Zhang Jian, Xu Yong-Jian, Xiong Wei-Ning, Zhang Zhen-Xiang, DU Chun-Ling, Qiao Li-Fen, Ni Wang, Chen Shi-Xin
Department of Respiratory Medicine, Tongji Hospital, Tongji Medical School, Huazhong University of Science and Technology,Wuhan, Hubei, 430030, P R China.
Ai Zheng. 2008 Jul;27(7):710-5.
BACKGROUND & OBJECTIVE: Recent studies have shown that activation of nuclear factor-kappaB(NF-kappaB) can regulate the invasion and metastasis of cancer cells. The present study was to investigate inhibition of NF-kappaB activity on invasion of human lung cancer cell line A549 and the possible mechanism.
The recombinant plasmid pcDNA3.1(+)/IkappaBalpha, expressing the alpha isoform (IkappaBalpha) of the NF-kappaB inhibitor, was constructed. A549 cells were cultured in vitro and divided into non-transfection group, pcDNA3.1(+) transfected group and pcDNA3.1(+)/IkappaBalpha transfected group. The expression of IkappaBalpha was detected by reverse transcription-polymerase chain reaction (RT-PCR) and Western blotting. The activity of NF-kappaB was determined by electrophoretic mobility shift assay (EMSA). Invasion of A549 cells was assessed by transwell chamber assay. The expression of MMP-2 and MMP-9 was detected by RT-PCR and gelatin zymography.
Plasmid pcDNA3.1(+)/IkappaBalpha was successfully constructed and expressed in A549 cells. The activity of NF-kappaB, the number of invasive cells, the activity of MMP-2 and MMP-9 of A549 cells in pcDNA3.1(+)/IkappaBalpha transfected group were significantly lower than those in non-transfection group and pcDNA3.1(+) transfected group (all P<0.05).
Transfection of IkappaBalpha can inhibit NF-kappaB activity, thus inhibit cell invasion of A549, which may be through the down-regulation of MMP-2 and MMP-9 expressions.
近期研究表明,核因子-κB(NF-κB)的激活可调节癌细胞的侵袭和转移。本研究旨在探讨抑制NF-κB活性对人肺癌细胞系A549侵袭的影响及其可能机制。
构建表达NF-κB抑制剂α亚型(IkappaBalpha)的重组质粒pcDNA3.1(+)/IkappaBalpha。体外培养A549细胞,分为未转染组、pcDNA3.1(+)转染组和pcDNA3.1(+)/IkappaBalpha转染组。采用逆转录-聚合酶链反应(RT-PCR)和蛋白质印迹法检测IkappaBalpha的表达。采用电泳迁移率变动分析(EMSA)测定NF-κB的活性。采用Transwell小室分析法评估A549细胞的侵袭能力。采用RT-PCR和明胶酶谱法检测基质金属蛋白酶-2(MMP-2)和基质金属蛋白酶-9(MMP-9)的表达。
成功构建质粒pcDNA3.1(+)/IkappaBalpha并在A549细胞中表达。pcDNA3.1(+)/IkappaBalpha转染组A549细胞的NF-κB活性、侵袭细胞数、MMP-2和MMP-9活性均显著低于未转染组和pcDNA3.1(+)转染组(均P<0.05)。
转染IkappaBalpha可抑制NF-κB活性,从而抑制A549细胞的侵袭,其机制可能是通过下调MMP-2和MMP-9的表达。