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复制研究:系统鉴定癌细胞药物敏感性的基因组标记物。

Replication Study: Systematic identification of genomic markers of drug sensitivity in cancer cells.

机构信息

Indigo Biosciences, State College, United States.

Department of Veterinary and Biomedical Sciences, Pennsylvania State University, State College, United States.

出版信息

Elife. 2018 Jan 9;7:e29747. doi: 10.7554/eLife.29747.

Abstract

In 2016, as part of the Reproducibility Project: Cancer Biology, we published a Registered Report (Vanden Heuvel et al., 2016), that described how we intended to replicate selected experiments from the paper 'Systematic identification of genomic markers of drug sensitivity in cancer cells' (Garnett et al., 2012). Here we report the results. We found Ewing's sarcoma cell lines, overall, were more sensitive to the PARP inhibitor olaparib than osteosarcoma cell lines; however, while the effect was in the same direction as the original study (Figure 4C; Garnett et al., 2012), it was not statistically significant. Further, mouse mesenchymal cells transformed with either the or rearrangement displayed similar sensitivities to olaparib, whereas the Ewing's sarcoma cell line SK-N-MC had increased olaparib sensitivity. In the original study, mouse mesenchymal cells transformed with the rearrangement and SK-N-MC cells were found to have similar sensitivities to olaparib, whereas mesenchymal cells transformed with the rearrangement displayed a reduced sensitivity to olaparib (Figure 4E; Garnett et al., 2012). We also studied another Ewing's sarcoma cell line, A673: A673 cells depleted of or a negative control both displayed similar sensitivities to olaparib, whereas the original study reported a decreased sensitivity to olaparib when was depleted (Figure 4F; Garnett et al., 2012). Differences between the original study and this replication attempt, such as the use of different sarcoma cell lines and level of knockdown efficiency, are factors that might have influenced the outcomes. Finally, where possible, we report meta-analyses for each result.

摘要

2016 年,作为可重复性计划:癌症生物学的一部分,我们发表了一份注册报告(Vanden Heuvel 等人,2016 年),描述了我们打算如何复制论文“系统鉴定癌细胞中药物敏感性的基因组标记”(Garnett 等人,2012 年)中的选定实验。在这里,我们报告结果。我们发现尤文肉瘤细胞系总体上对 PARP 抑制剂奥拉帕利比骨肉瘤细胞系更敏感;然而,尽管效果与原始研究方向一致(图 4C;Garnett 等人,2012 年),但没有统计学意义。此外,用 或 重排转化的小鼠间充质细胞对奥拉帕利具有相似的敏感性,而尤文肉瘤细胞系 SK-N-MC 则对奥拉帕利的敏感性增加。在原始研究中,用 重排转化的小鼠间充质细胞和 SK-N-MC 细胞对奥拉帕利的敏感性相似,而用 重排转化的间充质细胞对奥拉帕利的敏感性降低(图 4E;Garnett 等人,2012 年)。我们还研究了另一种尤文肉瘤细胞系 A673:A673 细胞耗尽 或阴性对照均对奥拉帕利具有相似的敏感性,而原始研究报告说当耗尽 时,对奥拉帕利的敏感性降低(图 4F;Garnett 等人,2012 年)。原始研究和这次复制尝试之间的差异,例如使用不同的肉瘤细胞系和敲低效率水平,都是可能影响结果的因素。最后,在可能的情况下,我们报告了每个结果的荟萃分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8e3/5760202/c90d2297c987/elife-29747-fig1.jpg

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