Haider Ahmed, Steininger Anne, Ullmann Reinhard, Hummel Michael, Dimitrova Lora, Beyer Marc, Vandersee Staffan, Lenze Dido, Sterry Wolfram, Assaf Chalid, Möbs Markus
Department of Dermatology, Charité - Universitaetsmedizin Berlin, Berlin, Germany.
Max Planck Institute for Molecular Genetics, Berlin, Germany.
J Invest Dermatol. 2016 Nov;136(11):2287-2296. doi: 10.1016/j.jid.2016.05.126. Epub 2016 Jul 1.
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.
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。