Department of Morphology, Surgery and Experimental Medicine, Section of Anatomy and Histology, University of Ferrara, Ferrara, Italy.
Department of Biomedical and Specialty Surgical Sciences, University of Ferrara, Ferrara, Italy.
J Cell Mol Med. 2018 Jun;22(6):3149-3158. doi: 10.1111/jcmm.13594. Epub 2018 Mar 13.
It has been recently demonstrated that high pre-treatment levels of miR-29b positively correlated with the response of patients with acute myeloid leukaemia (AML) to hypomethylating agents. Upmodulation of miR-29b by restoring its transcriptional machinery appears indeed a tool to improve therapeutic response in AML. In cells from acute promyelocytic leukaemia (APL), miR-29b is regulated by PU.1, in turn upmodulated by agonists currently used to treat APL. We explored here the ability of PU.1 to also regulate miR-29b in non-APL cells, in order to identify agonists that, upmodulating PU.1 may be beneficial in hypomethylating agents-based therapies. We found that PU.1 may regulate miR-29b in the non-APL Kasumi-1 cells, showing the t(8;21) chromosomal rearrangement, which is prevalent in AML and correlated with a relatively low survival. We demonstrated that the PU.1-mediated contribution of the 2 miR-29b precursors is cell-related and almost completely dependent on adequate levels of Vav1. Nuclear PU.1/Vav1 association accompanies the transcription of miR-29b but, at variance with the APL-derived NB4 cells, in which the protein is required for the association of PU.1 with both miRNA promoters, Vav1 is part of molecular complexes to the PU.1 consensus site in Kasumi-1. Our results add new information on the transcriptional machinery that regulates miR-29b expression in AML-derived cells and may help in identifying drugs useful in upmodulation of this miRNA in pre-treatment of patients with non-APL leukaemia who can take advantage from hypomethylating agent-based therapies.
最近有研究表明,miR-29b 的高预处理水平与急性髓细胞白血病(AML)患者对低甲基化剂的反应呈正相关。通过恢复其转录机制上调 miR-29b 确实是提高 AML 治疗反应的一种手段。在急性早幼粒细胞白血病(APL)细胞中,miR-29b 受 PU.1 调控,而 PU.1 又被目前用于治疗 APL 的激动剂上调。我们在这里探讨了 PU.1 调节非 APL 细胞中 miR-29b 的能力,以确定激动剂上调 PU.1 可能对基于低甲基化剂的治疗有益。我们发现,PU.1 可能调节非 APL Kasumi-1 细胞中的 miR-29b,该细胞存在 t(8;21)染色体重排,该重排在 AML 中很常见,与相对较低的生存率相关。我们证明了 PU.1 介导的 2 个 miR-29b 前体的作用与细胞相关,几乎完全依赖于 Vav1 的适当水平。核 PU.1/Vav1 关联伴随着 miR-29b 的转录,但与源自 APL 的 NB4 细胞不同,在后者中,蛋白质是 PU.1 与两个 miRNA 启动子结合所必需的,而 Vav1 是与 PU.1 共识位点结合的分子复合物的一部分在 Kasumi-1 中。我们的研究结果为调节 AML 衍生细胞中 miR-29b 表达的转录机制提供了新的信息,并可能有助于确定在非 APL 白血病患者的预处理中上调这种 miRNA 的有用药物,这些患者可以从基于低甲基化剂的治疗中获益。