Discovery and validation of prognostic markers in gastric cancer by genome-wide expression profiling

被引:39
|
作者
Zhang, Yue-Zheng [2 ,3 ]
Zhang, Lian-Hai [4 ]
Gao, Yang [2 ]
Li, Chao-Hua [2 ]
Jia, Shu-Qin [4 ]
Liu, Ni [4 ]
Cheng, Feng [2 ]
Niu, De-Yun [2 ,3 ]
Cho, William C. S. [5 ]
Ji, Jia-Fu [4 ]
Zeng, Chang-Qing [1 ,6 ]
机构
[1] Chinese Acad Sci, Beijing Inst Genom, Key Lab Genome Sci & Informat, Beijing 100029, Peoples R China
[2] Chinese Acad Sci, Beijing Inst Genom, CAS Key Lab Genome Sci & Informat, Beijing 100029, Peoples R China
[3] Chinese Acad Sci, Grad Sch, Beijing 100049, Peoples R China
[4] Peking Univ, Sch Oncol, Key Lab Carcinogenesis & Translat Res,Dept Surg, Minist Educ,Beijing Canc Hosp & Inst, Beijing 100142, Peoples R China
[5] Queen Elizabeth Hosp, Dept Clin Oncol, Hong Kong, Hong Kong, Peoples R China
[6] Chinese Acad Sci, Lab Canc Genom & Personalized Med, Beijing Inst Genom, Beijing 100029, Peoples R China
关键词
Gastric cancer; Gene expression profiling; Survival markers; Prognosis; Ribosomal proteins; RIBOSOMAL-PROTEIN L19; COLORECTAL-CANCER; BREAST-CANCER; SURVIVAL; PREDICTION; RESECTION; ADENOCARCINOMA; METASTASIS; RECURRENCE; CELLS;
D O I
10.3748/wjg.v17.i13.1710
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To develop a prognostic gene set that can predict patient overall survival status based on the whole genome expression analysis. METHODS: Using Illumina HumanWG-6 BeadChip followed by semi-supervised analysis, we analyzed the expression of 47 296 transcripts in two batches of gastric cancer patients who underwent surgical resection. Thirty-nine samples in the first batch were used as the training set to discover candidate markers correlated to overall survival, and thirty-three samples in the second batch were used for validation. RESULTS: A panel of ten genes were identified as prognostic marker in the first batch samples and classified patients into a low- and a high-risk group with significantly different survival times (P = 0.000047). This prognostic marker was then verified in an independent validation sample batch (P = 0.0009). By comparing with the traditional Tumor-node-metastasis (TNM) staging system, this ten-gene prognostic marker showed consistent prognosis results. It was the only independent prognostic value by multivariate Cox regression analysis (P = 0.007). Interestingly, six of these ten genes are ribosomal proteins, suggesting a possible association between the deregulation of ribosome related gene expression and the poor prognosis. CONCLUSION: A ten-gene marker correlated with overall prognosis, including 6 ribosomal proteins, was identified and verified, which may complement the predictive value of TNM staging system. (C) 2011 Baishideng. All rights reserved.
引用
收藏
页码:1710 / 1717
页数:8
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