LIU Zhi-gang,CHEN Fang-yu,JIANG Li-hui,WANG Tao.Angiostatin down-regulates vascular endothelial growth factor expression in human tongue squamous cell carcinoma cells[J].J Amry Med Univ (J Third Mil Med Univ),2008,30(16):1557-1560.
LIU Zhi-gang,CHEN Fang-yu,JIANG Li-hui,WANG Tao.Angiostatin down-regulates vascular endothelial growth factor expression in human tongue squamous cell carcinoma cells[J].J Amry Med Univ (J Third Mil Med Univ),2008,30(16):1557-1560.DOI:
Angiostatin down-regulates vascular endothelial growth factor expression in human tongue squamous cell carcinoma cells
Objective To evaluate the effects of angiostatin on vascular endothelial growth factor expression in human tongue squamous cell carcinoma cells. Methods Subcutaneous xenografts of human tongue squamous cell carcinoma (Tca8113) cell line in BALB/c nude mice were employed and eighteen mice were randomly divided into three groups (6 mice each): the PBS group injected with PBS
the AS group injected with 250 ng purified angiostatin
and the AS group injected with 30 μg purified angiostatin. Reagents were injected intraperitoneally twice daily and tumor volume was calculated twice weekly for 21 d
then animals were sacrificed and each tumor specimen was divided into two parts after surgical resection. The first part was submitted to both immunocytochemistry for VEGF
VEGFR1
VEGFR2 and CD34
and TUNEL apoptosis assay. The second part was prepared for semi-quantitative RT-PCR analysis of VEGF
VEGFR1 and VEGFR2 mRNA abundance. Results There was an increase of apoptotic index (AI) (P0.05) in the AS (250 ng) group and in the AS (30 μg) group and there was a decrease of protein and mRNA expression levels of VEGF
VEGFR1 and VEGFR2
tumor volume and MVD (tumor angiogenesis was estimated by using CD34 antibody to determine microvessel density) (P0.05). These changes were more obvious in the the AS (30 μg) group than in the AS (250 ng) group(P0.05). Conclusion Angiostatin down-regulates vascular endothelial growth factor expression in human tongue squamous cell carcinoma cells in a dose-dependent manner.
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