Article

Transcription expression and clinical significance of vascular endothelial growth factor mRNA and endostatin mRNA in pleural effusions of patients with lung cancer.

Department of Pathology, The First Affiliated Hospital and College of Basic Medical Sciences, China Medical University, Shenyang, China.
Diagnostic Cytopathology (impact factor: 1.16). 04/2012; 40(4):287-91. DOI:10.1002/dc.21546 pp.287-91
Source: PubMed

ABSTRACT The aim of this study was to evaluate the individual and combined diagnostic utility of vascular endothelial growth factor (VEGF) mRNA and endostatin mRNA in pleural effusions of patients with lung cancer. Transcription levels of VEGF and endostatin were detected by reverse transcription polymerase chain reaction (RT-PCR) in pleural effusions of patients with lung cancer (92 cases) and with lung benign disease (36 cases). Both VEGF mRNA and endostatin mRNA was significantly higher in malignant, AC, and SCC effusions than in benign effusions (P < 0.01). In the subgrouping, VEGF mRNA was obviously higher than endostatin mRNA in malignant and AC effusions (P < 0.01), whereas VEGF mRNA and endostatin mRNA did not differ between AC group and SCC group (P > 0.05). In single, VEGF mRNA had the highest sensitivity (82.6%) and accuracy (84.3%), whereas endostatin mRNA had the highest specificity (100%). When combinations of VEGF mRNA and endostatin mRNA were evaluated together, they gave a high-diagnostic performance: sensitivity of 95.7% and accuracy of 93.8%, respectively. The detection of VEGF mRNA and endostatin mRNA appears to be suitable for distinguishing carcinoma cells from reactive mesothelial cells in pleural effusions, they could be useful to diagnose the pleural micrometastasis.

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Keywords

AC effusions
 
AC group
 
benign effusions
 
diagnostic utility
 
distinguishing carcinoma cells
 
endostatin mRNA
 
high-diagnostic performance
 
highest sensitivity
 
highest specificity
 
lung benign disease
 
lung cancer
 
patients
 
pleural effusions
 
pleural micrometastasis
 
reactive mesothelial cells
 
reverse transcription polymerase chain reaction
 
SCC effusions
 
SCC group
 
vascular endothelial growth factor
 
VEGF mRNA
 

Ying Chen