Chang Hong, Yeung Joanna, Xu Wei, Ning Yi, Patterson Bruce
Department of Laboratory Hematology, University Health Network, University of Toronto, Toronto, ON, Canada.
Br J Haematol. 2006 Sep;134(6):613-5. doi: 10.1111/j.1365-2141.2006.06237.x. Epub 2006 Aug 1.
The genetic events that lead to tumour progression in plasma cell dyscrasia are not well understood. Interphase cytoplasmic fluorescence in situ hybridisation was used to investigate the CKS1B amplification status (at 1q21) in clonal plasma cells from 123 patients: 23 monoclonal gammopathy of undetermined significance (MGUS), 75 multiple myeloma (MM) and 26 plasma cell leukaemia (PCL). While CKS1B amplification was absent in MGUS patients, such amplification (3-8 copies) was detected in 36% of newly diagnosed MM, 52% relapsed MM and 62% PCL (P < 0.001). Our results suggest that CKS1B amplification is associated with transformation from MGUS to MM and progression to PCL.
导致浆细胞发育异常中肿瘤进展的遗传事件尚未完全明确。运用间期细胞质荧光原位杂交技术,对123例患者的克隆性浆细胞中CKS1B基因(位于1q21)的扩增状态进行了研究,其中包括23例意义未明的单克隆丙种球蛋白病(MGUS)、75例多发性骨髓瘤(MM)和26例浆细胞白血病(PCL)。MGUS患者未检测到CKS1B基因扩增,而在36%的新诊断MM、52%的复发MM以及62%的PCL患者中检测到了该基因扩增(3 - 8个拷贝,P < 0.001)。我们的研究结果表明,CKS1B基因扩增与MGUS向MM的转化以及向PCL的进展相关。