Identification of predictors of drug sensitivity using patient-derived models of esophageal squamous cell carcinoma

被引:37
|
作者
Su, Dan [1 ,2 ,3 ]
Zhang, Dadong [4 ]
Jin, Jiaoyue [2 ,3 ]
Ying, Lisha [1 ,3 ,5 ]
Han, Miao [4 ]
Chen, Kaiyan [6 ]
Li, Bin [4 ]
Wu, Junzhou [1 ,3 ,5 ]
Xie, Zhenghua [4 ]
Zhang, Fanrong [7 ]
Lin, Yihui [4 ]
Cheng, Guoping [2 ]
Li, Jing-Yu [4 ]
Huang, Minran [1 ,3 ,5 ]
Wang, Jinchao [4 ]
Wang, Kailai [1 ]
Zhang, Jianjun [8 ,9 ]
Li, Fugen [4 ]
Xiong, Lei [4 ]
Futreal, Andrew [8 ,10 ]
Mao, Weimin [1 ,3 ,11 ]
机构
[1] Chinese Acad Sci, Inst Canc & Basic Med, Hangzhou, Zhejiang, Peoples R China
[2] Univ Chinese Acad Sci, Canc Hosp, Dept Pathol, Hangzhou, Zhejiang, Peoples R China
[3] Zhejiang Canc Hosp, Hangzhou, Zhejiang, Peoples R China
[4] 3D Med Inc, Res & Dev Inst Precis Med, Shanghai, Peoples R China
[5] Univ Chinese Acad Sci, Canc Hosp, Hangzhou, Zhejiang, Peoples R China
[6] Univ Chinese Acad Sci, Canc Hosp, Dept Chemotherapy, Hangzhou, Zhejiang, Peoples R China
[7] Univ Chinese Acad Sci, Canc Hosp, Dept Breast Surg, Hangzhou, Zhejiang, Peoples R China
[8] Univ Texas MD Anderson Canc Ctr, Dept Genom Med, Houston, TX 77030 USA
[9] Univ Texas MD Anderson Canc Ctr, Dept Thorac Head & Neck Med Oncol, Houston, TX 77030 USA
[10] Wellcome Trust Sanger Inst, Honorary Fac, Hinxton, England
[11] Univ Chinese Acad Sci, Canc Hosp, Dept Thorac Surg, Hangzhou, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
CANCER-CELLS; GENOMIC CHARACTERIZATION; XENOGRAFT MODELS; PD-1; BLOCKADE; COLON-CANCER; INHIBITION; TUMORS; AZATHIOPRINE; IMMUNOSUPPRESSION; ESTABLISHMENT;
D O I
10.1038/s41467-019-12846-7
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Previous studies from the Cancer Cell Line Encyclopedia (CCLE) project have adopted commercial pan-cancer cell line models to identify drug sensitivity biomarkers. However, drug sensitivity biomarkers in esophageal squamous cell carcinoma (ESCC) have not been widely explored. Here, eight patient-derived cell lines (PDCs) are successfully established from 123 patients with ESCC. The mutation profiling of PDCs can partially recapture the tumor tissue actionable mutations from 161 patients with ESCC. Based on these mutations and relative pathways in eight PDCs, 46 targeted drugs are selected for screening. Interestingly, some drug and biomarker relationships are established that were not discovered in the CCLE project. For example, CDKN2A or CDKN2B loss is significantly associated with the sensitivity of CDK4/6 inhibitors. Furthermore, both PDC xenografts and patient-derived xenografts confirm CDKN2A/2B loss as a biomarker predictive of CDK4/6 inhibitor sensitivity. Collectively, patient-derived models could predict targeted drug sensitivity associated with actionable mutations in ESCC.
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页数:13
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