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学会・研究発表

血管新生阻害活性を有するサメ抽出脂質のメカニズムと臨床への応用

2006年3月9日、GTCbioによってアメリカ・サンディエゴで開催されたAngiogenesis research & Theraputicsのポスターセッションで、強い血管新生阻害活性を有するサメ抽出脂質のメカニズムと臨床への応用についての発表がありました。

Angiogenesis research & Theraputics 2006

An ethanolic extract from a marine fish having potent anti-angiogenic activity: its anti-angiogenic mechanism and clinical application.

In-Sook Ahn1, Steven Grekin2, Stephen Verral2 and John Croft3

  1. Dpt. of Food Science and Nutrition Pusan National University
  2. Grekin Skin Institute Oakwood Southshore Medical Center Wyandotte Michigan
  3. Immuno research Ltd. Auckland, New Zealand
Abstract

An ethanol extract from shark muscle has been shown to have potent angiogenic activity when mixed together with olive oil in a ratio of 1part extract to 9 parts olive oil. This mixture has been given the trade name SuperMaco (SMO).

The anti-angiogenic activity was evident in both in vitro and in vivo studies in rats. When combined with the known angiogenic stimulatory growth factors Vascular Endothelial Growth Factor (VEGF), Platelet Derived Growth Factor (PDGF), Transforming Growth Factor-Beta ( TGF-β) and Fibroblast Growth Factor -2 (FGF-2), SMO completely eliminated the stimulation induced by these growth factors. Possible mechanisms for this activity are that SMO is competing for receptor sites on the endothelial cell surface by preferential binding to those sites or by binding to the growth factors themselves.

Studies were conducted using soluble forms of VEGF-R1 and VEGF-R2 and it was found that SMO inhibited complex formation of the VEGF with both receptors. This inhibitory effect by SMO was enhanced when SMO was pre-incubated with VEGF receptors.

In another study, the effect of SMO on VEGF receptor phosphorylation using human umbilical vein endothelial cells (HUVEC) and a human breast carcinoma cell line (MDA-MB-231) was investigated. The in vitro cell proliferation assay indicated that SMO reversed the increase in VEGF promoted cell proliferation in both HUVEC and MDA-MB-231 cells. Using Western Blot analysis it was observed that SMO significantly inhibited VEGF promoted VEGF receptor-1 , VEGF receptor-2 and tyrosine phosphorylation in HUVEC and MDA-MB-231 cells in a dose related manner. These results suggest that SMO appears to block the binding of VEGF with the receptors and inhibit the signal transduction pathways.