Van Vlierberghe Pieter, van Grotel Martine, Tchinda Joëlle, Lee Charles, Beverloo H Berna, van der Spek Peter J, Stubbs Andrew, Cools Jan, Nagata Kyosuke, Fornerod Maarten, Buijs-Gladdines Jessica, Horstmann Martin, van Wering Elisabeth R, Soulier Jean, Pieters Rob, Meijerink Jules P P
Department of Pediatric Oncology/Hematology, Erasmus Medical Center Sophia Children's Hospital, Rotterdam, The Netherlands.
Blood. 2008 May 1;111(9):4668-80. doi: 10.1182/blood-2007-09-111872. Epub 2008 Feb 25.
T-cell acute lymphoblastic leukemia (T-ALL) is mostly characterized by specific chromosomal abnormalities, some occurring in a mutually exclusive manner that possibly delineate specific T-ALL subgroups. One subgroup, including MLL-rearranged, CALM-AF10 or inv (7)(p15q34) patients, is characterized by elevated expression of HOXA genes. Using a gene expression-based clustering analysis of 67 T-ALL cases with recurrent molecular genetic abnormalities and 25 samples lacking apparent aberrations, we identified 5 new patients with elevated HOXA levels. Using microarray-based comparative genomic hybridization (array-CGH), a cryptic and recurrent deletion, del (9)(q34.11q34.13), was exclusively identified in 3 of these 5 patients. This deletion results in a conserved SET-NUP214 fusion product, which was also identified in the T-ALL cell line LOUCY. SET-NUP214 binds in the promoter regions of specific HOXA genes, where it interacts with CRM1 and DOT1L, which may transcriptionally activate specific members of the HOXA cluster. Targeted inhibition of SET-NUP214 by siRNA abolished expression of HOXA genes, inhibited proliferation, and induced differentiation in LOUCY but not in other T-ALL lines. We conclude that SET-NUP214 may contribute to the pathogenesis of T-ALL by enforcing T-cell differentiation arrest.
T细胞急性淋巴细胞白血病(T-ALL)大多具有特定的染色体异常特征,其中一些以相互排斥的方式出现,这可能界定了特定的T-ALL亚组。一个亚组,包括MLL重排、CALM-AF10或inv(7)(p15q34)患者,其特征是HOXA基因表达升高。通过对67例具有复发性分子遗传异常的T-ALL病例和25例无明显畸变的样本进行基于基因表达的聚类分析,我们鉴定出5例HOXA水平升高的新患者。使用基于微阵列的比较基因组杂交(阵列CGH),在这5例患者中的3例中专门鉴定出一种隐匿性和复发性缺失,即del(9)(q34.11q34.13)。这种缺失产生一种保守的SET-NUP214融合产物,在T-ALL细胞系LOUCY中也被鉴定出来。SET-NUP214结合在特定HOXA基因的启动子区域,在那里它与CRM1和DOT1L相互作用,这可能转录激活HOXA簇的特定成员。用小干扰RNA(siRNA)靶向抑制SET-NUP214可消除HOXA基因的表达,抑制LOUCY细胞的增殖并诱导其分化,但对其他T-ALL细胞系无此作用。我们得出结论,SET-NUP214可能通过导致T细胞分化停滞而促进T-ALL的发病机制。