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伴有不连续12q12 - 14扩增子增加的转化型弥漫性大B细胞淋巴瘤显示CDK2、CDK4和GADD153基因同时失调。

Transformed diffuse large B-cell lymphomas with gains of the discontinuous 12q12-14 amplicon display concurrent deregulation of CDK2, CDK4 and GADD153 genes.

作者信息

Al-Assar Osama, Rees-Unwin Karen S, Menasce Lia P, Hough Rachael E, Goepel John R, Hammond David W, Hancock Barry W

机构信息

Yorkshire Cancer Research Institute for Cancer Studies, Division of Genomic Medicine, University of Sheffield, Sheffield, UK.

出版信息

Br J Haematol. 2006 Jun;133(6):612-21. doi: 10.1111/j.1365-2141.2006.06093.x.

Abstract

Transformation of the indolent follicular lymphoma (FL) to the aggressive diffuse large B-cell lymphoma (DLBCL) results in resistance to therapy with shortened survival. It has been demonstrated that the 12q12-14 region was mainly amplified in DLBCL cases but not in their FL counterparts. Therefore, we examined the DNA copy number and protein expression profiles for CDK2, CDK4 and GADD153, three genes that map to 12q12-14, in a set of 44 paired FL/DLBCL samples from 22 patients. The concordant amplification of these genes occurred in seven of 22 (32%) of FL cases, compared with 15 of 22 (68%) of DLBCL cases. At the protein level, 15 of 22 of the DLBCL samples (68%) showed strong staining for the CDK2 protein, compared with five of 21 of FL samples (24%). The majority of the DLBCL samples (16/22, 72%) expressed the CDK4 protein, whereas the majority of the FL samples (12/21, 57%) showed no expression of this protein. Except for one DLBCL case, no expression of the GADD153 protein could be detected. The deregulation of the CDK2 and CDK4 genes at the genetic and protein levels suggest a functional role for these genes in the transformation process and could potentially provide targets for prognostic tests or therapeutic interventions.

摘要

惰性滤泡性淋巴瘤(FL)转化为侵袭性弥漫性大B细胞淋巴瘤(DLBCL)会导致对治疗产生耐药性,生存期缩短。已有研究表明,12q12 - 14区域主要在DLBCL病例中扩增,而在其对应的FL病例中未出现扩增。因此,我们检测了22例患者的44对FL/DLBCL样本中,定位于12q12 - 14区域的三个基因CDK2、CDK4和GADD153的DNA拷贝数及蛋白表达谱。这些基因的一致性扩增在22例FL病例中的7例(32%)出现,而在22例DLBCL病例中有15例(68%)出现。在蛋白水平上,22例DLBCL样本中有15例(68%)对CDK2蛋白呈强染色,而21例FL样本中只有5例(24%)如此。大多数DLBCL样本(16/22,72%)表达CDK4蛋白,而大多数FL样本(12/21,57%)未表达该蛋白。除1例DLBCL病例外,未检测到GADD153蛋白的表达。CDK2和CDK4基因在遗传和蛋白水平的失调表明这些基因在转化过程中发挥功能性作用,并可能为预后检测或治疗干预提供潜在靶点。

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