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Validity of patient-derived xenograft mouse models for lung cancer based on exome sequencing data

机译:基于Exome测序数据的肺癌患者衍生的异种移植小鼠模型的有效性

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Patient-derived xenograft (PDX) mouse models are frequently used to test the drug efficacy in diverse types of cancer. They are known to recapitulate the patient characteristics faithfully, but a systematic survey with a large number of cases is yet missing in lung cancer. Here we report the comparison of genomic characters between mouse and patient tumor tissues in lung cancer based on exome sequencing data. We established PDX mouse models for 132 lung cancer patients and performed whole exome sequencing for trio samples of tumor-normal-xenograft tissues. Then we computed the somatic mutations and copy number variations, which were used to compare the PDX and patient tumor tissues. Genomic and histological conclusions for validity of PDX models agreed in most cases, but we observed eight (~7%) discordant cases. We further examined the changes in mutations and copy number alterations in PDX model production and passage processes, which highlighted the clonal evolution in PDX mouse models. Our study shows that the genomic characterization plays complementary roles to the histological examination in cancer studies utilizing PDX mouse models.
机译:患者衍生的异种移植物(PDX)小鼠模型经常用于在不同类型的癌症中测试药物功效。众所周知,他们忠实地重新承载患者特征,但肺癌缺少具有大量病例的系统调查。在这里,我们在基于外壳测序数据的基础上报告了小鼠和患者肿瘤组织之间基因组特征的比较。我们为132名肺癌患者建立了PDX小鼠模型,并对肿瘤 - 正常卵转移组织的三重血样品进行了全面的exome测序。然后,我们计算了体细胞突变和拷贝数变异,其用于比较PDX和患者肿瘤组织。在大多数情况下,PDX模型有效性的基因组和组织学结论,但我们观察到八(〜7%)不和谐的病例。我们进一步检查了PDX模型生产和通道过程中突变和拷贝数改变的变化,这突出显示了PDX鼠标模型中的克隆演化。我们的研究表明,基因组特征在利用PDX小鼠模型的癌症研究中的组织学检查起着互补的作用。

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