Suppr超能文献

RUNX3/p46失活促进皮肤T细胞淋巴瘤。

Inactivation of RUNX3/p46 Promotes Cutaneous T-Cell Lymphoma.

作者信息

Haider Ahmed, Steininger Anne, Ullmann Reinhard, Hummel Michael, Dimitrova Lora, Beyer Marc, Vandersee Staffan, Lenze Dido, Sterry Wolfram, Assaf Chalid, Möbs Markus

机构信息

Department of Dermatology, Charité - Universitaetsmedizin Berlin, Berlin, Germany.

Max Planck Institute for Molecular Genetics, Berlin, Germany.

出版信息

J Invest Dermatol. 2016 Nov;136(11):2287-2296. doi: 10.1016/j.jid.2016.05.126. Epub 2016 Jul 1.

Abstract

The key role of RUNX3 in physiological T-cell differentiation has been extensively documented. However, information on its relevance for the development of human T-cell lymphomas or leukemias is scarce. Here, we show that alterations of RUNX3 by either heterozygous deletion or methylation of its distal promoter can be observed in the tumor cells of 15 of 21 (71%) patients suffering from Sézary syndrome, an aggressive variant of cutaneous T-cell lymphoma. As a consequence, mRNA levels of RUNX3/p46, the isoform controlled by the distal promoter, are significantly lower in Sézary syndrome tumor cells. Re-expression of RUNX3/p46 reduces cell viability and promotes apoptosis in a RUNX3/p46 cell line of cutaneous T-cell lymphoma. Based on this, we present evidence that RUNX3 can act as a tumor suppressor in a human T-cell malignancy and suggest that this effect is predominantly mediated through transcripts from its distal promoter, in particular RUNX3/p46.

摘要

RUNX3在生理性T细胞分化中的关键作用已得到广泛记载。然而,关于其与人类T细胞淋巴瘤或白血病发生发展相关性的信息却很匮乏。在此,我们发现,在21例患有蕈样肉芽肿综合征(一种侵袭性皮肤T细胞淋巴瘤变体)患者中的15例(71%)肿瘤细胞中,可观察到RUNX3因杂合性缺失或其远端启动子甲基化而发生改变。因此,由远端启动子控制的异构体RUNX3/p46的mRNA水平在蕈样肉芽肿综合征肿瘤细胞中显著降低。RUNX3/p46的重新表达降低了皮肤T细胞淋巴瘤RUNX3/p46细胞系中的细胞活力并促进细胞凋亡。基于此,我们提供证据表明RUNX3在人类T细胞恶性肿瘤中可作为一种肿瘤抑制因子,并表明这种效应主要通过其远端启动子的转录本介导,尤其是RUNX3/p46。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验