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Src 家族蛋白激酶抑制剂以依赖 p300 的方式抑制 MYB 活性。

Src-Family Protein Kinase Inhibitors Suppress MYB Activity in a p300-Dependent Manner.

机构信息

Institute for Biochemistry, Westfälische-Wilhelms-Universität, D-48149 Münster, Germany.

出版信息

Cells. 2022 Mar 30;11(7):1162. doi: 10.3390/cells11071162.

Abstract

Recent studies have disclosed transcription factor MYB as a potential drug target for malignancies that are dependent on deregulated MYB function, including acute myeloid leukemia (AML) and adenoid cystic carcinoma (ACC). Although transcription factors are often regarded as undruggable, successful targeting of MYB by low-molecular-weight compounds has recently been demonstrated. In an attempt to repurpose known drugs as novel MYB-inhibitory agents, we have screened libraries of approved drugs and drug-like compounds for molecules with MYB-inhibitory potential. Here, we present initial evidence for the MYB-inhibitory activity of the protein kinase inhibitors bosutinib, PD180970 and PD161570, that we identified in a recent screen. We show that these compounds interfere with the activity of the MYB transactivation domain, apparently by disturbing the ability of MYB to cooperate with the coactivator p300. We show that treatment of the AML cell line HL60 with these compounds triggers the up-regulation of the myeloid differentiation marker CD11b and induces cell death. Importantly, we show that these effects are significantly dampened by forced expression of an activated version of MYB, confirming that the ability to suppress MYB function is a relevant activity of these compounds. Overall, our work identifies several protein kinase inhibitors as novel MYB-inhibitory agents and suggests that the inhibition of MYB function may play a role in their pharmacological impact on leukemic cells.

摘要

最近的研究揭示了转录因子 MYB 作为依赖于失调的 MYB 功能的恶性肿瘤的潜在药物靶点,包括急性髓系白血病 (AML) 和腺样囊性癌 (ACC)。尽管转录因子通常被认为是不可成药的,但最近已经证明了低分子量化合物对 MYB 的成功靶向。为了将已知药物重新用作新型 MYB 抑制性药物,我们筛选了已批准药物和类药物化合物的文库,以寻找具有 MYB 抑制潜力的分子。在这里,我们提出了我们在最近的筛选中发现的蛋白激酶抑制剂博舒替尼、PD180970 和 PD161570 具有 MYB 抑制活性的初步证据。我们表明,这些化合物干扰 MYB 转录激活结构域的活性,显然是通过干扰 MYB 与共激活因子 p300 合作的能力。我们表明,这些化合物处理 AML 细胞系 HL60 会触发髓样分化标志物 CD11b 的上调,并诱导细胞死亡。重要的是,我们表明通过强制表达激活形式的 MYB 可以显著抑制这些作用,证实抑制 MYB 功能的能力是这些化合物的相关活性。总的来说,我们的工作确定了几种蛋白激酶抑制剂作为新型 MYB 抑制性药物,并表明抑制 MYB 功能可能在它们对白血病细胞的药理作用中发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10d0/8997952/d534c2309c2f/cells-11-01162-g001.jpg

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