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聚合型精氨酸-甘氨酸-天冬氨酸(RGD)肽、聚(RGD)及其类似物的抗转移和抗侵袭作用

Anti-metastatic and anti-invasive effects of polymeric Arg-Gly-Asp (RGD) peptide, poly(RGD), and its analogues.

作者信息

Saiki I, Murata J, Matsuno K, Ogawa R, Nishi N, Tokura S, Azuma I

机构信息

Institute of Immunological Science, Hokkaido University, Sapporo.

出版信息

Jpn J Cancer Res. 1990 Jun-Jul;81(6-7):660-7. doi: 10.1111/j.1349-7006.1990.tb02624.x.

Abstract

We have investigated the anti-metastatic and anti-invasive activities of polypeptide analogues based on the Arg-Gly-Asp (RGD) adhesive signal in fibronectin, poly(RGD), poly(RGDS)[Arg-Gly-Asp-Ser] and poly(RGDT)[Arg-Gly-Asp-Thr]. These polypeptides containing repetitive RGD sequences were able to inhibit experimental and spontaneous lung metastases of B16-BL6 cells more effectively than the corresponding monomer peptides. In the spontaneous metastasis model, multiple i.v. administrations of these polymeric peptides before or after surgical excision of the primary tumor resulted in a significant reduction of lung tumor colonies. However, there was no significant difference in ability to inhibit spontaneous lung metastasis among poly(RGD), poly(RGDS) and poly(RGDT), although the carboxy-terminal amino acid residue (i.e., Xaa in -RGDXaa-) has been shown to play an important role in the expression of cell adhesive character. The treatment with poly(RGD) substantially prolonged the survival time for mice injected s.c. with B16-BL6 melanoma as compared with the untreated control. We also found that the polypeptides were potently able to inhibit the invasion and migration of tumor cells in vitro. Since these polypeptide analogues showed no antigenicity in the host and had no toxic effect on tumor cells in vitro, they may be potentially useful in the prevention of cancer metastasis.

摘要

我们研究了基于纤连蛋白中精氨酸 - 甘氨酸 - 天冬氨酸(RGD)黏附信号的多肽类似物——聚(RGD)、聚(RGDS)[精氨酸 - 甘氨酸 - 天冬氨酸 - 丝氨酸]和聚(RGDT)[精氨酸 - 甘氨酸 - 天冬氨酸 - 苏氨酸]的抗转移和抗侵袭活性。这些含有重复RGD序列的多肽比相应的单体肽更有效地抑制了B16 - BL6细胞的实验性和自发性肺转移。在自发性转移模型中,在原发性肿瘤手术切除之前或之后多次静脉注射这些聚合肽,导致肺肿瘤集落显著减少。然而,聚(RGD)、聚(RGDS)和聚(RGDT)在抑制自发性肺转移的能力上没有显著差异,尽管羧基末端氨基酸残基(即 -RGDXaa- 中的Xaa)已被证明在细胞黏附特性的表达中起重要作用。与未处理的对照组相比,用聚(RGD)处理显著延长了皮下注射B16 - BL6黑色素瘤小鼠的存活时间。我们还发现这些多肽能够有效抑制肿瘤细胞在体外的侵袭和迁移。由于这些多肽类似物在宿主中没有抗原性,并且在体外对肿瘤细胞没有毒性作用,它们可能在预防癌症转移方面具有潜在的用途。

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