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Identification of a novel cell cycle-related gene signature predicting survival in patients with gastric cancer.
Zhao, Lan; Jiang, Longyang; He, Linxiu; Wei, Qian; Bi, Jia; Wang, Yan; Yu, Lifeng; He, Miao; Zhao, Lin; Wei, Minjie.
Afiliação
  • Zhao L; Department of Pharmacology, School of Pharmacy, China Medical University, Shenyang, Liaoning, China.
  • Jiang L; Liaoning Key Laboratory of Molecular Targeted Anti-tumor Drug Development and Evaluation, Department of Pharmacology, School of Pharmacy, China Medical University, Shenyang, Liaoning, China.
  • He L; Department of Pharmacology, School of Pharmacy, China Medical University, Shenyang, Liaoning, China.
  • Wei Q; Liaoning Key Laboratory of Molecular Targeted Anti-tumor Drug Development and Evaluation, Department of Pharmacology, School of Pharmacy, China Medical University, Shenyang, Liaoning, China.
  • Bi J; Department of Pharmacology, School of Pharmacy, China Medical University, Shenyang, Liaoning, China.
  • Wang Y; Liaoning Key Laboratory of Molecular Targeted Anti-tumor Drug Development and Evaluation, Department of Pharmacology, School of Pharmacy, China Medical University, Shenyang, Liaoning, China.
  • Yu L; Department of Pharmacology, School of Pharmacy, China Medical University, Shenyang, Liaoning, China.
  • He M; Liaoning Key Laboratory of Molecular Targeted Anti-tumor Drug Development and Evaluation, Department of Pharmacology, School of Pharmacy, China Medical University, Shenyang, Liaoning, China.
  • Zhao L; Department of Pharmacology, School of Pharmacy, China Medical University, Shenyang, Liaoning, China.
  • Wei M; Liaoning Key Laboratory of Molecular Targeted Anti-tumor Drug Development and Evaluation, Department of Pharmacology, School of Pharmacy, China Medical University, Shenyang, Liaoning, China.
J Cell Physiol ; 234(5): 6350-6360, 2019 05.
Article em En | MEDLINE | ID: mdl-30238991
ABSTRACT
Gastric cancer (GC) is one of the most fatal cancers in the world. Thousands of biomarkers have been explored that might be related to survival and prognosis via database mining. However, the prediction effect of single gene biomarkers is not specific enough. Increasing evidence suggests that gene signatures are emerging as a possible better alternative. We aimed to develop a novel gene signature to improve the prognosis prediction of GC. Using the messenger RNA (mRNA)-mining approach, we performed mRNA expression profiling in a large GC cohort (n = 375) from The Cancer Genome Atlas (TCGA) database. Gene Set Enrichment Analysis (GSEA) was performed, and we recovered genes related to the G2/M checkpoint, which we identified with a Cox proportional regression model. We identified a set of five genes (MARCKS, CCNF, MAPK14, INCENP, and CHAF1A), which were significantly associated with overall survival (OS) in the test series. Based on this five-gene signature, the test series patients could be classified into high-risk or low-risk subgroups. Multivariate Cox regression analysis indicated that the prognostic power of this five-gene signature was independent of clinical features. In conclusion, we developed a five-gene signature related to the cell cycle that can predict survival for GC. Our findings provide novel insight that is useful for understanding cell cycle mechanisms and for identifying patients with GC with poor prognoses.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Gástricas / Adenocarcinoma / Biomarcadores Tumorais / Ciclo Celular / Transcriptoma Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Cell Physiol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Gástricas / Adenocarcinoma / Biomarcadores Tumorais / Ciclo Celular / Transcriptoma Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Cell Physiol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China