| Literature DB >> 27377697 |
Ahmed Haider1, Anne Steininger2, Reinhard Ullmann3, Michael Hummel4, Lora Dimitrova4, Marc Beyer1, Staffan Vandersee5, Dido Lenze4, Wolfram Sterry1, Chalid Assaf6, Markus Möbs7.
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/p46low 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.Entities:
Mesh:
Substances:
Year: 2016 PMID: 27377697 DOI: 10.1016/j.jid.2016.05.126
Source DB: PubMed Journal: J Invest Dermatol ISSN: 0022-202X Impact factor: 8.551