In vivo binding of the radioiodinated peptide YIGSR on B16 melanoma cells.

Invasion & metastasis Pub Date : 1996-01-01
K Kouzi-Koliakos, G Koliakos, C Trontzos, A Papageorgiou, S Iliadis, A Triantos, A Dimitriadou, M Kanellaki
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Abstract

It has been reported that metastatic melanoma cell lines selectively bind in vitro with the synthetic laminin pentapeptide tyrosyl-isoleucyl-glycyl-seryl-arginine (YIGSR). The aim of this study was to investigate whether the same peptide can bind on melanoma cells in vivo as well. Iodine-125-labeled YIGSR was administered to B16 melanoma-bearing animals. Microscopic autoradiography of tumor and organ sections taken 24 h after peptide administration showed that the peptide did accumulate on the surface of certain tumor cells. The peptide binding cells were frequent in metastatic sites and tumors grown for 24 days and rare in tumors grown for 10 days. A similarly radiolabeled control pentapeptide (peptide DRLKY) did not bind to any tumor cell. It is suggested that the YIGSR binding tumor cells may represent a distinct melanoma cell population with a high metastatic potential.

放射性碘化肽YIGSR在B16黑色素瘤细胞上的体内结合。
据报道,转移性黑色素瘤细胞系在体外选择性结合合成的层粘连蛋白五肽酪氨酸异亮氨酸甘酰基丝氨酸精氨酸(YIGSR)。本研究的目的是研究相同的肽是否也能在体内结合黑色素瘤细胞。将碘125标记的YIGSR用于B16黑色素瘤动物。给药24小时后肿瘤和器官切片的显微放射自显像显示肽确实在某些肿瘤细胞表面积聚。肽结合细胞在转移部位和生长24天的肿瘤中很常见,在生长10天的肿瘤中很少见。一个类似的放射标记的对照五肽(肽DRLKY)不与任何肿瘤细胞结合。这表明,结合YIGSR的肿瘤细胞可能代表了一种具有高转移潜力的独特黑色素瘤细胞群。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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