URG11 Regulates Prostate Cancer Cell Proliferation, Migration, and Invasion.

Upregulated gene 11 (URG11), a new gene upregulated by hepatitis B virus X protein, is involved in the development and progression of several tumors, including liver, stomach, lung, and colon cancers. However, the role of URG11 in prostate cancer remains yet to be elucidated. By determined expressio...

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Publicado en:BioMed Research International Vol. 2018; pp. 1 - 11
Autores principales: Pan, Bin, Ye, Yunlin, Liu, Haiping, Zhen, Jianli, Zhou, Hongmei, Li, Yutong, Qu, Lijun, Wu, Youke, Zeng, Chuanrong, Zhong, Weifeng
Formato: pictorial research tables/charts Journal Article
Publicado: Wiley-Blackwell 5/31/2018
Acceso en línea:Ver este registro en EBSCOhost
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      dt: 5/31/2018
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      pub: Wiley-Blackwell
      place: Malden, Massachusetts
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        129884004
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        10.1155/2018/4060728
        129884004
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        atl: URG11 Regulates Prostate Cancer Cell Proliferation, Migration, and Invasion.
      aug:
        au:
          Pan, Bin
          Ye, Yunlin
          Liu, Haiping
          Zhen, Jianli
          Zhou, Hongmei
          Li, Yutong
          Qu, Lijun
          Wu, Youke
          Zeng, Chuanrong
          Zhong, Weifeng
        affil: Department of Urology, The First Affiliated Hospital, Jinan University, Guangzhou, China
      sug:
        subj:
          Prostatic Neoplasms Physiopathology
          Cell Line, Tumor
          Cell Migration Inhibition
          Genes
          Human
          Male
          Hepatitis B Physiopathology
          Prostatic Hypertrophy Diagnosis
          Apoptosis
          Prostatic Neoplasms Therapy
          Analysis of Variance
          Male
      ab: Upregulated gene 11 (URG11), a new gene upregulated by hepatitis B virus X protein, is involved in the development and progression of several tumors, including liver, stomach, lung, and colon cancers. However, the role of URG11 in prostate cancer remains yet to be elucidated. By determined expression in human prostate cancer tissues, URG11 was found significantly upregulated and positively correlated with the severity of prostate cancer, compared with that in benign prostatic hyperplasia tissues. Further, the mRNA and protein levels of URG11 were significantly upregulated in human prostate cancer cell lines (DU145, PC3, and LNCaP), compared with human prostate epithelial cell line (RWPE-1). Moreover, by the application of siRNA against URG11, the proliferation, migration, and invasion of prostate cancer cells were markedly inhibited. Genetic knockdown of URG11 also induced cell cycle arrest at G1/S phase, induced apoptosis, and decreased the expression level of β-catenin in prostate cancer cells. Overexpression of URG11 promoted the expression of β-catenin, the growth, the migration, and invasion ability of prostate cancer cells. Taken together, this study reveals that URG11 is critical for the proliferation, migration, and invasion in prostate cancer cells, providing the evidence of URG11 to be a novel potential therapeutic target of prostate cancer.
      pubtype: Academic Journal
      doctype:
        pictorial
        research
        tables/charts
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      ougenre: Article
    language: English
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