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HOXA9/IRX1 表达模式定义了婴儿 MLL-AF4 驱动的急性淋巴细胞白血病的两个亚群。

HOXA9/IRX1 expression pattern defines two subgroups of infant MLL-AF4-driven acute lymphoblastic leukemia.

机构信息

Centre for Regenerative Medicine, Institute for Regeneration and Repair, University of Edinburgh, Edinburgh, UK.

Centre for Regenerative Medicine, Institute for Regeneration and Repair, University of Edinburgh, Edinburgh, UK.

出版信息

Exp Hematol. 2021 Jan;93:38-43.e5. doi: 10.1016/j.exphem.2020.10.002. Epub 2020 Oct 15.

DOI:10.1016/j.exphem.2020.10.002
PMID:33069783
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7851112/
Abstract

Infant t(4;11) acute lymphoblastic leukemia is the most common leukemia in infant patients and has a highly aggressive nature. The patients have a dismal prognosis, which has not improved in more than a decade, suggesting that a better understanding of this disease is required. In the study described here, we analyzed two previously published RNA-sequencing data sets and gained further insights into the global transcriptomes of two known subgroups of this disease, which are characterized by the presence or absence of a homeobox gene expression signature. Specifically, we identified a remarkable mutually exclusive expression of the HOXA9/HOXA10 and IRX1 genes and termed the two subgroups iALL-HOXA9 and iALL-IRX1. This expression pattern is critical as it suggests that there is a fundamental difference between the two subgroups. Investigation of the transcriptomes of the two subgroups reveals a more aggressive nature for the iALL-IRX1 group, which is further supported by the fact that patients within this group have a worse prognosis and are also diagnosed at a younger age. This could be reflective of a developmentally earlier cell of origin for iALL-IRX1. Our analysis further uncovered critical differences between the two groups that may have an impact on treatment strategies. In summary, after a detailed investigation into the transcriptional profiles of iALL-HOXA9 and iALL-IRX1 patients, we highlight the importance of acknowledging that these two subgroups are different and that this is of clinical importance.

摘要

婴儿 t(4;11) 急性淋巴细胞白血病是婴儿患者中最常见的白血病,具有高度侵袭性。患者预后极差,十多年来没有改善,这表明需要更好地了解这种疾病。在本文描述的研究中,我们分析了两个先前发表的 RNA 测序数据集,并进一步深入了解了这种疾病两个已知亚组的全球转录组,这两个亚组的特征是存在或不存在同源盒基因表达特征。具体来说,我们鉴定了 HOXA9/HOXA10 和 IRX1 基因的显著互斥表达,并将这两个亚组分别命名为 iALL-HOXA9 和 iALL-IRX1。这种表达模式非常重要,因为它表明这两个亚组之间存在根本差异。对这两个亚组的转录组的研究揭示了 iALL-IRX1 组的更具侵袭性的性质,这进一步得到了以下事实的支持:该组的患者预后更差,并且也被诊断为更年轻。这可能反映了 iALL-IRX1 的起源细胞在发育上更早。我们的分析还揭示了两组之间可能对治疗策略产生影响的关键差异。总之,在对 iALL-HOXA9 和 iALL-IRX1 患者的转录谱进行详细调查后,我们强调了承认这两个亚组不同的重要性,这具有临床意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7310/7851112/be656fe248b0/gr7.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7310/7851112/76c64416d2e7/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7310/7851112/7cf8d8f3b4d7/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7310/7851112/8cc7a23c8cd8/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7310/7851112/202275b6072d/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7310/7851112/b097738b067b/gr5.jpg
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