Increased expression of insulin receptor substrate-1 in human pancreatic cancer

被引:72
作者
Bergmann, U
Funatomi, H
Kornmann, M
Beger, HG
Korc, M
机构
[1] UNIV CALIF IRVINE,DIV ENDOCRINOL DIABET & METAB,IRVINE,CA 92717
[2] UNIV ULM,DEPT GEN SURG,D-89075 ULM,GERMANY
关键词
D O I
10.1006/bbrc.1996.0500
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
Insulin receptor substrate-1 (IRS-1) is a multisite docking protein implicated in mitogenic signaling following activation of the insulin and insulin-like growth factor I receptors. In the present study we characterized IRS-1 expression in human pancreatic cancer. Northern blot analysis revealed high levels of IRS-1 mRNA transcripts in ASPC-1 and MIA PaCa-2 human pancreatic cancer cell lines, and lower levels in COLO-357. PANC-1, and T3M4 cells. Immunoblotting with anti-IRS-1 antibodies indicated that IRS-1 protein levels paralleled IRS-1 mRNA levels. Analysis of RNA isolated from normal and cancerous human pancreatic tissues indicated that 7 of 16 pancreatic cancer samples overexpressed IRS-1 mRNA transcripts by comparison with the normal pancreas and that insulin mRNA levels were abundant in many tumors. These data suggest that IRS-1 contributes to the signaling pathways that lead to excessive growth stimulation in human pancreatic cancer. (C) 1996 Academic Press, Inc.
引用
收藏
页码:886 / 890
页数:5
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