首页> 美国卫生研究院文献>The Journal of Biological Chemistry >CUEDC2 (CUE Domain-containing 2) and SOCS3 (Suppressors of Cytokine Signaling 3) Cooperate to Negatively Regulate Janus Kinase 1/Signal Transducers and Activators of Transcription 3 Signaling
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CUEDC2 (CUE Domain-containing 2) and SOCS3 (Suppressors of Cytokine Signaling 3) Cooperate to Negatively Regulate Janus Kinase 1/Signal Transducers and Activators of Transcription 3 Signaling

机译:CUEDC2(含CUE域2)和SOCS3(细胞因子信号转导3的抑制剂)协同负调节Janus激酶1 /信号转导子和转录3信号转导激活剂。

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摘要

Janus kinase 1/signal transducers and activators of transcription 3 (JAK1/STAT3) pathway is one of the recognized oncogenic signaling pathways that frequently overactivated in a variety of human tumors. Despite rapid progress in elucidating the molecular mechanisms of activation of JAK/STAT pathway, the processes that regulate JAK/STAT deactivation need to be further clarified. Here we demonstrate that CUE domain-containing 2 (CUEDC2) inhibits cytokine-induced phosphorylation of JAK1 and STAT3 and the subsequent STAT3 transcriptional activity. Further analysis by a yeast two-hybrid assay showed that CUEDC2 could engage in a specific interaction with a key JAK/STAT inhibitor, SOCS3 (suppressors of cytokine signaling 3). The interaction between CUEDC2 and SOCS3 is required for the inhibitory effect of CUEDC2 on JAK1 and STAT3 activity. Additionally, we found CUEDC2 functions collaboratively with SOCS3 to inhibit JAK1/STAT3 signaling by increasing SOCS3 stability via enhancing its association with Elongin C. Therefore, our findings revealed a new biological activity for CUEDC2 as the regulator of JAK1/STAT3 signaling and paved the way to a better understanding of the mechanisms by which SOCS3 has been linked to suppression of the JAK/STAT pathway.
机译:Janus激酶1 /信号转导子和转录激活因子3(JAK1 / STAT3)途径是公认的致癌信号传导途径之一,在多种人类肿瘤中经常被过度活化。尽管阐明JAK / STAT途径激活的分子机制方面取得了迅速的进展,但调节JAK / STAT失活的过程仍需要进一步阐明。在这里,我们证明含CUE域2(CUEDC2)抑制细胞因子诱导的JAK1和STAT3的磷酸化以及随后的STAT3转录活性。通过酵母双杂交测定法的进一步分析表明,CUEDC2可以与关键的JAK / STAT抑制剂SOCS3(细胞因子信号传导抑制剂3)发生特异性相互作用。 CUEDC2与SOCS3之间的相互作用是CUEDC2对JAK1和STAT3活性的抑制作用所必需的。此外,我们发现CUEDC2与SOCS3协同发挥作用,通过增强SOCS3与Elongin C的结合来增加SOCS3的稳定性,从而抑制JAK1 / STAT3信号传导。以便更好地了解SOCS3与抑制JAK / STAT途径相关的机制。

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