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Tet1 并非新型小鼠模型中 MLL-ENL 诱导髓系白血病所必需的。

Tet1 is not required for myeloid leukemogenesis by MLL-ENL in novel mouse models.

机构信息

Department of Microbiology and Molecular Genetics, Mie University Graduate School of Medicine, Tsu, Mie, Japan.

Department of Hematology and Oncology, Mie University Graduate School of Medicine, Tsu, Mie, Japan.

出版信息

PLoS One. 2021 Mar 11;16(3):e0248425. doi: 10.1371/journal.pone.0248425. eCollection 2021.

Abstract

The Ten Eleven Translocation 1 (TET1) gene encodes an epigenetic modifying molecule that is involved in demethylation of 5-methylcytosine. In hematological malignancies, loss-of-function mutations of TET2, which is one of the TET family genes including TET1, are frequently found, while the mutations of TET1 are not. However, clinical studies have revealed that TET1 is highly expressed in some cases of the hematological malignancies including acute myeloid leukemia. Indeed, studies by mouse models using conventional Tet1 knockout mice demonstrated that Tet1 is involved in myeloid leukemogenesis by Mixed Lineage Leukemia (MLL) fusion gene or TET2 mutant. Meanwhile, the other study showed that Tet1 is highly expressed in hematopoietic stem cells (HSCs), and that deletion of Tet1 in HSCs enhances potential self-renewal capacity, which is potentially associated with myeloid leukemogenesis. To examine the role of Tet1 in myeloid leukemogenesis more precisely, we generated novel conditional Tet1-knockout mice, which were used to generate the compound mutant mice by crossing with the inducible MLL-ENL transgenic mice that we developed previously. The leukemic immortalization in vitro was not critically affected by conditional ablation of Tet1 in HSCs with the induced expression of MLL-ENL or in hematopoietic progenitor cells retrovirally transduced with MLL-ENL. In addition, the leukemic phenotypes caused by the induced expression of MLL-ENL in vivo was not also critically affected in the compound mutant mouse model by conditional ablation of Tet1, although we found that the expression of Evi1, which is one of critical target genes of MLL fusion gene, in tumor cells was remarkably low under Tet1-ablated condition. These results revealed that Tet1 was dispensable for the myeloid leukemogenesis by MLL-ENL, suggesting that the therapeutic application of Tet1 inhibition may need careful assessment.

摘要

TET1 基因易位 1(TET1)基因编码一种表观遗传修饰分子,参与 5-甲基胞嘧啶的去甲基化。在血液恶性肿瘤中,TET2 是 TET 家族基因之一,其功能丧失突变频繁发生,而 TET1 突变则不常见。然而,临床研究表明,TET1 在某些血液恶性肿瘤中高度表达,包括急性髓系白血病。事实上,使用常规 Tet1 敲除小鼠的小鼠模型研究表明,Tet1 通过混合谱系白血病(MLL)融合基因或 TET2 突变参与髓系白血病发生。同时,另一项研究表明,Tet1 在造血干细胞(HSCs)中高度表达,并且 HSCs 中 Tet1 的缺失增强了潜在的自我更新能力,这可能与髓系白血病发生有关。为了更精确地研究 Tet1 在髓系白血病发生中的作用,我们生成了新型条件性 Tet1 敲除小鼠,并将其与我们先前开发的诱导型 MLL-ENL 转基因小鼠进行杂交,以生成复合突变小鼠。在体外,当 MLL-ENL 诱导表达或逆转录病毒转导的造血祖细胞中 Tet1 条件性缺失时,白血病的永生化并未受到严重影响。此外,当 MLL-ENL 在体内诱导表达时,在条件性缺失 Tet1 的复合突变小鼠模型中,白血病表型也没有受到严重影响,尽管我们发现,在 Tet1 缺失条件下,肿瘤细胞中 MLL 融合基因的一个关键靶基因 Evi1 的表达显著降低。这些结果表明,Tet1 对于 MLL-ENL 诱导的髓系白血病发生不是必需的,提示 Tet1 抑制的治疗应用可能需要仔细评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/236c/7951824/ec14f01a4876/pone.0248425.g001.jpg

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