Dybkaer Karen, Iqbal Javeed, Zhou Guimei, Chan Wing C
Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, 68198, USA.
Clin Lymphoma. 2004 Jun;5(1):19-28. doi: 10.3816/clm.2004.n.006.
Lymphoid malignancies are grouped and characterized by their morphology, immunophenotype, and genetic aberrations to help establish a diagnosis. Use of microarray technology enables the simultaneous determination of expression levels for thousands of genes, providing an additional powerful tool for improving disease classification. In this review, recent studies of diffuse large B-cell lymphoma (DLBCL), primary mediastinal large B-cell lymphoma, mantle cell lymphoma (MCL), and follicular lymphoma are highlighted, and the impact of gene expression profiling on the molecular diagnosis of these diseases is discussed. Based on microarray-generated gene expression profiles, outcome predictors were constructed for DLBCL and MCL. Specific expression patterns of a limited number of genes at the time of diagnosis were linked to overall survival in DLBCL and MCL. Such predictors of prognosis may eventually lead to risk-adjusted treatment of lymphomas. Specific therapeutic targets may also emerge with increased insight into the molecular features of the different lymphomas, thus illustrating the usefulness of gene expression profiling not only to improve diagnosis and classification but also to generate prognostic indicators and targets for therapy.
淋巴系统恶性肿瘤根据其形态学、免疫表型和基因畸变进行分类和特征描述,以协助诊断。微阵列技术的应用能够同时测定数千个基因的表达水平,为改进疾病分类提供了又一强大工具。在本综述中,重点介绍了弥漫性大B细胞淋巴瘤(DLBCL)、原发性纵隔大B细胞淋巴瘤、套细胞淋巴瘤(MCL)和滤泡性淋巴瘤的近期研究,并讨论了基因表达谱分析对这些疾病分子诊断的影响。基于微阵列产生的基因表达谱,构建了DLBCL和MCL的预后预测指标。诊断时少数基因的特定表达模式与DLBCL和MCL的总生存期相关。此类预后预测指标最终可能会带来淋巴瘤的风险调整治疗。随着对不同淋巴瘤分子特征的深入了解,也可能会出现特定的治疗靶点,从而说明基因表达谱分析不仅有助于改进诊断和分类,还能生成预后指标和治疗靶点。