Comparative genomic analysis of esophageal squamous cell carcinoma between Asian and Caucasian patient populations

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作者
Jiaying Deng
Hu Chen
Daizhan Zhou
Junhua Zhang
Yun Chen
Qi Liu
Dashan Ai
Hanting Zhu
Li Chu
Wenjia Ren
Xiaofei Zhang
Yi Xia
Menghong Sun
Huiwen Zhang
Jun Li
Xinxin Peng
Liang Li
Leng Han
Hui Lin
Xiujun Cai
Jiaqing Xiang
Shufeng Chen
Yihua Sun
Yawei Zhang
Jie Zhang
Haiquan Chen
Shijian Zhang
Yi Zhao
Yun Liu
Han Liang
Kuaile Zhao
机构
[1] Fudan University Shanghai Cancer Center,Department of Radiation Oncology
[2] Fudan University,Department of Oncology, Shanghai Medical College
[3] Baylor College of Medicine,Graduate Program in Quantitative and Computational Biosciences
[4] The University of Texas MD Anderson Cancer Center,Department of Bioinformatics and Computational Biology
[5] Zhejiang University School of Medicine,Department of General Surgery, Sir Run Run Shaw Hospital and Institute of Translational Medicine
[6] Zhejiang University,Innovation Center for Minimally Invasive Technique and Device
[7] Fudan University Shanghai Cancer Center,Department of Pathology
[8] The University of Texas Health Science Center at Houston McGovern Medical School,Department of Biochemistry and Molecular Biology
[9] The University of Texas MD Anderson Cancer Center,Department of Biostatistics
[10] Fudan University Shanghai Cancer Center,Department of Thoracic Surgery
[11] Precision Scientific (Beijing) Co.,Institute of Biomedical Sciences
[12] Ltd,Department of Systems Biology
[13] Fudan University,undefined
[14] The University of Texas MD Anderson Cancer Center,undefined
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摘要
Esophageal squamous cell carcinoma is a major histological type of esophageal cancer, with distinct incidence and survival patterns among races. Although previous studies have characterized somatic mutations in this disease, a rigorous comparison between different patient populations has not been conducted. Here we sequence the samples of 316 Chinese patients, combine them with those from The Cancer Genome Atlas, and perform a comparative analysis between Asian and Caucasian patients. We find that mutated CSMD3 is associated with better prognosis in Asian patients. Applying a robust computational strategy that adjusts for both technical and biological confounding factors, we find that TP53, EP300, and NFE2L2 show higher mutational frequencies in Asian patients. Moreover, NFE2L2 mutations correlate with the allele status of a nearby high-Fst SNP, suggesting their potential interaction. Our study provides insights into the molecular basis underlying the striking racial disparities of this disease, and represents a general computational framework for such a cross-population comparison.
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