Special issue: Sepsis Gene expression profiling in sepsis: timing, tissue, and translational considerations

被引:101
作者
Maslove, David M. [1 ,2 ]
Wong, Hector R. [3 ,4 ,5 ]
机构
[1] St Michaels Hosp, Li Ka Shing Knowledge Inst, Toronto, ON M5B 1W8, Canada
[2] Univ Toronto, Dept Med, Toronto, ON, Canada
[3] Cincinnati Childrens Hosp, Med Ctr, Div Crit Care Med, Cincinnati, OH 45229 USA
[4] Cincinnati Childrens Res Fdn, Cincinnati, OH USA
[5] Univ Cincinnati, Coll Med, Dept Pediat, Cincinnati, OH USA
关键词
sepsis; septic shock; gene expression; microarrays; genomics; bioinformatics; MATRIX METALLOPROTEINASES; DIAGNOSTIC BIOMARKER; BACTERIAL-INFECTION; ENDOTOXIN CHALLENGE; PEDIATRIC SEPSIS; BLOOD LEUKOCYTES; DOUBLE-BLIND; WHOLE-BLOOD; ZINC; TIME;
D O I
10.1016/j.molmed.2014.01.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Sepsis is a complex inflammatory response to infection. Microarray-based gene expression studies of sepsis have illuminated the complex pathogen recognition and inflammatory signaling pathways that characterize sepsis. More recently, gene expression profiling has been used to identify diagnostic and prognostic gene signatures, as well as novel therapeutic targets. Studies in pediatric cohorts suggest that transcriptionally distinct subclasses might account for some of the heterogeneity seen in sepsis. Time series analyses have pointed to rapid and dynamic shifts in transcription patterns associated with various phases of sepsis. These findings highlight current challenges in sepsis knowledge translation, including the need to adapt complex and time-consuming whole-genome methods for use in the intensive care unit environment, where rapid diagnosis and treatment are essential.
引用
收藏
页码:204 / 213
页数:10
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