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永生化正常人支气管上皮细胞系和非小细胞肺癌细胞系中的组成型和诱导型核因子-κB

Constitutive and inducible nuclear factor-kappaB in immortalized normal human bronchial epithelial and non-small cell lung cancer cell lines.

作者信息

Baby Johnson, Pickering Brian F, Vashisht Gopal Y N, Van Dyke Michael W

机构信息

Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030-4009, USA.

出版信息

Cancer Lett. 2007 Sep 18;255(1):85-94. doi: 10.1016/j.canlet.2007.03.024. Epub 2007 May 9.

Abstract

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.

摘要

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。

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