Pediatric Hematology-Oncology Program, Research Center, Instituto Nacional de Câncer, Rio de Janeiro, Brazil.
Cancer Lett. 2013 May 10;332(1):30-4. doi: 10.1016/j.canlet.2012.12.023. Epub 2013 Jan 20.
MLL gene aberrations are frequently diagnosed in infant acute myeloid leukemia (AML). We previously described the MLL-NEBL and NEBL-MLL genomic fusions in an infant AML patient with a chromosomal translocation t(10;11)(p12;q23). NEBL was the second Nebulin family member (LASP1, NEBL) which was found to be involved in MLL rearrangements. Here, we report on our attempts to unravel the oncogenic properties of both fusion genes. First, RT-PCR analyses revealed the presence of the MLL-NEBL and NEBL-MLL mRNAs in the diagnostic sample of the patient. Next, expression cassettes for MLL-NEBL and NEBL-MLL were cloned into a sleeping beauty vector backbone. After stable transfection, the biological effects of MLL-NEBL, NEBL-MLL or the combination of both fusion proteins were investigated in a conditional cell culture model. NEBL-MLL but also co-transfected cells displayed significantly higher growth rates according to the data obtained by cell proliferation assay. The focus formation experiments revealed differences in the shape and number of colonies when comparing MLL-NEBL, NEBL-MLL- and co-transfected cells. The results obtained in this study suggest that the reciprocal fusion genes of the Nebulin gene family might be of biological importance.
MLL 基因异常经常在婴儿急性髓系白血病(AML)中诊断出来。我们之前在一位患有染色体易位 t(10;11)(p12;q23)的婴儿 AML 患者中描述了 MLL-NEBL 和 NEBL-MLL 基因组融合。NEBL 是第二个被发现参与 MLL 重排的 Nebulin 家族成员(LASP1,NEBL)。在这里,我们报告了我们试图揭开这两个融合基因致癌性质的尝试。首先,RT-PCR 分析显示在患者的诊断样本中存在 MLL-NEBL 和 NEBL-MLL mRNAs。接下来,将 MLL-NEBL 和 NEBL-MLL 的表达盒克隆到睡眠美人载体骨架中。在稳定转染后,在条件细胞培养模型中研究了 MLL-NEBL、NEBL-MLL 或两种融合蛋白的组合的生物学效应。根据细胞增殖测定获得的数据,NEBL-MLL 甚至共转染的细胞显示出明显更高的生长速率。焦点形成实验显示比较 MLL-NEBL、NEBL-MLL 和共转染细胞时,在形状和菌落数量上存在差异。本研究的结果表明,Nebulin 基因家族的相互融合基因可能具有生物学重要性。