is dysregulated in gastric cancer. The biologic function of mTORC1 in gastric carcinogenesis is unclear. Here, we demonstrate that disruption of mTORC1 function by RNA interference-mediated downregulation of raptor substantially inhibited gastric canc...

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Veröffentlicht in:Experimental cell research 2011-06, Vol.317 (10), p.1353-1358
Hauptverfasser: Wu, William Ka Kei, Lee, Chung Wa, Cho, Chi Hin, Chan, Francis Ka Leung, Yu, Jun, Sung, Joseph Jao Yiu
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Sprache:eng
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Zusammenfassung:Mammalian target of rapamycin complex 1 (mTORC1) is dysregulated in gastric cancer. The biologic function of mTORC1 in gastric carcinogenesis is unclear. Here, we demonstrate that disruption of mTORC1 function by RNA interference-mediated downregulation of raptor substantially inhibited gastric cancer cell proliferation through induction of G 0/G 1-phase cell cycle arrest. The anti-proliferative effect was accompanied by concomitant downregulation of activator protein-1 and upregulation of Smad2/3 transcriptional activities. In addition, the expression of cyclin D 3 and p21 Waf1, which stabilizes cyclin D/cdk4 complex for G 1–S transition, was reduced by raptor knockdown. In conclusion, disruption of mTORC1 inhibits gastric cancer cell proliferation through multiple pathways. This discovery may have an implication in the application of mTORC1-directed therapy for the treatment of gastric cancer.
ISSN:0014-4827
1090-2422
DOI:10.1016/j.yexcr.2011.03.005