Vikhreva P N, Shepelev M V, Korobko I V
Institute of Gene Biology, Russian Academy of Sciences, 34/5 Vavilov str., Moscow 119334, Russia.
Institute of Gene Biology, Russian Academy of Sciences, 34/5 Vavilov str., Moscow 119334, Russia.
Biochim Biophys Acta. 2014 Jan;1839(1):43-9. doi: 10.1016/j.bbagrm.2013.12.001. Epub 2013 Dec 14.
Programmed cell death 4 (Pdcd4) tumor suppressor is frequently lost in tumors of various origins including lung cancer, and its loss contributes to tumor progression. However molecular mechanisms underlying Pdcd4 suppression in lung cancer cells remain largely unexplored. Here we investigated molecular mechanisms of Pdcd4 suppression in lung cancer cells. Besides enhanced mTOR-dependent proteasomal degradation of Pdcd4 protein, we found that Pdcd4 transcription is negatively regulated by mTOR signaling, and localized cis-acting element in Pdcd4 promoter responsible for this effect. In conclusion, we described a novel molecular mechanism of Pdcd4 suppression in cancer cells consisting from mTOR signaling-dependent transcriptional repression of Pdcd4.
程序性细胞死亡4(Pdcd4)肿瘤抑制因子在包括肺癌在内的各种起源的肿瘤中经常缺失,其缺失促进肿瘤进展。然而,肺癌细胞中Pdcd4抑制的分子机制在很大程度上仍未被探索。在此,我们研究了肺癌细胞中Pdcd4抑制的分子机制。除了增强mTOR依赖的Pdcd4蛋白的蛋白酶体降解外,我们发现Pdcd4转录受到mTOR信号的负调控,并且Pdcd4启动子中负责这种效应的顺式作用元件位于局部。总之,我们描述了一种癌细胞中Pdcd4抑制的新分子机制,该机制由mTOR信号依赖的Pdcd4转录抑制组成。