HUMAN-MELANOMA CELLS EXPRESS FUNCTIONAL ENDOTHELIN-1 RECEPTORS

被引:54
|
作者
YOHN, JJ
SMITH, C
STEVENS, T
HOFFMAN, TA
MORELLI, JG
HURT, DL
YANAGISAWA, M
KANE, MA
ZAMORA, MR
机构
[1] UNIV COLORADO,SCH MED,DEPT MED,BOULDER,CO 80309
[2] VET AFFAIRS MED CTR,DENVER,CO
[3] UNIV COLORADO,CTR CANC,DENVER,CO 80262
[4] UNIV TEXAS,SW MED CTR,HOWARD HUGHES MED INST,DALLAS,TX 75235
关键词
D O I
10.1006/bbrc.1994.1722
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Current evidence suggests that endothelium-derived factors enhance human melanoma vascular invasion. Therefore, we studied human melanoma cell expression of receptors to the endothelium-derived peptide, endothelin-1 (ET-1), and determined if they respond to ET-1 with proliferation and chemokinesis. Human metastatic melanoma cell lines were found to have specific, saturable, high affinity ET-1 binding. Northern analysis and competitive inhibition studies confirmed that melanoma cells express the ET(B) receptor isoform. Ten nanomolar ET-1 caused an 8.2 to 25.5-fold increase in intracellular free calcium. ET-1 was found to be a weak mitogen for melanoma cells, however, melanoma cell chemokinesis was significantly increased by ET-1. These data suggest that ET-1 may be involved in providing a chemokinetic and growth factor environment that enhances perivascular proliferation and invasiveness of melanoma cells. (C) 1994 Academic Press, Inc.
引用
收藏
页码:449 / 457
页数:9
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