Baby Johnson, Pickering Brian F, Vashisht Gopal Y N, Van Dyke Michael W
Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030-4009, USA.
Cancer Lett. 2007 Sep 18;255(1):85-94. doi: 10.1016/j.canlet.2007.03.024. Epub 2007 May 9.
Constitutive activation of the proinflammatory nuclear factor kappaB (NF-kappaB) transcription factor p65(RelA)/p50 has been implicated in many cancers, including leukemias, lymphomas, and several solid tumors, including lung cancer. In many cases, constitutive NF-kappaB activation can be recapitulated in cell lines isolated from these cancers. To test whether this is the case with non-small cell lung cancer (NSCLC) cell lines, we investigated the basal levels of NF-kappaB proteins, their subcellular distribution, their DNA-binding activities, and the expression of NF-kappaB-responsive genes in 10 NSCLC cell lines. The immortalized human bronchial epithelial cell line BEAS-2B served as a normal control. We found little evidence of substantial constitutive NF-kappaB activation in NSCLC cell lines, although most all of the normal and NSCLC cells possessed inducible NF-kappaB. Our findings provide a resource for the use of particular NSCLC cell lines for the investigation of constitutive and inducible NF-kappaB activity in vitro.
促炎核因子κB(NF-κB)转录因子p65(RelA)/p50的组成性激活与许多癌症有关,包括白血病、淋巴瘤以及几种实体瘤,如肺癌。在许多情况下,从这些癌症中分离出的细胞系中可重现组成性NF-κB激活。为了测试非小细胞肺癌(NSCLC)细胞系是否也是这种情况,我们研究了10种NSCLC细胞系中NF-κB蛋白的基础水平、其亚细胞分布、其DNA结合活性以及NF-κB反应性基因的表达。永生化的人支气管上皮细胞系BEAS-2B用作正常对照。我们几乎没有发现NSCLC细胞系中存在大量组成性NF-κB激活的证据,尽管几乎所有正常细胞和NSCLC细胞都具有可诱导的NF-κB。我们的研究结果为利用特定的NSCLC细胞系在体外研究组成性和可诱导性NF-κB活性提供了资源。