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基因表达谱分析揭示了亚洲人群食管鳞癌的不同分子亚型。

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

机构信息

Department of Preventive Medicine, Institute of Biomedical Informatics, Joint National Laboratory for Antibody Drug Engineering, Cell Signal Transduction Laboratory, School of Basic Medical Sciences, Henan University, Kaifeng 475004, China.

Henan Key Laboratory of Cancer Epigenetics, Cancer Hospital, The First Affiliated Hospital, College of Clinical Medicine, Medical College of Henan University of Science and Technology, Luoyang 471003, China.

出版信息

Neoplasia. 2019 Jun;21(6):571-581. doi: 10.1016/j.neo.2019.03.013. Epub 2019 Apr 29.

Abstract

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.

摘要

食管鳞状细胞癌(ESCC)是世界上最常见的癌症之一,尤其在亚洲人群中较为普遍,且对常规治疗反应不佳。通过分子分析对 ESCC 进行细分是一种强有力的策略,可以扩展常规的临床病理分类,改善预后和治疗效果。在这里,我们使用基因表达谱数据在中国人群中鉴定出两种 ESCC 分子亚型,并在另外两个独立的亚洲人群(日本人和越南人)中进一步验证了这两种分子亚型。I 型 ESCC 富集了包括免疫反应在内的途径,而 II 型 ESCC 中过表达的基因主要涉及外胚层发育、糖酵解过程和细胞增殖。具体来说,我们鉴定出了一些潜在的 ESCC 亚型特异性诊断标志物(I 型为 FOXA1 和 EYA2,II 型为 LAMC2 和 KRT14),并在第四个亚洲队列中进行了验证。此外,我们还为 ESCC 提出了一些亚型特异性的治疗靶点,在进一步验证后,这些靶点可能为未来的 ESCC 临床治疗提供指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93f5/6495472/9d9b3ffedba0/gr1.jpg

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