Sonkin Dmitriy
Division of Cancer Treatment and Diagnosis, National Cancer Institute, Rockville, United States.
Elife. 2015 Oct 22;4:e10279. doi: 10.7554/eLife.10279.
A number of TP53-MDM2 inhibitors are currently under investigation as therapeutic agents in a variety of clinical trials in patients with TP53 wild type tumors. Not all wild type TP53 tumors are sensitive to such inhibitors. In an attempt to improve selection of patients with TP53 wild type tumors, an mRNA expression signature based on 13 TP53 transcriptional target genes was recently developed (Jeay et al. 2015). Careful reanalysis of TP53 status in the study validation data set of cancer cell lines considered to be TP53 wild type detected TP53 inactivating alterations in 23% of cell lines. The subsequent reanalysis of the remaining TP53 wild type cell lines clearly demonstrated that unfortunately the 13-gene signature cannot predict response to TP53-MDM2 inhibitor in TP53 wild type tumors.
目前,多种TP53-MDM2抑制剂正在各类针对TP53野生型肿瘤患者的临床试验中作为治疗药物进行研究。并非所有野生型TP53肿瘤都对这类抑制剂敏感。为了改进TP53野生型肿瘤患者的筛选,最近基于13个TP53转录靶基因开发了一种mRNA表达特征(Jeay等人,2015年)。在被认为是TP53野生型的癌细胞系研究验证数据集中,对TP53状态进行仔细重新分析后,在23%的细胞系中检测到TP53失活改变。随后对其余TP53野生型细胞系的重新分析清楚地表明,遗憾的是,13基因特征无法预测TP53野生型肿瘤对TP53-MDM2抑制剂的反应。