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基于癌症基因组图谱肿瘤转录组概况发现克服卵巢癌化疗耐药性的药物。

Discovering drugs to overcome chemoresistance in ovarian cancers based on the cancer genome atlas tumor transcriptome profile.

作者信息

Wang Fan, Chang Jeremy T-H, Zhang Zhenyu, Morrison Gladys, Nath Aritro, Bhutra Steven, Huang Rong Stephanie

机构信息

Section of Hematology/Oncology, Department of Medicine, University of Chicago, Chicago, IL, USA.

Biological Sciences Collegiate Division, University of Chicago, Chicago, IL, USA.

出版信息

Oncotarget. 2017 Dec 4;8(70):115102-115113. doi: 10.18632/oncotarget.22870. eCollection 2017 Dec 29.

Abstract

Ovarian cancer accounts for the highest mortality among gynecologic cancers, mainly due to intrinsic or acquired chemoresistance. While mechanistic-based methods have been used to identify compounds that can overcome chemoresistance, an effective comprehensive drug screening has yet to be developed. We applied a transcriptome based drug sensitivity prediction method, to the Cancer Genome Atlas (TCGA) ovarian cancer dataset to impute patient tumor response to over 100 different drugs. By stratifying patients based on their predicted response to standard of care (SOC) chemotherapy, we identified drugs that are likely more sensitive in SOC resistant ovarian tumors. Five drugs (ABT-888, BIBW2992, gefitinib, AZD6244 and lenalidomide) exhibit higher efficacy in SOC resistant ovarian tumors when multi-platform of transcriptome profiling methods were employed. Additional and clinical sample validations were carried out and verified the effectiveness of these agents. Our candidate drugs hold great potential to improve clinical outcome of chemoresistant ovarian cancer.

摘要

卵巢癌在妇科癌症中死亡率最高,主要原因是内在或获得性化疗耐药性。虽然基于机制的方法已被用于识别能够克服化疗耐药性的化合物,但尚未开发出有效的综合药物筛选方法。我们将基于转录组的药物敏感性预测方法应用于癌症基因组图谱(TCGA)卵巢癌数据集,以估算患者肿瘤对100多种不同药物的反应。通过根据患者对标准治疗(SOC)化疗的预测反应进行分层,我们确定了在SOC耐药性卵巢肿瘤中可能更敏感的药物。当采用多平台转录组分析方法时,五种药物(ABT-888、BIBW2992、吉非替尼、AZD6244和来那度胺)在SOC耐药性卵巢肿瘤中表现出更高的疗效。进行了额外的临床样本验证并证实了这些药物的有效性。我们的候选药物在改善化疗耐药性卵巢癌的临床结果方面具有巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddcc/5777757/6518eca8677c/oncotarget-08-115102-g001.jpg

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