Plass Christoph, Byrd John C, Raval Aparna, Tanner Stephan M, de la Chapelle Albert
Department of Molecular Virology, Immunology, and Medical Genetics, Human Cancer Genetics Program, the Comprehensive Cancer Center at the Ohio State University, Columbus, OH, USA.
Br J Haematol. 2007 Dec;139(5):744-52. doi: 10.1111/j.1365-2141.2007.06875.x. Epub 2007 Oct 24.
Molecular profiling may lead to a better understanding of a disease. This knowledge is especially important in malignancies, where multiple alterations are required during the progression from premalignant to malignant stages. Such information can be useful for the development of novel biomarkers that allow the prediction of a clinical course, response to treatment or early detection. Molecular data is also utilized to develop targeted therapies. Moreover, gene defects identified in profiling studies will help to understand the molecular pathways disrupted in the disease. This review provides an overview of molecular profiling approaches in chronic lymphocytic leukaemia (CLL). We will describe our current understanding of genetic alterations in CLL, the use of familial CLL for the identification of predisposing mutations, and the search for epigenetic alterations in CLL.
分子谱分析可能有助于更好地理解疾病。这一知识在恶性肿瘤中尤为重要,因为从癌前阶段发展到恶性阶段需要多种改变。此类信息对于开发能够预测临床病程、治疗反应或早期检测的新型生物标志物可能有用。分子数据还被用于开发靶向治疗。此外,在谱分析研究中鉴定出的基因缺陷将有助于理解疾病中被破坏的分子途径。本综述概述了慢性淋巴细胞白血病(CLL)的分子谱分析方法。我们将描述目前对CLL基因改变的理解、利用家族性CLL鉴定易感突变,以及寻找CLL中的表观遗传改变。