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蕈样肉芽肿中Stat3缓慢迁移亚型的组成性激活:酪氨酸磷酸化抑制剂AG490抑制Stat3激活及蕈样肉芽肿肿瘤细胞系的生长

Constitutive activation of a slowly migrating isoform of Stat3 in mycosis fungoides: tyrphostin AG490 inhibits Stat3 activation and growth of mycosis fungoides tumor cell lines.

作者信息

Nielsen M, Kaltoft K, Nordahl M, Röpke C, Geisler C, Mustelin T, Dobson P, Svejgaard A, Odum N

机构信息

Institute of Medical Microbiology and Immunology, Section A, University of Copenhagen, 2200 N Copenhagen, Denmark.

出版信息

Proc Natl Acad Sci U S A. 1997 Jun 24;94(13):6764-9. doi: 10.1073/pnas.94.13.6764.

Abstract

Mycosis fungoides (MF) is a low-grade cutaneous T cell lymphoma of unknown etiology. In this report, the Jak/Stat (Janus kinase/signal transducer and activator of transcription) signaling pathway was investigated in tumor cell lines established from skin biopsy specimens from a patient with MF. Jaks link cytokine receptors to Stats, and abnormal Jak/Stat signaling has been observed in some hemopoietic cancers. In MF tumor cells, a slowly migrating isoform of Stat3, Stat3(sm), was found to be constitutively activated, i.e., (i) Stat3(sm) was constitutively phosphorylated on tyrosine residues, and tyrosine phosphorylation was not enhanced by growth factor stimulation; (ii) band shift assays and immunoprecipitations of DNA/Stat complexes showed constitutive DNA-binding properties of Stat3(sm); and (iii) Stat3(sm) was constitutively associated with Jak3. The abnormal activation of Stat3(sm) was highly specific. Thus, neither the fast migrating isoform of Stat3 (Stat3(fm)) nor other Stats (Stat1, Stat2, and Stat4 through Stat6) were constitutively activated. The Jak kinase inhibitor, tyrphostin AG490, blocked the constitutive activation of Stat3(sm) and inhibited spontaneous as well as interleukin 2-induced growth of MF tumor cells. In conclusion, we have provided evidence for an abnormal Jak/Stat signaling and growth regulation in tumor cells obtained from affected skin of an MF patient.

摘要

蕈样肉芽肿(MF)是一种病因不明的低度皮肤T细胞淋巴瘤。在本报告中,对从一名MF患者皮肤活检标本建立的肿瘤细胞系中的Jak/Stat(Janus激酶/信号转导和转录激活因子)信号通路进行了研究。Jaks将细胞因子受体与Stats连接起来,并且在一些血液系统癌症中观察到了异常的Jak/Stat信号传导。在MF肿瘤细胞中,发现Stat3的一种慢迁移异构体Stat3(sm)被组成性激活,即:(i)Stat3(sm)在酪氨酸残基上被组成性磷酸化,并且生长因子刺激不会增强酪氨酸磷酸化;(ii)DNA/Stat复合物的凝胶迁移分析和免疫沉淀显示Stat3(sm)具有组成性DNA结合特性;以及(iii)Stat3(sm)与Jak3组成性相关。Stat3(sm)的异常激活具有高度特异性。因此,Stat3的快迁移异构体(Stat3(fm))以及其他Stats(Stat1、Stat2以及Stat4至Stat6)均未被组成性激活。Jak激酶抑制剂 tyrphostin AG490阻断了Stat3(sm)的组成性激活,并抑制了MF肿瘤细胞的自发生长以及白细胞介素2诱导的生长。总之,我们为从MF患者受累皮肤获得的肿瘤细胞中存在异常的Jak/Stat信号传导和生长调节提供了证据。

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