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组蛋白去甲基化酶 LSD1 最短异构体的过表达使造血干细胞恶性转化。

Overexpression of the shortest isoform of histone demethylase LSD1 primes hematopoietic stem cells for malignant transformation.

机构信息

Division of Stem Cell Regulation, Center for Molecular Medicine, Jichi Medical University, Tochigi, Japan; and.

Department of Disease Model, Research Institute for Radiation Biology and Medicine, Hiroshima University, Hiroshima, Japan.

出版信息

Blood. 2015 Jun 11;125(24):3731-46. doi: 10.1182/blood-2014-11-610907. Epub 2015 Apr 22.

Abstract

Recent investigations indicate that epigenetic regulators act at the initial step of myeloid leukemogenesis by forming preleukemic hematopoietic stem cells (HSCs), which possess the increased self-renewal potential but retain multidifferentiation ability, and synergize with genetic abnormalities in later stages to develop full-blown acute myeloid leukemias. However, it is still unknown whether this theory is applicable to other malignancies. In this study, we demonstrate that lysine-specific demethylase 1 (LSD1) overexpression is a founder abnormality for the development of T-cell lymphoblastic leukemia/lymphoma (T-LBL) using LSD1 transgenic mice. LSD1 expression is tightly regulated via alternative splicing and transcriptional repression in HSCs and is altered in most leukemias, especially T-LBL. Overexpression of the shortest isoform of LSD1, which is specifically repressed in quiescent HSCs and demethylates histone H3K9 more efficiently than other isoforms, increases self-renewal potential via upregulation of the HoxA family but retains multidifferentiation ability with a skewed differentiation to T-cell lineages at transcriptome levels in HSCs. Transgenic mice overexpressing LSD1 in HSCs did not show obvious abnormalities but developed T-LBL at very high frequency after γ-irradiation. LSD1 overexpression appears to be the first hit in T-cell leukemogenesis and provides an insight into novel strategies for early diagnosis and effective treatment of the disease.

摘要

最近的研究表明,表观遗传调节剂通过形成具有更高自我更新潜力但保留多向分化能力的前白血病造血干细胞(HSCs),在髓系白血病发生的初始步骤中发挥作用,并且与遗传异常在后期协同作用,发展为完全性急性髓系白血病。然而,目前尚不清楚这一理论是否适用于其他恶性肿瘤。在这项研究中,我们使用 LSD1 转基因小鼠证明,赖氨酸特异性去甲基酶 1(LSD1)的过表达是 T 细胞淋巴母细胞白血病/淋巴瘤(T-LBL)发展的起始异常。LSD1 的表达在 HSCs 中通过选择性剪接和转录抑制来严格调控,并且在大多数白血病中,特别是 T-LBL 中发生改变。最短的 LSD1 异构体的过表达,其在静止的 HSCs 中被特异性抑制,并且比其他异构体更有效地去甲基化组蛋白 H3K9,通过上调 HoxA 家族增加自我更新潜力,但在转录组水平上保持多向分化能力,向 T 细胞谱系分化偏倚。在 HSCs 中过表达 LSD1 的转基因小鼠没有表现出明显的异常,但在 γ 射线照射后非常高的频率发展为 T-LBL。LSD1 的过表达似乎是 T 细胞白血病发生的第一个打击,并为该疾病的早期诊断和有效治疗提供了新的策略。

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