Inhibition of angiogenesis in vitro and in vivo: Comparison of the relative activities of triflavin, an Arg-Gly-Asp-containing peptide and anti-α(v)β3 integrin monoclonal antibody

Joen Rong Sheu, Mao Hsiung Yen, Ya Chen Kan, Wei Chun Hung, Pei Te Chang, Hsiang Ning Luk

研究成果: 雜誌貢獻文章同行評審

87 引文 斯高帕斯(Scopus)


Disintegrin which contains the amino acid sequence Arg-Gly-Asp (RGD), has been implicated as a recognition site in interactions between extracellular matrix (ECM) and cell membrane receptors. Triflavin, a 7.5 kDa cysteine-rich polypeptide purified from Trimeresurus flavoviridis snake venom, belongs to a family of disintegrins. Integrin α(v)β3 has recently been identified as a marker of angiogenic blood vessels and therefore anti-α(v)β3 mAb may significantly inhibit angiogenesis. Therefore, this study was designed to compare the relative activity of triflavin and anti-α(v)β3 mAb in human umbilical vein endothelial cell (HUVEC) adhesion and migration in vitro, and on angiogenesis induced by TNF(α) in chicken chorioallantoic membrane (CAM). In this study, it was shown that triflavin (0.1 to 0.4 μM) dose-dependently inhibited the adhesion of HUVECs to ECMs (i.e., vitronectin, fibronectin, laminin and collagen type IV). At a concentration of 10 μM, anti-α(v)β3 mAb almost completely inhibited the adhesion of cells to vitronectin, had a moderate inhibitory effect on fibronectin and laminin, but only a slight inhibitory effect on collagen type IV. On the other hand, vitronectin and fibronectin promote a significantly greater extent of cell adhesion and migration than laminin or collagen type IV over a wide range of concentrations (5 to 15 μg/ml). In cell migration studies, triflavin (0.4 μM) inhibited more markedly vitronectin- and fibronectin-mediated migration than that mediated by laminin- and collagen type IV. Comparison of the relative effectiveness of triflavin with anti-α(v)β3 mAb, showed that triflavin was at least twenty to thirty times more potent than anti-α(v)β3 mAb at inhibiting cell adhesion and migration. Furthermore, we used TNF(α) as an inducer of angiogenesis in the CAM assay. Close examination of the effects of triflavin and anti-α(v)β3 mAb on TNF(α)-induced angiogenesis revealed the presence of discontinuous and disrupted blood vessels. However, anti-α(v)β3 mAb showed a significant effect only at a higher concentration (10 μM). These results suggest that the inhibition of angiogenesis may have been due to interference with the adhesion and migration of endothelial cells to ECMs. The results also indicate that triflavin has a more powerful inhibitory effect than anti-α(v)β3 mAb on angiogenesis, suggesting that triflavin could theoretically be used as a reasonable therapeutic adjuvant for therapy or prevention of angiogenesis-induced diseases.

頁(從 - 到)445-454
期刊Biochimica et Biophysica Acta - General Subjects
出版狀態已發佈 - 十月 20 1997

ASJC Scopus subject areas

  • 生物物理學
  • 生物化學
  • 分子生物學


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