Literature DB >> 32048287

A 16-mRNA signature optimizes recurrence-free survival prediction of Stages II and III gastric cancer.

Ke Peng1, Erbao Chen1, Wei Li1, Xi Cheng1, Yiyi Yu1, Yuehong Cui1, Qian Li1, Yan Wang1, Xiaojing Xu1, Cheng Tang1, Lu Gan1, Shan Yu1, Tianshu Liu1.   

Abstract

High-throughput messenger RNA (mRNA) analysis has become a powerful tool for exploring tumor recurrence or metastasis mechanisms. Here, we constructed a signature to predict the recurrence risk of Stages II and III gastric cancer (GC) patients. A least absolute shrinkage and selection operator method Cox regression model was utilized to construct the signature. Using this method, a 16-mRNA signature was identified to be associated with the relapse-free survival of Stages II and III GCs in training dataset GSE62254 (n = 194). Then this signature was validated in an independent Gene Expression Omnibus cohort GSE26253 (n = 297) and a dataset of The Cancer Genome Atlas (TCGA; n = 235). This classifier could successfully screen out the high-risk Stages II and III GCs in the training cohort (hazard ratio [HR] = 40.91; 95% confidence interval [CI] = 5.58-299.7; p < .0001). Analysis in two independent validation cohorts yielded consistent results (GSE26253: HR = 1.69, 95% CI = 1.17-2.43,; p = .0045; TCGA: HR = 2.01, 95% CI = 1.13-3.56, p = .0146). Cox regression analyses revealed that the risk score derived from this signature was an independent risk factor in Stages II and III GCs. Besides, a nomogram was constructed to serve clinical practice. Through gene set variation analysis, we found several gene sets associated with chemotherapeutic drug resistance and tumor metastasis significantly enriched in high-risk patients. In summary, this 16-mRNA signature can be used as a powerful tool for prognostic evaluation and help clinicians identify high-risk patients.
© 2020 Wiley Periodicals, Inc.

Entities:  

Keywords:  LASSO; gastric cancer; relapse-free survival; signature

Mesh:

Substances:

Year:  2020        PMID: 32048287     DOI: 10.1002/jcp.29511

Source DB:  PubMed          Journal:  J Cell Physiol        ISSN: 0021-9541            Impact factor:   6.384


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