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The involvement of JAK-STAT3 in cell motility, invasion, and metastasis

机译:JAK-STAT3参与细胞活性,入侵和转移

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摘要

JAK-STAT3 signaling, while regulating many aspects of cancer development and progression, promotes invasion and metastasis through activation of key metastasis promoting genes such as WASF3. STAT3 promotes WASF3 expression and JAK2 independently activates it, which is required for invasion. JAK-STAT3 signaling is dependent on WASF3 function, since its inactivation in cells expressing JAK-STAT3 suppresses invasion. WASF3 overexpression leads to activation of NFκB and ZEB1 which also promote invasionthrough regulation of target genes involved in metastasis. NFκB frequently cooperates with STAT3 to upregulate metastasis promoting genes such as matrix metalloproteinases and cytokines, as well as to suppress microRNAs which can suppresses invasion. This better understanding of the complex role played by JAK-STAT3 in the regulation of cell movement, invasion, and metastasis provides opportunities to suppress this lethal aspect of cancer progression by not only targeting the JAK and STAT3 proteins directly, but also some of the downstream effectors of JAK-STAT3 signaling.
机译:JAK-STAT3信号,调节许多方面癌症的发展和发展,促进通过激活入侵和转移的关键如WASF3转移促进基因。促进WASF3表达式和JAK2独立需要激活,这是入侵。JAK-STAT3信号依赖于WASF3功能,因为其在细胞失活表达JAK-STAT3抑制入侵。过度导致NFκB和激活ZEB1也促进invasionthrough调节目标基因转移。移植转移促进基因等基质金属蛋白酶和细胞因子抑制小分子核糖核酸可以抑制入侵。复杂JAK-STAT3所扮演的角色调节细胞运动、入侵和抑制转移提供了机会这致命的癌症恶化只针对木菠萝和STAT3蛋白直接,而且一些下游效应器JAK-STAT3信号。

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