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组成性激活的Stat3的抑制与蕈样肉芽肿肿瘤细胞中Bcl-2/Bax表达的改变及细胞凋亡的诱导相关。

Inhibition of constitutively activated Stat3 correlates with altered Bcl-2/Bax expression and induction of apoptosis in mycosis fungoides tumor cells.

作者信息

Nielsen M, Kaestel C G, Eriksen K W, Woetmann A, Stokkedal T, Kaltoft K, Geisler C, Röpke C, Odum N

机构信息

Institute of Medical Microbiology and Immunology, University of Copenhagen, Denmark.

出版信息

Leukemia. 1999 May;13(5):735-8. doi: 10.1038/sj.leu.2401415.

Abstract

The Jak/Stat signaling pathway transmits signals from many cytokine and growth factor receptors to target genes in the nucleus. Constitutive activation of Stat3 has recently been observed in many tumor cells and dysregulation of the Stat signaling pathway has been proposed to be implicated in malignant transformation. In a previous study, we found constitutively tyrosine phosphorylated Stat3 in mycosis fungoides tumor cells. Here, we show that the Jak kinase inhibitor, Ag490, inhibits the constitutive binding of Stat3 to an oligonucleotide representing the Stat-binding sequence from the ICAM promotor. The decreased ability of Stat3 to bind DNA precedes dynamic alterations in the expression of anti-apoptotic Bcl-2 and pro-apoptotic Bax proteins (decreased Bcl-2 expression and increased Bax expression) and induction of apoptosis. Thus, our data suggest that the involvement of Stat3 in oncogenic transformation could be mediated through regulation of survival signals.

摘要

Jak/Stat信号通路将来自许多细胞因子和生长因子受体的信号传递至细胞核中的靶基因。最近在许多肿瘤细胞中观察到Stat3的组成性激活,并且有人提出Stat信号通路的失调与恶性转化有关。在先前的研究中,我们在蕈样肉芽肿肿瘤细胞中发现了组成性酪氨酸磷酸化的Stat3。在此,我们表明Jak激酶抑制剂Ag490可抑制Stat3与代表ICAM启动子中Stat结合序列的寡核苷酸的组成性结合。Stat3与DNA结合能力的下降先于抗凋亡Bcl-2和促凋亡Bax蛋白表达的动态变化(Bcl-2表达降低和Bax表达增加)以及细胞凋亡的诱导。因此,我们的数据表明Stat3参与致癌转化可能是通过调节生存信号来介导的。

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