Gene Expression Profiling Reveals Distinct Molecular Subtypes of Esophageal Squamous Cell Carcinoma in Asian Populations

被引:21
|
作者
Wang, Fengling [1 ]
Yan, Zhongyi [1 ]
Lv, Jiajia [1 ]
Xin, Junfang [1 ]
Dang, Yifang [1 ]
Sun, Xiaoxiao [1 ]
An, Yang [1 ]
Qi, Yijun [2 ]
Jiang, Qiying [1 ]
Zhu, Wan [3 ]
Li, Yongqiang [1 ]
Li, Ao [4 ]
Guo, Xiangqian [1 ]
机构
[1] Henan Univ, Sch Basic Med Sci, Cell Signal Transduct Lab,Dept Prevent Med, Joint Natl Lab Antibody Drug Engn,Inst Biomed Inf, Kaifeng 475004, Peoples R China
[2] Henan Univ Sci & Technol, Med Coll, Coll Clin Med, Affiliated Hosp 1,Canc Hosp,Henan Key Lab Canc Ep, Luoyang 471003, Peoples R China
[3] Stanford Univ, Dept Anesthesia, 300 Pasteur Dr, Stanford, CA 94305 USA
[4] Univ Sci & Technol China, Ctr Biomed Engn, Sch Informat Sci & Technol, Hefei, Anhui, Peoples R China
来源
NEOPLASIA | 2019年 / 21卷 / 06期
基金
中国国家自然科学基金;
关键词
GENOME-WIDE ASSOCIATION; POOR-PROGNOSIS; SUSCEPTIBILITY LOCI; CLINICAL-RESPONSE; LUNG-CANCER; RISK; TIGIT; IDENTIFICATION; EPIDEMIOLOGY; METABOLISM;
D O I
10.1016/j.neo.2019.03.013
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Esophageal squamous cell carcinoma (ESCC) is one of the most common cancers worldwide, particularly in Asian populations, and responds poorly to conventional therapy. Subclassification of ESCCs by molecular analysis is a powerful strategy in extending conventional clinicopathologic classification, improving prognosis and therapy. Here we identified two ESCC molecular subtypes in Chinese population using gene expression profiling data and further validated the molecular subtypes in two other independent Asian populations (Japanese and Vietnamese). Subtype I ESCCs were enriched in pathways including immune response, while genes overexpressed in subtype II ESCCs were mainly involved in ectoderm development, glycolysis process, and cell proliferation. Specifically, we identified potential ESCC subtype-specific diagnostic markers (FOXA1 and EYA2 for subtype I, LAMC2 and KRT14 for subtype II) and further validated them in a fourth Asian cohort. In addition, we propose a few subtype-specific therapeutic targets for ESCC, which may guide future ESCC clinical treatment when further validated.
引用
收藏
页码:571 / 581
页数:11
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