Neil Jason R, Schiemann William P
Department of Pharmacology, University of Colorado Health Sciences Center, Aurora, CO 80045, USA.
Cancer Res. 2008 Mar 1;68(5):1462-70. doi: 10.1158/0008-5472.CAN-07-3094.
The conversion of transforming growth factor beta (TGF-beta) from a tumor suppressor to a tumor promoter occurs frequently during mammary tumorigenesis, yet the molecular mechanisms underlying this phenomenon remain undefined. We show herein that TGF-beta repressed nuclear factor-kappaB (NF-kappaB) activity in normal NMuMG cells, but activated this transcription factor in their malignant counterparts, 4T1 cells, by inducing assembly of TGF-beta-activated kinase 1 (TAK1)-binding protein 1 (TAB1):I kappaB kinase beta (IKK beta) complexes, which led to the stimulation of a TAK1:IKK beta:p65 pathway. TAB1:IKK beta complexes could only be detected in NMuMG cells following their induction of epithelial-mesenchymal transition (EMT), which, on TGF-beta treatment, activated NF-kappaB. Expression of a truncated TAB1 mutant [i.e., TAB1(411)] reduced basal and TGF-beta-mediated NF-kappaB activation in NMuMG cells driven to undergo EMT by TGF-beta and in 4T1 cells stimulated by TGF-beta. TAB1(411) expression also inhibited TGF-beta-stimulated tumor necrosis factor-alpha and cyclooxygenase-2 expression in 4T1 cells. Additionally, the ability of human MCF10A-CA1a breast cancer cells to undergo invasion in response to TGF-beta absolutely required the activities of TAK1 and NF-kappaB. Moreover, small interfering RNA-mediated TAK1 deficiency restored the cytostatic activity of TGF-beta in MCF10A-CA1a cells. Finally, expression of truncated TAB1(411) dramatically reduced the growth of 4T1 breast cancers in syngeneic BALB/c, as well as in nude mice, suggesting a potentially important role of NF-kappaB in regulating innate immunity by TGF-beta. Collectively, our findings have defined a novel TAB1:TAK1:IKK beta:NF-kappaB signaling axis that forms aberrantly in breast cancer cells and, consequently, enables oncogenic signaling by TGF-beta.
在乳腺肿瘤发生过程中,转化生长因子β(TGF-β)从肿瘤抑制因子转变为肿瘤促进因子的情况频繁发生,然而这一现象背后的分子机制仍不明确。我们在此表明,TGF-β在正常的NMuMG细胞中抑制核因子-κB(NF-κB)活性,但在其恶性对应物4T1细胞中激活该转录因子,这是通过诱导TGF-β激活激酶1(TAK1)结合蛋白1(TAB1):IκB激酶β(IKKβ)复合物的组装实现的,进而导致TAK1:IKKβ:p65信号通路的激活。只有在NMuMG细胞诱导上皮-间质转化(EMT)后才能检测到TAB1:IKKβ复合物,在TGF-β处理后,该复合物会激活NF-κB。截短的TAB1突变体[即TAB1(411)]的表达降低了在TGF-β驱动下经历EMT的NMuMG细胞以及TGF-β刺激的4T1细胞中的基础和TGF-β介导的NF-κB激活。TAB1(411)的表达也抑制了TGF-β刺激的4T1细胞中肿瘤坏死因子-α和环氧合酶-2的表达。此外,人MCF10A-CA1a乳腺癌细胞响应TGF-β进行侵袭的能力绝对需要TAK1和NF-κB的活性。而且,小干扰RNA介导的TAK1缺陷恢复了TGF-β在MCF10A-CA1a细胞中的细胞生长抑制活性。最后,截短的TAB1(411)的表达显著降低了同基因BALB/c小鼠以及裸鼠中4T1乳腺癌肿瘤的生长,这表明NF-κB在TGF-β调节固有免疫中可能具有重要作用。总体而言,我们的研究结果确定了一种新的TAB1:TAK1:IKKβ:NF-κB信号轴,该信号轴在乳腺癌细胞中异常形成,从而使TGF-β能够进行致癌信号传导。