Chng Wee Joo, Van Wier Scott A, Ahmann Gregory J, Winkler Jerry M, Jalal Syed M, Bergsagel Peter Leif, Chesi Marta, Trendle Mike C, Oken Martin M, Blood Emily, Henderson Kim, Santana-Dávila Rafael, Kyle Robert A, Gertz Morie A, Lacy Martha Q, Dispenzieri Angela, Greipp Philip R, Fonseca Rafael
Mayo Clinic Scottsdale, Comprehensive Cancer Center and Division of Hematology and Onocology, Scottsdale, AZ 85259, USA.
Blood. 2005 Sep 15;106(6):2156-61. doi: 10.1182/blood-2005-02-0761. Epub 2005 May 26.
Two major genetic categories of multiple myeloma (MM) exist. Hyperdiploid MM (48 to 74 chromosomes, median 53 chromosomes) is associated with trisomies especially of chromosomes 3, 7, 9, 11, 15, and 19, whereas the nonhyperdiploid (< 48 chromosomes or more than 74 chromosomes) MM is associated with primary translocations such as t(11;14), t(4;14), and t(14;16). Whether this dichotomy exists in monoclonal gammopathy of undetermined significance (MGUS) is uncertain due to limitations of current methods in the study of ploidy. This is especially true in MGUS where the number of clonal plasma cells is small. In this study, we derived a fluorescent in situ hybridization (FISH)-based trisomy index from pooled cytogenetic data (karyotype analysis) from 2 large cohorts of patients with MM with abnormal karyotype, and then validated it in 2 independent cohorts of patients who had known ploidy status either by karyotyping or DNA content measurement using flow cytometry. Using the criteria of 2 or more trisomies from a 3-chromosome combination, hyperdiploid myeloma can be detected with high specificity. Applying this index on 28 patients with smoldering multiple myeloma (SMM) or MGUS (11 SMM, 17 MGUS) who had normal karyotype, 11 cases of hyperdiploid SMM/MGUS were detected. This percentage (40%) is remarkably similar to the percentage of hyperdiploid MM reported in the literature, suggesting that hyperdiploid MM may originate early during disease evolution.
多发性骨髓瘤(MM)存在两种主要的基因类别。超二倍体MM(48至74条染色体,中位数为53条染色体)与三体性相关,尤其是3号、7号、9号、11号、15号和19号染色体的三体性,而非超二倍体(<48条染色体或>74条染色体)MM与原发性易位相关,如t(11;14)、t(4;14)和t(14;16)。由于目前研究倍性的方法存在局限性,这种二分法在意义未明的单克隆丙种球蛋白病(MGUS)中是否存在尚不确定。在MGUS中尤其如此,因为克隆性浆细胞数量很少。在本研究中,我们从2个大型异常核型MM患者队列的汇总细胞遗传学数据(核型分析)中得出了基于荧光原位杂交(FISH)的三体指数,然后在2个独立队列中进行了验证,这些队列中的患者通过核型分析或使用流式细胞术测量DNA含量已知倍性状态。使用来自3染色体组合的2个或更多三体性的标准,可以高特异性地检测超二倍体骨髓瘤。将该指数应用于28例核型正常的冒烟型多发性骨髓瘤(SMM)或MGUS患者(11例SMM,17例MGUS),检测到11例超二倍体SMM/MGUS。这个百分比(40%)与文献中报道的超二倍体MM的百分比非常相似,表明超二倍体MM可能在疾病演变的早期就已出现。