Fu Kai, Weisenburger Dennis D, Greiner Timothy C, Dave Sandeep, Wright George, Rosenwald Andreas, Chiorazzi Michael, Iqbal Javeed, Gesk Stefan, Siebert Reiner, De Jong Daphne, Jaffe Elaine S, Wilson Wyndham H, Delabie Jan, Ott German, Dave Bhavana J, Sanger Warren G, Smith Lynette M, Rimsza Lisa, Braziel Rita M, Müller-Hermelink H Konrad, Campo Elias, Gascoyne Randy D, Staudt Louis M, Chan Wing C
Department of Pathology and Microbiology, University of Nebraska Medical Center, 983135 Nebraska Medical Center, Omaha, NE 68198-3135, USA.
Blood. 2005 Dec 15;106(13):4315-21. doi: 10.1182/blood-2005-04-1753. Epub 2005 Aug 25.
Cyclin D1 overexpression is believed to be essential in the pathogenesis of mantle cell lymphoma (MCL). Hence, the existence of cyclin D1-negative MCL has been controversial and difficult to substantiate. Our previous gene expression profiling study identified several cases that lacked cyclin D1 expression, but had a gene expression signature typical of MCL. Herein, we report the clinical, pathologic, and genetic features of 6 cases of cyclin D1-negative MCL. All 6 cases exhibited the characteristic morphologic features and the unique gene expression signature of MCL but lacked the t(11;14)(q13; q32) by fluorescence in situ hybridization (FISH) analysis. The tumor cells also failed to express cyclin D1 protein, but instead expressed either cyclin D2 (2 cases) or cyclin D3 (4 cases). There was good correlation between cyclin D protein expression and the corresponding mRNA expression levels by gene expression analysis. Using interphase FISH, we did not detect chromosomal translocations or amplifications involving CCND2 and CCND3 loci in these cases. Patients with cyclin D1-negative MCL were similar clinically to those with cyclin D1-positive MCL. In conclusion, cases of cyclin D1-negative MCL do exist and are part of the spectrum of MCL. Up-regulation of cyclin D2 or D3 may substitute for cyclin D1 in the pathogenesis of MCL.
细胞周期蛋白D1过表达被认为在套细胞淋巴瘤(MCL)的发病机制中至关重要。因此,细胞周期蛋白D1阴性的MCL的存在一直存在争议且难以证实。我们之前的基因表达谱研究确定了几例缺乏细胞周期蛋白D1表达但具有MCL典型基因表达特征的病例。在此,我们报告6例细胞周期蛋白D1阴性MCL的临床、病理和遗传学特征。所有6例均表现出MCL的特征性形态学特征和独特的基因表达特征,但荧光原位杂交(FISH)分析未发现t(11;14)(q13;q32)。肿瘤细胞也未表达细胞周期蛋白D1蛋白,而是表达细胞周期蛋白D2(2例)或细胞周期蛋白D3(4例)。通过基因表达分析,细胞周期蛋白D蛋白表达与相应的mRNA表达水平之间存在良好的相关性。在这些病例中,使用间期FISH我们未检测到涉及CCND2和CCND3基因座的染色体易位或扩增。细胞周期蛋白D1阴性MCL患者在临床上与细胞周期蛋白D1阳性MCL患者相似。总之,细胞周期蛋白D1阴性的MCL病例确实存在,并且是MCL谱系的一部分。在MCL的发病机制中,细胞周期蛋白D2或D3的上调可能替代细胞周期蛋白D1。