Department of Cancer Biology, University of Texas MD Anderson Cancer Center, Houston, Texas 77030, USA.
Cancer Res. 2010 May 15;70(10):4054-63. doi: 10.1158/0008-5472.CAN-09-2110. Epub 2010 May 4.
Human enhancer of filamentation 1 (HEF1; also known as NEDD9 or Cas-L) is a scaffolding protein that is implicated in regulating diverse cellular processes, such as cellular attachment, motility, cell cycle progression, apoptosis, and inflammation. Here, we identify HEF1 as a novel hypoxia-inducible factor-1alpha (HIF-1alpha)-regulated gene and reveal that HEF1 mediates hypoxia-induced migration of colorectal carcinoma cells. HEF1 is highly expressed in cultured colorectal carcinoma cells exposed to hypoxia and in the hypoxic areas of human colorectal cancer (CRC) specimens. Moreover, our data show that HIF-1alpha mediates the effects of hypoxia on induction of HEF1 expression via binding to a hypoxia-responsive element of the HEF1 promoter. Importantly, the induction of HEF1 expression significantly enhances hypoxia-stimulated HIF-1alpha transcriptional activity by modulating the interaction between HIF-1alpha and its transcriptional cofactor p300. Inhibition of HEF1 expression also reduced the levels of hypoxia-inducible genes, including those that regulate cell motility. Cell migration was reduced dramatically following knockdown of HEF1 expression under hypoxic conditions. Thus, this positive feedback loop may contribute to adaptive responses of carcinoma cells encountering hypoxia during cancer progression.
人丝氨酸/苏氨酸蛋白激酶 1 增强子(HEF1;也称为 NEDD9 或 Cas-L)是一种支架蛋白,涉及调节多种细胞过程,如细胞附着、运动、细胞周期进程、细胞凋亡和炎症。在这里,我们确定 HEF1 是一种新的缺氧诱导因子-1α(HIF-1α)调节基因,并揭示 HEF1 介导结直肠癌细胞的缺氧诱导迁移。HEF1 在培养的结直肠癌细胞暴露于缺氧和人类结直肠癌(CRC)标本的缺氧区域中高度表达。此外,我们的数据表明,HIF-1α 通过与 HEF1 启动子的缺氧反应元件结合来介导缺氧对 HEF1 表达的诱导作用。重要的是,HEF1 表达的诱导通过调节 HIF-1α 与其转录共激活因子 p300 之间的相互作用,显著增强了缺氧刺激的 HIF-1α 转录活性。抑制 HEF1 表达也降低了缺氧诱导基因的水平,包括调节细胞运动的基因。在缺氧条件下敲低 HEF1 表达后,细胞迁移明显减少。因此,这个正反馈回路可能有助于癌细胞在癌症进展过程中遇到缺氧时的适应性反应。