Helmholtz Center Munich, Institute of Computational Biology, 85764 Neuherberg, Germany.
Department of Biology, Ludwig-Maximilians University Munich, 82152 Martinsried, Germany.
Int J Mol Sci. 2021 Sep 20;22(18):10135. doi: 10.3390/ijms221810135.
Disparities between risk, treatment outcomes and survival rates in cancer patients across the world may be attributed to socioeconomic factors. In addition, the role of ancestry is frequently discussed. In preclinical studies, high-throughput drug screens in cancer cell lines have empowered the identification of clinically relevant molecular biomarkers of drug sensitivity; however, the genetic ancestry from tissue donors has been largely neglected in this setting. In order to address this, here, we show that the inferred ancestry of cancer cell lines is conserved and may impact drug response in patients as a predictive covariate in high-throughput drug screens. We found that there are differential drug responses between European and East Asian ancestries, especially when treated with PI3K/mTOR inhibitors. Our finding emphasizes a new angle in precision medicine, as cancer intervention strategies should consider the germline landscape, thereby reducing the failure rate of clinical trials.
世界各地癌症患者在风险、治疗效果和生存率方面的差异可能归因于社会经济因素。此外,人们经常讨论祖先的作用。在临床前研究中,癌症细胞系中的高通量药物筛选使人们能够识别出与临床相关的药物敏感性分子生物标志物;然而,在这种情况下,组织供体的遗传祖源在很大程度上被忽视了。为了解决这个问题,在这里,我们表明癌症细胞系的推断祖源是保守的,并可能作为高通量药物筛选中的预测协变量影响患者的药物反应。我们发现,欧洲和东亚血统之间存在不同的药物反应,特别是在用 PI3K/mTOR 抑制剂治疗时。我们的发现强调了精准医学的一个新角度,因为癌症干预策略应该考虑种系景观,从而降低临床试验的失败率。