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LncRNA DPP10-AS1 promotes malignant processes through epigenetically activating its cognate gene DPP10 and predicts poor prognosis in lung cancer patients

机译:LncRNA DPP10-AS1 promotes malignant processes through epigenetically activating its cognate gene DPP10 and predicts poor prognosis in lung cancer patients

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摘要

Objective:The purpose of this study was to explore the function and gene expression regulation of the newly identified lnc RNA DPP10-AS1 in lung cancer,and its potential value as a prognostic biomarker.Methods:q RT-PCR and Western blot were conducted to detect the expression of DDP10-AS1 and DPP10 in lung cancer cell lines and tissues.The effects of DDP10-AS1 on DPP10 expression,cell growth,invasion,apoptosis,and in vivo tumor growth were investigated in lung cancer cells by Western blot,rescue experiments,colony formation,flow cytometry,and xenograft animal experiments.Results:The novel antisense lnc RNA DPP10-AS1 was found to be highly expressed in cancer tissues(P<0.0001),and its upregulation predicted poor prognosis in patients with lung cancer(P=0.0025).Notably,DPP10-AS1 promoted lung cancer cell growth,colony formation,and cell cycle progression,and repressed apoptosis in lung cancer cells by upregulating DPP10 expression.Additionally,DPP10-AS1 facilitated lung tumor growth via upregulation of DPP10 protein in a xenograft mouse model.Importantly,DPP10-AS1 positively regulated DPP10 gene expression,and both were coordinately upregulated in lung cancer tissues.Mechanically,DPP10-AS1 was found to associate with DPP10 m RNA but did not enhance DPP10 m RNA stability.Hypomethylation of DPP10-AS1 and DPP10 contributed to their coordinate upregulation in lung cancer.Conclusions:These findings indicated that the upregulation of the antisense lnc RNA DPP10-AS1 promotes lung cancer malignant processes and facilitates tumorigenesis by epigenetically regulating its cognate sense gene DPP10.DPP10-AS1 may serve as a candidate prognostic biomarker and a potential therapeutic target in lung cancer.

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  • 来源
    《癌症生物学与医学(英文版 )》 |2021年第3期|675-692|共18页
  • 作者单位

    Department of Biochemistry and Molecular Biology Ningbo University School of Medicine Ningbo 315211 China;

    Zhejiang Province Key Laboratory of Pathophysiology Ningbo University School of Medicine Ningbo 315211 China;

    Department of Biochemistry and Molecular Biology Ningbo University School of Medicine Ningbo 315211 China;

    Zhejiang Province Key Laboratory of Pathophysiology Ningbo University School of Medicine Ningbo 315211 China;

    Department of Biochemistry and Molecular Biology Ningbo University School of Medicine Ningbo 315211 China;

    Zhejiang Province Key Laboratory of Pathophysiology Ningbo University School of Medicine Ningbo 315211 China;

    Department of Biochemistry and Molecular Biology Ningbo University School of Medicine Ningbo 315211 China;

    Zhejiang Province Key Laboratory of Pathophysiology Ningbo University School of Medicine Ningbo 315211 China;

    Department of Biochemistry and Molecular Biology Ningbo University School of Medicine Ningbo 315211 China;

    Department of Thoracic Surgery The Affiliated Hospital of Ningbo University School of Medicine Ningbo 315020 China;

    Department of Thoracic Surgery The Affiliated Lihuili Hospital of Ningbo University Ningbo 315048 China;

    Department of Thoracic Surgery The Affiliated Lihuili Hospital of Ningbo University Ningbo 315048 China;

    Department of Thoracic Surgery The Affiliated Lihuili Hospital of Ningbo University Ningbo 315048 China;

    Department of Biochemistry and Molecular Biology Ningbo University School of Medicine Ningbo 315211 China;

    Zhejiang Province Key Laboratory of Pathophysiology Ningbo University School of Medicine Ningbo 315211 China;

    Department of Biochemistry and Molecular Biology Ningbo University School of Medicine Ningbo 315211 China;

    Zhejiang Province Key Laboratory of Pathophysiology Ningbo University School of Medicine Ningbo 315211 China;

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