UCL School of Medicine, Cancer Institute, Academic Haematology, Royal Free Campus, Rowland Hill Street, Hampstead, London NW3 2PF, UK.
BMC Genomics. 2010 Jan 18;11:41. doi: 10.1186/1471-2164-11-41.
Chronic myelogenous leukemia (CML) results from the neoplastic transformation of a haematopoietic stem cell. The hallmark genetic abnormality of CML is a chimeric BCR/ABL1 fusion gene resulting from the Philadelphia chromosome rearrangement t(9;22)(q34;q11). Clinical and laboratory studies indicate that the BCR/ABL1 fusion protein is essential for initiation, maintenance and progression of CML, yet the event(s) driving the transformation from chronic phase to blast phase are poorly understood.
Here we report multiple genome aberrations in a collection of 78 CML and 14 control samples by oligonucleotide array comparative genomic hybridization. We found a unique signature of genome deletions within the immunoglobulin heavy chain (IGH) and T cell receptor regions (TCR), frequently accompanied by concomitant loss of sequences within the short arm regions of chromosomes 7 and 9, including IKZF1, HOXA7, CDKN2A/2B, MLLT3, IFNA/B, RNF38, PAX5, JMJD2C and PDCD1LG2 genes.
None of these genome losses were detected in any of the CML samples with myeloid transformation, chronic phase or controls, indicating that their presence is obligatory for the development of a malignant clone with a lymphoid phenotype. Notably, the coincidental deletions at IGH and TCR regions appear to precede the loss of IKZF1 and/or p16 genes in CML indicating a possible involvement of RAG in these deletions.
慢性髓细胞白血病(CML)是由造血干细胞的肿瘤转化引起的。CML 的标志性遗传异常是费城染色体重排 t(9;22)(q34;q11)导致的嵌合 BCR/ABL1 融合基因。临床和实验室研究表明,BCR/ABL1 融合蛋白对于 CML 的起始、维持和进展是必不可少的,但驱动从慢性期向急变期转变的事件尚不清楚。
我们通过寡核苷酸微阵列比较基因组杂交在 78 例 CML 和 14 例对照样本中报告了多个基因组异常。我们发现 IGH 和 TCR 区域内的免疫球蛋白重链(IGH)和 T 细胞受体区域(TCR)内存在独特的基因组缺失特征,经常伴有 7 号和 9 号染色体短臂区域内序列的同时缺失,包括 IKZF1、HOXA7、CDKN2A/2B、MLLT3、IFNA/B、RNF38、PAX5、JMJD2C 和 PDCD1LG2 基因。
在任何具有髓系转化、慢性期或对照的 CML 样本中均未检测到这些基因组缺失,表明其存在对于具有淋巴样表型的恶性克隆的发展是必需的。值得注意的是,IGH 和 TCR 区域的巧合缺失似乎先于 CML 中 IKZF1 和/或 p16 基因的缺失,表明 RAG 可能参与了这些缺失。