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Assessing IRAK4 Functions in ABC DLBCL by IRAK4 Kinase Inhibition and Protein Degradation

机译:通过Irak4激酶抑制和蛋白质降解评估ABC DLBCL中的Irak4功能

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The interleukin-1 receptor-activated kinase 4 (IRAK4) belongs to the IRAK family of serine/threonine kinases and plays a central role in the innate immune response. However, the function of IRAK4 in tumor growth and progression remains elusive. Here we sought to determine the enzymatic and scaffolding functions of IRAK4 in activated B-cell-like diffuse large B cell lymphoma (ABC DLBCL). We chose a highly selective IRAK4 kinase inhibitor to probe the biological effects of kinase inhibition and developed a series of IRAK4 degraders to evaluate the effects of protein degradation in ABC DLBCL cells. Interestingly, the results demonstrated that neither IRAK4 kinase inhibition nor protein degradation led to cell death or growth inhibition, suggesting a redundant role for IRAK4 in ABC DLBCL cell survival. IRAK4 degraders characterized in this study provide useful tools for understanding IRAK4 protein scaffolding function, which was previously unachievable using pharmacological perturbation.
机译:白细胞介素-1受体激活激酶4(IRAK4)属于丝氨酸/苏氨酸激酶的IRAK家族,在先天性免疫反应中起着核心作用。然而,IRAK4在肿瘤生长和进展中的作用仍不清楚。在这里,我们试图确定IRAK4在活化的B细胞样弥漫性大B细胞淋巴瘤(ABC-DLBCL)中的酶和支架功能。我们选择了一种高选择性的IRAK4激酶抑制剂来探索激酶抑制的生物学效应,并开发了一系列IRAK4降解剂来评估蛋白质降解对ABC-DLBCL细胞的影响。有趣的是,结果表明,无论是IRAK4激酶抑制还是蛋白质降解都不会导致细胞死亡或生长抑制,这表明IRAK4在ABC-DLBCL细胞存活中起着冗余作用。本研究中描述的IRAK4降解物为理解IRAK4蛋白支架功能提供了有用的工具,而这一功能以前无法通过药理学扰动实现。

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