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Research Article

Identification of three lncRNA-related prognostic signatures in gastric cancer by integrated multi-omics analysis

    Haoqin Jiang‡

    Department of Laboratory Medicine, Huashan Hospital Fudan University, Shanghai, 200040, China

    ,
    Jun Wang‡

    Department of General Surgery, Huashan Hospital, Fudan University, Shanghai, 200040, China

    ,
    Yingxiao Song‡

    Department of Gastroenterology, Changhai Hospital, The Naval Medical University, Shanghai, 222300, China

    ,
    Jian Chen

    Department of Laboratory Medicine, Huashan Hospital Fudan University, Shanghai, 200040, China

    ,
    Liu Dong

    Department of Laboratory Medicine, Huashan Hospital Fudan University, Shanghai, 200040, China

    ,
    Qianqian Xu

    Department of Laboratory Medicine, Huashan Hospital Fudan University, Shanghai, 200040, China

    ,
    Ruoshui Cao

    Department of Laboratory Medicine, Huashan Hospital Fudan University, Shanghai, 200040, China

    ,
    Yuting Wang

    Department of Laboratory Medicine, Huashan Hospital Fudan University, Shanghai, 200040, China

    ,
    Xiao Xu

    Department of Laboratory Medicine, Huashan Hospital Fudan University, Shanghai, 200040, China

    ,
    Xinju Zhang

    Department of Laboratory Medicine, Huashan Hospital Fudan University, Shanghai, 200040, China

    ,
    Fanyang Kong§

    Department of Gastroenterology, Changhai Hospital, The Naval Medical University, Shanghai, 222300, China

    ,
    Ming Guan§

    Department of Laboratory Medicine, Huashan Hospital Fudan University, Shanghai, 200040, China

    &
    Xuan Deng§

    *Author for correspondence:

    E-mail Address: mignonxuan@163.com

    Department of Laboratory Medicine, Huashan Hospital Fudan University, Shanghai, 200040, China

    Published Online:https://doi.org/10.2217/epi-2023-0349

    Aims: The systematic identification of molecular features correlated with the clinical status of gastric cancer (GC) in patients is significant, although such investigation remains insufficient. Methods: GC subtyping based on RNA sequencing, copy number variation and DNA methylation data were derived from The Cancer Genome Atlas program. Prognostics lncRNA biomarkers for GC were identified by univariate Cox, LASSO and SVM-RFE analysis. Results: Three molecular subtypes with significant survival discrepancies, and their specific DEmRNAs and DElncRNAs were identified. Three reliable prognostic-associated lncRNA, including LINC00670, LINC00452 and LINC00160, were selected for GC. Conclusion: Our findings expanded the understanding on the regulatory network of lncRNAs in GC, providing potential targets for prognosis and treatment of GC patients.

    Papers of special note have been highlighted as: • of interest; •• of considerable interest

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