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      Identification of a novel glycolysis-related gene signature that can predict the survival of patients with lung adenocarcinoma

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          ABSTRACT

          Lung cancer is one of the most malignant cancers worldwide, and lung adenocarcinoma (LUAD) is the most common histologic subtype. Thousands of biomarkers related to the survival and prognosis of patients with this cancer type have been investigated through database mining; however, the prediction effect of a single gene biomarker is not satisfactorily specific or sensitive. Thus, the present study aimed to develop a novel gene signature of prognostic values for patients with LUAD. Using a data-mining method, we performed expression profiling of 1145 mRNAs in large cohorts with LUAD (n = 511) from The Cancer Genome Atlas database. Using the Gene Set Enrichment Analysis, we selected 198 genes related to GLYCOLYSIS, which is the most important enrichment gene set. Moreover, these genes were identified using Cox proportional regression modeling. We established a risk score staging system to predict the outcome of patients with LUAD and subsequently identified four genes ( AGRN, AKR1A1, DDIT4, and HMMR) that were closely related to the prognosis of patients with LUAD. The identified genes allowed us to classify patients into the high-risk group (with poor outcome) and low-risk group (with better outcome). Compared with other clinical factors, the risk score has a better performance in predicting the outcome of patients with LUAD, particularly in the early stage of LUAD. In conclusion, we developed a four-gene signature related to glycolysis by utilizing the Cox regression model and a risk staging model for LUAD, which might prove valuable for the clinical management of patients with LUAD.

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          Author and article information

          Journal
          Cell Cycle
          Cell Cycle
          KCCY
          kccy20
          Cell Cycle
          Taylor & Francis
          1538-4101
          1551-4005
          2019
          17 February 2019
          : 18
          : 5
          : 568-579
          Affiliations
          [a ] Department of Radiation Oncology, The First Affiliated Hospital of China Medical University , Shenyang, China
          [b ] Department of Ultrasound, The First Affiliated Hospital of China Medical University , Shenyang, China
          [c ] Department of Pharmacology, School of Pharmacy, China Medical University , Shenyang, China
          Author notes
          Article
          PMC6464579 PMC6464579 6464579 1578146
          10.1080/15384101.2019.1578146
          6464579
          30727821
          e678a861-a550-478e-b2fa-70236cfb570e
          © 2019 Informa UK Limited, trading as Taylor & Francis Group
          History
          : 16 September 2018
          : 22 November 2018
          : 12 December 2018
          Page count
          Figures: 6, Tables: 4, References: 22, Pages: 12
          Funding
          Funded by: National Natural Science Foundation of China 10.13039/501100001809
          Award ID: No. U1608281
          Funded by: Natural Science Foundation of Liaoning Province 10.13039/501100005047
          Award ID: No.2013225021
          Funded by: Program for New Century Excellent Talents in University 10.13039/501100004602
          Award ID: No. LJQ2015118
          This study was supported by theNational Natural Science Foundation of China [No. U1608281]; Natural Science Foundation of Liaoning Province [No.2013225021]; Program for New Century Excellent Talents in University [No. LJQ2015118].
          Categories
          Research Paper

          glycolysis,survival,prognostic,mRNAs,Lung cancer
          glycolysis, survival, prognostic, mRNAs, Lung cancer

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