Department of Life Science and Biotechnology, Shanghai Jiao Tong University School, 800 Dongchuan Road, Shanghai, 200240, China; Department of Biology, College of Life Sciences, Shanghai Normal University, Shanghai, 200234, China; Department of Biochemistry and Molecular Cell Biology, Key Laboratory of Cell Differentiation and Apoptosis of Chinese Ministry of Education, Shanghai Key Laboratory for Tumor Microenvironment and Inflammation, Shanghai Jiao Tong University School of Medicine, 280 S. Chongqing Road, Shanghai, 200025, China.
Department of Biology, College of Life Sciences, Shanghai Normal University, Shanghai, 200234, China.
Biochem Biophys Res Commun. 2022 Mar 12;596:36-42. doi: 10.1016/j.bbrc.2022.01.081. Epub 2022 Jan 25.
Both MLL-AF9 and MLL-ENL leukemia fusion proteins drive oncogenic transformation of hematopoietic cells through their N-terminal DNA/histone binding mixed-lineage leukemia 1 domain and C-terminal fragment of AF9 or ENL containing an unstructured linker region and the ANC1 homology domain, which recruits transcription factors. Despite of their structural similarity, acute myeloid leukemia (AML) patients bearing MLL-ENL show more adverse outcomes compared to those with MLL-AF9. We recapitulated the clinical patterns of these two MLL-fusions driven AMLs using murine models and found that MLL-ENL AML cells showed slower cell cycle progression and more resistance to standard chemotherapy than MLL-AF9 cells. These phenotypes were primarily controlled by the linker regions of ENL and a highly conserved lysine residue K469 within. Substitution of K469 with an acetylated mimic glutamine abolished the ability of MLL-ENL to suppress proliferation and promote chemo-resistance. We showed that deacetylase Sirt2 might act as an upstream regulator of MLL-ENL. Deletion of Sirt2 promoted proliferation of AML cells with either MLL fusions. Importantly, loss of Sirt2 greatly enhanced the sensitivity of the MLL-ENL AML cells to chemo-treatment. Taken together, our study uncovered a unique regulatory role of Sirt2 in leukemogenesis and suggested targeting SIRT2 as a new way to sensitize MLL-ENL AML patience for chemotherapy.
MLL-AF9 和 MLL-ENL 白血病融合蛋白通过其 N 端 DNA/组蛋白结合混合谱系白血病 1 结构域和 C 端 AF9 或 ENL 的片段驱动造血细胞的致癌转化,该片段包含无规卷曲结构域和 ANC1 同源结构域,募集转录因子。尽管它们具有结构相似性,但携带 MLL-ENL 的急性髓系白血病 (AML) 患者的预后比携带 MLL-AF9 的患者更差。我们使用小鼠模型重现了这两种由 MLL 融合驱动的 AML 的临床模式,发现 MLL-ENL AML 细胞的细胞周期进展较慢,对标准化疗的耐药性高于 MLL-AF9 细胞。这些表型主要由 ENL 的连接区和其中高度保守的赖氨酸残基 K469 控制。用乙酰化模拟谷氨酰胺取代 K469 可消除 MLL-ENL 抑制增殖和促进化疗耐药的能力。我们表明去乙酰化酶 Sirt2 可能作为 MLL-ENL 的上游调节剂。Sirt2 的缺失促进了具有 MLL 融合的 AML 细胞的增殖。重要的是,Sirt2 的缺失大大增强了 MLL-ENL AML 细胞对化疗的敏感性。总之,我们的研究揭示了 Sirt2 在白血病发生中的独特调节作用,并表明靶向 SIRT2 是提高 MLL-ENL AML 患者对化疗敏感性的新方法。