来自天然蛋白质的崩解素样肽:一种建议的辅助治疗癌症:评论

Mizejewski Gj
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引用次数: 2

摘要

崩解素由一组小蛋白质或肽(45-85个氨基酸)组成,作为整合素受体依赖性细胞活性的天然拮抗剂。整合素本身包含一个异二聚体(α链和β链)跨膜细胞表面受体超家族,其功能包括细胞粘附、生长、迁移和血管生成。相反,分解素由两种类型的分子组成,即a)含有昆虫和动物毒液的短蛋白或肽;b)存在于大型哺乳动物金属蛋白酶上的内在亚结构域序列片段或短基序。某些崩解素特异性结合位于杂合体受体的整合素β -1和β -3链上的三氨基酸序列(RGD, LGD等)。这些位点的结合可以抑制或阻断细胞迁移、血管生成、转移和血小板聚集。最近,来自天然蛋白质的小的崩解素样肽同样被报道抑制与整合素依赖性细胞活性相关的生长和粘附功能。本报告描述了这种崩解素样肽的例子,并为其在辅助癌症治疗中的应用提供了支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Disintegrin-Like Peptides Derived from Naturally-Occurring Proteins: A Proposed Adjunct Treatment for Cancer Therapy: A Commentary
Disintegrins constitute a group of small proteins or peptides (45-85 amino acids) that function as natural antagonists of integrin receptor-dependent cell activities. The integrins themselves comprise a superfamily of hetero-dimeric (alpha and beta chains) transmembrane cell surface receptors whose functions include cell adhesion, growth, migration, and angiogenesis. In contrast, the disintegrins comprise groups of two types of molecules, namely, a) short proteins or peptides comprising insect and animal venoms; and b) intrinsic sub domain sequence fragments or short motifs present on large mammalian metalloprotease enzymes. Certain disintegrins bind specifically to tri-amino acid sequences (RGD, LGD etc) located on integrins beta-1 and beta-3 chains of the hetero complex receptors. Binding at such sites can inhibit or block cell migration, angiogenesis, metastasis, and platelet aggregation. Recently, small disintegrin-like peptides from naturally-occurring proteins have likewise been reported to inhibit growth and adhesion functions associated with integrin-dependent cell activities. The present report describes examples of such disintegrin-like peptides and provides support for their proposed use in adjunct cancer therapy.
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