Staunton J E, Slonim D K, Coller H A, Tamayo P, Angelo M J, Park J, Scherf U, Lee J K, Reinhold W O, Weinstein J N, Mesirov J P, Lander E S, Golub T R
Whitehead/Massachusetts Institute of Technology Center for Genome Research, Cambridge, MA 02139, USA.
Proc Natl Acad Sci U S A. 2001 Sep 11;98(19):10787-92. doi: 10.1073/pnas.191368598.
In an effort to develop a genomics-based approach to the prediction of drug response, we have developed an algorithm for classification of cell line chemosensitivity based on gene expression profiles alone. Using oligonucleotide microarrays, the expression levels of 6,817 genes were measured in a panel of 60 human cancer cell lines (the NCI-60) for which the chemosensitivity profiles of thousands of chemical compounds have been determined. We sought to determine whether the gene expression signatures of untreated cells were sufficient for the prediction of chemosensitivity. Gene expression-based classifiers of sensitivity or resistance for 232 compounds were generated and then evaluated on independent sets of data. The classifiers were designed to be independent of the cells' tissue of origin. The accuracy of chemosensitivity prediction was considerably better than would be expected by chance. Eighty-eight of 232 expression-based classifiers performed accurately (with P < 0.05) on an independent test set, whereas only 12 of the 232 would be expected to do so by chance. These results suggest that at least for a subset of compounds genomic approaches to chemosensitivity prediction are feasible.
为了开发一种基于基因组学的药物反应预测方法,我们仅基于基因表达谱开发了一种细胞系化学敏感性分类算法。使用寡核苷酸微阵列,在一组60个人类癌细胞系(NCI-60)中测量了6817个基因的表达水平,对于这些细胞系,已经确定了数千种化合物的化学敏感性谱。我们试图确定未处理细胞的基因表达特征是否足以预测化学敏感性。生成了基于基因表达的232种化合物敏感性或抗性分类器,然后在独立数据集上进行评估。这些分类器设计为独立于细胞的起源组织。化学敏感性预测的准确性比随机预期的要好得多。232个基于表达的分类器中有88个在独立测试集上表现准确(P < 0.05),而232个中随机预期只有12个会如此。这些结果表明,至少对于一部分化合物,基于基因组学的化学敏感性预测方法是可行的。