Chan W C, Huang J Z
Department of Pathology and Microbiology, University of Nebraska Medical Center, USA.
Ann Hematol. 2001;80 Suppl 3:B38-41. doi: 10.1007/pl00022786.
The mRNA expression profile of a tumor reflects the unique genetic alterations present and is predictive of the clinical and biological characteristics of the tumor. Novel techniques have been developed to determine the global gene expression pattern of normal and neoplastic tissues. A cDNA microarray uniquely suitable for the analysis of B-cell non-Hodgkin's lymphomas (B-NHL) has been developed and preliminary analysis on diffuse large B-cell lymphoma (DLBCL), follicular lymphoma (FL) and B-chronic lymphocytic leukemia (CLL) has been performed. These studies indicate that: 1) it is feasible to determine the gene expression profiles of archival lymphoma samples frozen and stored in a clinical setting, 2) the expression profile of these 3 types of lymphoproliferative disorders are distinctive, 3) DLBCL can be divided into at least 2 major subgroups according to their pattern of expression of B-cell associated genes and 4) the gene expression patterns in DLBCL appear to have prognostic significance. A larger study of DLBCL is currently underway to confirm and extend our findings. Gene expression profiles will be correlated with cytogenetic and clinical data to identify distinctive profiles that are of clinical and biological significance and to delineate key genetic lesions that determine these profiles. The new information will allow the design of a simpler and less expensive array for clinical use. The diagnostic array could provide rapid molecular characterization of every B-NHL at presentation for optimal treatment decisions and prognostication. It is anticipated that this project will advance our understanding of the molecular mechanisms in the neoplastic transformation of B-lymphoid cells and the new insights will help to identify promising molecular targets for therapeutic intervention.
肿瘤的信使核糖核酸(mRNA)表达谱反映了其存在的独特基因改变,并可预测肿瘤的临床和生物学特征。已开发出新技术来确定正常组织和肿瘤组织的整体基因表达模式。一种特别适用于分析B细胞非霍奇金淋巴瘤(B-NHL)的互补脱氧核糖核酸(cDNA)微阵列已被开发出来,并已对弥漫性大B细胞淋巴瘤(DLBCL)、滤泡性淋巴瘤(FL)和B细胞慢性淋巴细胞白血病(CLL)进行了初步分析。这些研究表明:1)确定在临床环境中冷冻保存的存档淋巴瘤样本的基因表达谱是可行的;2)这三种类型的淋巴增殖性疾病的表达谱是独特的;3)根据B细胞相关基因的表达模式,DLBCL可至少分为两个主要亚组;4)DLBCL中的基因表达模式似乎具有预后意义。目前正在对DLBCL进行更大规模的研究,以证实和扩展我们的发现。基因表达谱将与细胞遗传学和临床数据相关联,以识别具有临床和生物学意义的独特谱,并描绘决定这些谱的关键基因损伤。这些新信息将有助于设计一种更简单、成本更低的用于临床的阵列。诊断阵列可为每个初诊的B-NHL提供快速分子特征分析,以做出最佳治疗决策和进行预后评估。预计该项目将增进我们对B淋巴细胞肿瘤转化分子机制的理解,这些新见解将有助于识别有前景的治疗干预分子靶点。