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合理化癌细胞系的药物反应。

Rationalizing Drug Response in Cancer Cell Lines.

机构信息

Joint IRB-BSC-CRG Program in Computational Biology, Institute for Research in Biomedicine (IRB Barcelona), The Barcelona Institute of Science and Technology, Barcelona, Catalonia, Spain.

Joint IRB-BSC-CRG Program in Computational Biology, Institute for Research in Biomedicine (IRB Barcelona), The Barcelona Institute of Science and Technology, Barcelona, Catalonia, Spain; Institució Catalana de Recerca i Estudis Avançats (ICREA), Barcelona, Catalonia, Spain.

出版信息

J Mol Biol. 2018 Sep 14;430(18 Pt A):3016-3027. doi: 10.1016/j.jmb.2018.03.021. Epub 2018 Apr 4.

Abstract

Cancer cell lines (CCLs) play an important role in the initial stages of drug discovery allowing, among others, for the screening of drug candidates. As CCL panels continue to grow in size and diversity, many polymorphisms in genes encoding drug-metabolizing enzymes, transporters and drug targets, as well as disease-related genes have been linked to altered drug sensitivity. However, identifying the correlation between this variability and pharmacological responses remains challenging due to the heterogeneity of cancer biology and the intricate interplay between cell lines and drug molecules. Here, we propose a network-based strategy that exploits information on gene expression and somatic mutations of CCLs to group cells according to their molecular similarity. We then identify genes that are characteristic of each cluster and correlate their status with drug response. We find that CCLs with similar characteristic active network regions present specific responses to certain drugs, and identify a limited set of genes that might be directly involved in drug sensitivity or resistance.

摘要

癌细胞系(CCLs)在药物发现的初始阶段起着重要作用,可用于筛选候选药物等。随着 CCL 面板的规模和多样性不断扩大,许多编码药物代谢酶、转运体和药物靶点的基因以及与疾病相关的基因中的多态性与药物敏感性的改变有关。然而,由于癌症生物学的异质性以及细胞系和药物分子之间的复杂相互作用,确定这种可变性与药理反应之间的相关性仍然具有挑战性。在这里,我们提出了一种基于网络的策略,该策略利用 CCL 的基因表达和体细胞突变信息将细胞根据其分子相似性进行分组。然后,我们确定每个聚类的特征基因,并将其状态与药物反应相关联。我们发现,具有相似特征活性网络区域的 CCL 对某些药物具有特定的反应,并确定了一组可能直接参与药物敏感性或耐药性的有限基因。

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