Effect of Danggui Buxue Decoction on Proliferation and its Molecular Mechanism in Tumor Vascular Endothelial Cells
|更新时间:2024-01-04
|
Effect of Danggui Buxue Decoction on Proliferation and its Molecular Mechanism in Tumor Vascular Endothelial Cells
Chinese Journal of Experimental Traditional Medical FormulaeVol. 19, Issue 2, Pages: 163-167(2013)
作者机构:
作者简介:
基金信息:
DOI:
CLC:
Published:2013
稿件说明:
移动端阅览
ZHANG San-yin, FENG Pei, YANG Miao. Effect of Danggui Buxue Decoction on Proliferation and its Molecular Mechanism in Tumor Vascular Endothelial Cells[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(2): 163-167.
DOI:
ZHANG San-yin, FENG Pei, YANG Miao. Effect of Danggui Buxue Decoction on Proliferation and its Molecular Mechanism in Tumor Vascular Endothelial Cells[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(2): 163-167.DOI:
Effect of Danggui Buxue Decoction on Proliferation and its Molecular Mechanism in Tumor Vascular Endothelial Cells
Objective: To study the effect of Danggui Buxue decoction(DBD) on proliferation in tumor vascular endothelial cells
and to explore the mechanism of inhibition of tumor angiogenesis. Method: After different doses of DBD acting on vascular endothelial cells (EA. Hy926) co-cultured with the tumor cells (A549) model
CCK-8 assay was used to observe the proliferation of vascular endothelial cells co-cultured with the tumor cells; enzyme-cinked immunosorbant assay (ELISA) was used for assay of vascular endothelia growth factor (VEGF) and its receptors (VEGFR1
VEGFR2
sVEGFR1
sVEGFR2) and expression of vascular endothelial cells co-cultured with the tumor cells. Result: Compared with normal group
vascular endothelial cells co-cultured with tumor cells proliferation capacity increased (P<0.01); DBD each dose group could promote the proliferation of normal endothelial cells
inhibit the proliferation of vascular endothelial cells co-cultured with tumor cells with a manner of dose and effect
compared with model group
there was significant difference (P<0.01). DBD each dose could promote vascular endothelial cell co-cultured with tumor cells expression of VEGF
compared with model group
co-cultured of high dose group and dose group showed a significantly different (P<0.01). Co-culture model group was significantly up-regulate VEGFR1
VEGFR2 expression
the groups DBD inhibited the expression of VEGFR1
VEGFR2 and showed a dose relationship. Co-cultured with tumor vascular endothelial cells in model group decreased expression of sVEGFR1 and sVEGFR2
each dose group of DBD could promote sVEGFR1 and sVEGFR2 expression
showed a dose relationship. Conclusion: DBD can Inhibit proliferation of vascular endothelial cells co-cultured with the tumor cells. The mechanism might be related to regulation of VEGF and its receptors