Limitations of the reporter green fluorescent protein under simulated tumor conditions

被引:1
|
作者
Coralli, C [1 ]
Cemazar, M [1 ]
Kanthou, C [1 ]
Tozer, GM [1 ]
Dachs, GU [1 ]
机构
[1] Mt Vernon Hosp, Canc Res Trust, Gray Lab, Tumor Microcirculat Lab, Northwood HA6 2JR, Middx, England
关键词
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This paper reports a detailed analysis of the effect of low oxygen conditions (hypoxia) on the reporter green fluorescent protein (GFP). It questions the feasibility of using GFP fur gene expression studies under tumor conditions. Hypoxia is a characteristic of both experimental and clinical tumors. Several important factors are pointed out which need to be considered when using GFP as reporter gene. GFP fluorescence is the final product of a long and complex pathway involving transcription, translation, and posttranslational modifications. All of these steps may be affected by the availability of oxygen. We show specifically that cellular GFPfluorescence decreased with reduced oxygenation, anoxia virtually eliminated fluorescence and protein levels, and fluorescence recovery after anoxia required 5-10 h of reoxygenation, In conclusion, GFP appears to be a good marker gene to study location or movement of proteins or cells but should he used with great caution as a reporter of gene expression under tumor renditions.
引用
收藏
页码:4784 / 4790
页数:7
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