Kallioniemi Anne
Laboratory of Cancer Genetics, Tampere University Hospital and Institute of Medical Technology, University of Tampere, Biokatu 6, Tampere FI-33014, Finland.
Curr Opin Biotechnol. 2008 Feb;19(1):36-40. doi: 10.1016/j.copbio.2007.11.004. Epub 2007 Dec 26.
Genetic alterations are a key feature of cancer cells and typically target biological processes and pathways that contribute to cancer pathogenesis. Array-based comparative genomic hybridization (aCGH) has provided a wealth of new information on copy number changes in cancer on a genome-wide level and aCGH data have also been utilized in cancer classification. More importantly, aCGH analyses have allowed highly accurate localization of specific genetic alterations that, for example, are associated with tumor progression, therapy response, or patient outcome. The genes involved in these aberrations are likely to contribute to cancer pathogenesis, and the high-resolution mapping by aCGH greatly facilitates the subsequent identification of these cancer-associated genes.
基因改变是癌细胞的一个关键特征,通常针对有助于癌症发病机制的生物学过程和途径。基于阵列的比较基因组杂交(aCGH)在全基因组水平上提供了大量有关癌症拷贝数变化的新信息,并且aCGH数据也已用于癌症分类。更重要的是,aCGH分析能够高度准确地定位特定的基因改变,例如与肿瘤进展、治疗反应或患者预后相关的改变。参与这些畸变的基因可能有助于癌症发病机制,而aCGH的高分辨率图谱极大地促进了随后对这些癌症相关基因的鉴定。