CTBP脱氢酶抑制剂MTOB和4-Cl-HIPP的特异性。

microPublication biology Pub Date : 2025-02-03 eCollection Date: 2025-01-01 DOI:10.17912/micropub.biology.001415
Benjamin A Stickland, Franziska Greulich, Nina Henriette Uhlenhaut
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引用次数: 0

摘要

c端结合蛋白(ctbp)是在癌症和炎症中重要的保守转录抑制因子。在转录共调节因子中,ctbp具有一个功能性脱氢酶结构域。由于多种恶性肿瘤显示CTBP水平升高,针对该脱氢酶结构域的CTBP抑制剂已被开发出来。虽然CTBP脱氢酶功能在转录调控中的重要性尚不清楚,但一些研究依赖于CTBP抑制剂。体外实验证实了这些化合物与CTBP活性部位的结合,但缺乏特异性的证据。为了解决这个问题,我们用MTOB或4-Cl-HIPP处理野生型和Ctbp1, 2双敲除J774.1细胞,并进行rna测序。我们观察到,这两种抑制剂引起不同的转录变化,表明非重叠的作用模式。此外,两种抑制剂诱导的大部分变化都发生在Ctbp1/2双敲除细胞中,提示脱靶效应。我们假设这些CTBP脱氢酶抑制剂对CTBP缺乏特异性,并强调仔细重新评估使用这些抑制剂的研究结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The specificity of CTBP dehydrogenase inhibitors MTOB and 4-Cl-HIPP.

C-terminal binding proteins (CTBPs) are conserved transcriptional repressors important in cancer and inflammation. Uniquely amongst transcriptional co-regulators, CTBPs possess a functional dehydrogenase domain. Since multiple malignancies display elevated CTBP levels, CTBP inhibitors targeting this dehydrogenase domain have been developed. While the importance of CTBPs dehydrogenase function for transcriptional regulation remains unclear, several studies have relied on CTBP inhibitors. In vitro experiments have confirmed binding of these compounds to CTBP's active site, however evidence for specificity is lacking. To address this, we treated wildtype and Ctbp1 , 2 double knockout J774.1 cells with MTOB or 4-Cl-HIPP and performed RNA-seq. We observed that both inhibitors elicit distinct transcriptional changes indicating non-overlapping modes of action. Moreover, the majority of changes induced by either inhibitor are observed in Ctbp1/2 double knockout cells suggesting off-target effects. We hypothesize that those CTBP dehydrogenase inhibitors lack specificity to CTBPs and emphasise careful revaluation of findings inferred from studies using those inhibitors.

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