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一种来自纤连蛋白的合成肽可抑制小鼠黑色素瘤细胞的实验性转移。

A synthetic peptide from fibronectin inhibits experimental metastasis of murine melanoma cells.

作者信息

Humphries M J, Olden K, Yamada K M

出版信息

Science. 1986 Jul 25;233(4762):467-70. doi: 10.1126/science.3726541.

Abstract

Adhesive interactions between cells and the extracellular matrix occur at several stages of metastasis. Such interactions might be inhibited by synthetic peptide probes derived from the cell-binding regions of matrix molecules. Gly-Arg-Gly-Asp-Ser (GRGDS) is a pentapeptide sequence that appears to be critical for cell interaction with fibronectin. Coinjection of GRGDS with B16-F10 murine melanoma cells dramatically inhibited the formation of lung colonies in C57BL/6 mice. Two closely related control peptides, in which specific amino acids within the GRGDS sequence were transposed or substituted, displayed little or no activity. Inhibition by GRGDS was dose-dependent, noncytotoxic, and did not result from an impairment of cellular tumorigenicity. GRGDS may function by inhibiting tumor cell retention in the lung since radiolabeled B16-F10 tumor cells injected with the peptide were lost at a substantially greater rate than control cells.

摘要

细胞与细胞外基质之间的黏附相互作用发生在转移的多个阶段。此类相互作用可能会被源自基质分子细胞结合区域的合成肽探针所抑制。甘氨酸 - 精氨酸 - 甘氨酸 - 天冬氨酸 - 丝氨酸(GRGDS)是一个五肽序列,它似乎对细胞与纤连蛋白的相互作用至关重要。将GRGDS与B16 - F10小鼠黑色素瘤细胞共同注射,可显著抑制C57BL / 6小鼠肺部菌落的形成。两个密切相关的对照肽,其中GRGDS序列内的特定氨基酸被置换或取代,几乎没有活性。GRGDS的抑制作用是剂量依赖性的,无细胞毒性,且不是由细胞致瘤性受损所致。GRGDS可能通过抑制肿瘤细胞在肺部的滞留起作用,因为注射了该肽的放射性标记B16 - F10肿瘤细胞的丢失速度比对照细胞快得多。

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