2008Experimental PathologyRequires access

Expression of COX-2 and its relationship to angiogenesis in human brain gliomas

WU Jian-liang

Open publisher page 0 citations

Abstract

Purpose To detect the expression of cyclooxygenase-2(COX-2),vascular endothelial growth factor(VEGF) and CD34 in surgically removed human gliomas and to study the relationship and significance among COX-2,VEGF,micro vessels density(MVD) and angiogenesis in gliomas.Methods Immunohistochemical SP method was used to investigate the expression of COX-2,VEGF and CD34 among 80 human glioma samples and 10 normal brain tissue samples respectively.Results Positive cells of COX-2 and VEGF were distributed in the area close to necrosis and in the area with intensive blood vessels.The positive rates of COX-2 and VEGF in 80 glioma samples were 68.8% and 72.5% and there was no expression in normal brain tissue.The expression of COX-2 and VEGF was associated with MVD(r=0.927,r=0.939,P0.05);the expression of COX-2 was associated with VEGF(r=0.885,P0.05);the pathologic grade of gliomas was associated with COX-2,VEGF and MVD(r=0.894,r=0.927,r=0.865,P0.05).Conclusion COX-2 and VEGF play an important role in the glioma growing and progressing and are closely associated with malignancy.COX-2 may accelerate the tumor's angiogenesis through up-regulating the expression of VEGF.

About this research paper

What this paper is about

Purpose To detect the expression of cyclooxygenase-2(COX-2),vascular endothelial growth factor(VEGF) and CD34 in surgically removed human gliomas and to study the relationship and significance among COX-2,VEGF,micro vessels density(MVD) and angiogenesis in gliomas.Methods Immunohistochemical SP method was used to investigate the expression of COX-2,VEGF and CD34 among 80 human glioma samples and 10 normal brain tissue samples respectively.Results Positive cells of COX-2 and VEGF were distributed in the area close to necrosis and in the area with intensive blood vessels.The positive rates of COX-2 and VEGF in 80 glioma samples were 68.8% and 72.5% and there was no expression in normal brain tissue.The expression of COX-2 and VEGF was associated with MVD(r=0.927,r=0.939,P0.05);the expression of COX-2 was associated with VEGF(r=0.885,P0.05);the pathologic grade of gliomas was associated with COX-2,VEGF and MVD(r=0.894,r=0.927,r=0.865,P0.05).Conclusion COX-2 and VEGF play an important role in the glioma growing and progressing and are closely associated with malignancy.COX-2 may accelerate the tumor's angiogenesis through up-regulating the expression of VEGF.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Purpose To detect the expression of cyclooxygenase-2(COX-2),vascular endothelial growth factor(VEGF) and CD34 in surgically removed human gliomas and to study the relationship and significance among COX-2,VEGF,micro vessels density(MVD) and angiogenesis in gliomas.Methods Immunohistochemical SP method was used to investigate the expression of COX-2,VEGF and CD34 among 80 human glioma samples and 10 normal brain tissue samples respectively.Results Positive cells of COX-2 and VEGF were distributed in the area close to necrosis and in the area with intensive blood vessels.The positive rates of COX-2 and VEGF in 80 glioma samples were 68.8% and 72.5% and there was no expression in normal brain tissue.The expression of COX-2 and VEGF was associated with MVD(r=0.927,r=0.939,P0.05);the expression of COX-2 was associated with VEGF(r=0.885,P0.05);the pathologic grade of gliomas was associated with COX-2,VEGF and MVD(r=0.894,r=0.927,r=0.865,P0.05).Conclusion COX-2 and VEGF play an important role in the glioma growing and progressing and are closely associated with malignancy.COX-2 may accelerate the tumor's angiogenesis through up-regulating the expression of VEGF.

Key concepts: Angiogenesis, Glioma, CD34, Immunohistochemistry, Pathology, Malignancy, Vascular endothelial growth factor, VEGF receptors

Related papers

Back to paper searchBrowse research topicsOriginal source
Expression of COX-2 and its relationship to angiogenesis in human brain gliomas — Research Paper | ScholarLens