Zhou Yongan, Wang Yafang, Zhao Zhengwei, Wang Yanxia, Zhang Ning, Zhang Helong, Liu Lili
1 Department of Thoracic Surgery, Tangdu Hospital, The Fourth Military Medical University, Xi'an, China.
2 Department of Oncology, Tangdu Hospital, The Fourth Military Medical University, Xi'an, China.
Tumour Biol. 2017 Jun;39(6):1010428317701655. doi: 10.1177/1010428317701655.
We previously reported that 37-kDa laminin receptor precursor involved in metastasis of lung adenocarcinoma cancer cells. In this study, we further revealed that hypoxia induced 37-kDa laminin receptor precursor expression and activation of extracellular signal-regulated protein kinase, c-Jun N-terminal kinase, and p38 mitogen-activated protein kinase in lung adenocarcinoma cancer cells. In addition, we further demonstrated that the c-Jun N-terminal kinase inhibitor SP600125 and extracellular signal-regulated protein kinase inhibitor U0126 blocked the c-Jun activity and abolished hypoxia-induced 37-kDa laminin receptor precursor expression and promoter activity in a concentration-dependent manner. However, the p38 mitogen-activated protein kinase inhibitor did not affect 37-kDa laminin receptor precursor expression and c-Jun activity in response to hypoxia. Furthermore, downregulated c-Jun expression by short interfering RNA could also inhibit hypoxia-induced 37-kDa laminin receptor precursor expression and transcriptional activity. The inhibition of 37-kDa laminin receptor precursor expression by SP600125 and U0126 could be rescued by c-Jun overexpression. Studies using luciferase promoter constructs revealed a significant increase in the activity of promoter binding in the cells exposed to hypoxia, which was lost in the cells with mutation of the activator protein 1 binding site. Electrophoresis mobility shift assay and chromatin immunoprecipitation demonstrated a functional activator protein 1 binding site within 37-kDa laminin receptor precursor gene regulatory sequence located at -271 relative to the transcriptional initiation point. Hypoxia-induced invasion of A549 cells was inhibited by the pharmacologic inhibitors of c-Jun N-terminal kinase (SP600125) and extracellular signal-regulated protein kinase (U0126) as well as 37-kDa laminin receptor precursor-specific siRNA or antibody. Our results suggest that hypoxia-elicited c-Jun/activator protein 1 regulates 37-kDa laminin receptor precursor expression, which modulates migration and invasion of lung adenocarcinoma cells.
我们之前报道过,37 kDa层粘连蛋白受体前体参与肺腺癌细胞的转移。在本研究中,我们进一步揭示,缺氧诱导肺腺癌细胞中37 kDa层粘连蛋白受体前体的表达以及细胞外信号调节蛋白激酶、c-Jun氨基末端激酶和p38丝裂原活化蛋白激酶的激活。此外,我们进一步证明,c-Jun氨基末端激酶抑制剂SP600125和细胞外信号调节蛋白激酶抑制剂U0126以浓度依赖的方式阻断c-Jun活性,并消除缺氧诱导的37 kDa层粘连蛋白受体前体的表达和启动子活性。然而,p38丝裂原活化蛋白激酶抑制剂并不影响缺氧条件下37 kDa层粘连蛋白受体前体的表达和c-Jun活性。此外,通过短发夹RNA下调c-Jun表达也可抑制缺氧诱导的37 kDa层粘连蛋白受体前体的表达和转录活性。SP600125和U0126对37 kDa层粘连蛋白受体前体表达的抑制作用可通过c-Jun过表达得以挽救。使用荧光素酶启动子构建体的研究表明,暴露于缺氧环境的细胞中启动子结合活性显著增加,而在激活蛋白1结合位点发生突变的细胞中这种活性丧失。电泳迁移率变动分析和染色质免疫沉淀表明,在相对于转录起始点位于-271的37 kDa层粘连蛋白受体前体基因调控序列内存在一个功能性激活蛋白1结合位点。c-Jun氨基末端激酶(SP600125)和细胞外信号调节蛋白激酶(U0126)的药理学抑制剂以及37 kDa层粘连蛋白受体前体特异性siRNA或抗体可抑制缺氧诱导的A549细胞侵袭。我们的结果表明,缺氧诱导的c-Jun/激活蛋白1调节37 kDa层粘连蛋白受体前体的表达,进而调节肺腺癌细胞的迁移和侵袭。