Wang Feng, Xu Ping, Xie Kuang-Chen, Chen Xia-Fang, Li Chuan-Yuan, Huang Qian
Experimental Research Center, The First People's Hospital, Shanghai Jiaotong University, Shanghai 200080, P.R. China ;
Department of Radiation Oncology, University of Colorado Health Sciences Center, Aurora, CO 80010, USA.
Biomed Rep. 2013 Jul;1(4):539-544. doi: 10.3892/br.2013.115. Epub 2013 May 28.
The expression of vascular endothelial growth factor (VEGF) is regulated by microenvironmental factors within the tumors, such as hypoxia, free radicals, pH imbalance and nutrient deficiency. The purpose of this study was to observe VEGF activity in tumor cells under different stress conditions. A plasmid was generated, consisting of green fluorescent protein (GFP) fused to a 1,217-bp sequence, which was located downstream and upstream of the transcriptional start site of VEGF, respectively. The plasmid was stably transfected into 4T1 mouse breast carcinoma cells. Cells were cultured in a medium with nitric oxide (NO) donor sodium nitroprusside (SNP), hypoxia-mimetic agent deferoxamine mesylate (DFX), HO, absence of serum and lowered or elevated pH, or were heat-shocked, followed by measurement of VEGF activity by reverse transcription polymerase chain reaction (RT-PCR) and ELISA. Hypoxia, SNP and HO led to increments of VEGF mRNA and protein expression, as well as of GFP expression. The pH alterations, serum deprivation and heat shock reduced VEGF mRNA expression, but had little effect on GFP expression. The results demonstrated that VEGF expression may be influenced by a number of microenvironmental factors and these factors may play important roles in regulating VEGF expression during tumorigenesis.
血管内皮生长因子(VEGF)的表达受肿瘤内微环境因素的调控,如缺氧、自由基、pH失衡和营养缺乏。本研究的目的是观察不同应激条件下肿瘤细胞中VEGF的活性。构建了一个质粒,其由绿色荧光蛋白(GFP)与一个1217bp的序列融合而成,该序列分别位于VEGF转录起始位点的下游和上游。将该质粒稳定转染至4T1小鼠乳腺癌细胞中。细胞在含有一氧化氮(NO)供体硝普钠(SNP)、缺氧模拟剂甲磺酸去铁胺(DFX)、HO、无血清以及pH降低或升高的培养基中培养,或进行热休克处理,随后通过逆转录聚合酶链反应(RT-PCR)和酶联免疫吸附测定(ELISA)测量VEGF活性。缺氧、SNP和HO导致VEGF mRNA和蛋白表达以及GFP表达增加。pH改变、血清剥夺和热休克降低了VEGF mRNA表达,但对GFP表达影响较小。结果表明,VEGF表达可能受多种微环境因素影响,这些因素可能在肿瘤发生过程中调节VEGF表达方面发挥重要作用。