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Raf和Ras癌基因快速诱导肝素结合表皮生长因子/白喉毒素受体表达。

Rapid induction of heparin-binding epidermal growth factor/diphtheria toxin receptor expression by Raf and Ras oncogenes.

作者信息

McCarthy S A, Samuels M L, Pritchard C A, Abraham J A, McMahon M

机构信息

DNAX Research Institute, Palo Alto, California 94304, USA.

出版信息

Genes Dev. 1995 Aug 15;9(16):1953-64. doi: 10.1101/gad.9.16.1953.

Abstract

We have used differential display PCR to search for mRNAs induced by delta Raf-1:ER, an estradiol-dependent form of Raf-1 kinase. Through this approach the gene encoding heparin-binding epidermal growth factor (HB-EGF) was identified as an immediate-early transcriptional target of oncogenic Raf kinases. Activation of delta Raf-1:ER and a conditional oncogenic form of B-Raf, delta B-RAF:ER, resulted in rapid and sustained induction of HB-EGF mRNA expression and secretion of mature HB-EGF from cells. Neutralizing anti-HB-EGF antisera prevented the delayed activation of the c-Jun amino-terminal kinases that is observed in cells transformed by delta Raf-1:ER. These results demonstrate that distinct signaling pathways can cross talk via the secretion of polypeptide growth factors. Furthermore, cells transformed by oncogenic Ras, which also induced HB-EGF expression, demonstrated a marked increase in sensitivity to the cytotoxic action of diphtheria toxin, for which the membrane anchored HB-EGF precursor acts as a cell-surface receptor.

摘要

我们利用差异显示PCR技术来寻找由δRaf-1:ER(一种雌激素依赖性的Raf-1激酶形式)诱导的mRNA。通过这种方法,编码肝素结合表皮生长因子(HB-EGF)的基因被鉴定为致癌性Raf激酶的一个即时早期转录靶点。δRaf-1:ER和B-Raf的一种条件致癌形式δB-RAF:ER的激活,导致HB-EGF mRNA表达的快速持续诱导以及细胞中成熟HB-EGF的分泌。中和抗HB-EGF抗血清可阻止在由δRaf-1:ER转化的细胞中观察到的c-Jun氨基末端激酶的延迟激活。这些结果表明,不同的信号通路可以通过多肽生长因子的分泌相互作用。此外,由致癌性Ras转化的细胞也诱导了HB-EGF的表达,对白喉毒素的细胞毒性作用表现出显著的敏感性增加,而膜锚定的HB-EGF前体作为细胞表面受体介导了这种作用。

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