Department of Biological Sciences, Sookmyung Women's University, Seoul 140-742, Korea.
BMB Rep. 2013 Feb;46(2):97-102. doi: 10.5483/bmbrep.2013.46.2.226.
The use of various cancer cell lines can recapitulate known tumor-associated mutations and genetically define cancer subsets. This approach also enables comparative surveys of associations between cancer mutations and drug responses. Here, we analyzed the effects of ~40,000 compounds on cancer cell lines that showed diverse mutation-dependent sensitivity profiles. Over 1,000 compounds exhibited unique sensitivity on cell lines with specific mutational genotypes, and these compounds were clustered into six different classes of mutation-oriented sensitivity. The present analysis provides new insights into the relationship between somatic mutations and selectivity response of chemicals, and these results should have applications related to predicting and optimizing therapeutic windows for anti-cancer agents.
使用各种癌细胞系可以重现已知的肿瘤相关突变,并从遗传学上定义癌症亚群。这种方法还可以比较调查癌症突变与药物反应之间的关联。在这里,我们分析了约 40000 种化合物对表现出不同突变依赖性敏感性谱的癌细胞系的影响。超过 1000 种化合物在具有特定突变基因型的细胞系上表现出独特的敏感性,这些化合物被分为六种不同的突变定向敏感性类别。本分析提供了关于体细胞突变与化学物质选择性反应之间关系的新见解,这些结果应该与预测和优化抗癌药物的治疗窗口有关。