Silencing CAPN2 Expression Inhibited Castration-Resistant Prostate Cancer Cells Proliferation and Invasion via AKT/mTOR Signal Pathway.

The mRNA expression of CAPN2 was upregulated in CRPC cells (DU145 and PC3) than that in non-CRPC cells. Silencing CAPN2 expression could inhibit DU145 and PC3 cells proliferation by cell cycle arrest at G1 phase. Knockdown of CPAN2 level suppressed the migration and invasion capacity of CRPC cells b...

Descripción completa

Detalles Bibliográficos
Publicado en:BioMed Research International Vol. 2017; pp. 1 - 11
Autores principales: Li, Pu, Miao, Chenkui, Liang, Chao, Shao, Pengfei, Wang, Zengjun, Li, Jie
Formato: pictorial research tables/charts Journal Article
Publicado: Wiley-Blackwell 2/9/2017
Acceso en línea:Ver este registro en EBSCOhost
fields @attributes:
  recordID: 1
pdfLink:
plink: https://search.ebscohost.com/login.aspx?direct=true&db=ccm&AN=121197463&site=ehost-live
header:
  @attributes:
    shortDbName: ccm
    uiTerm: 121197463
    longDbName: CINAHL Complete
    uiTag: AN
  controlInfo:
    bkinfo:
    dissinfo:
    jinfo:
      jid:
        23146133
        FT2T
      jtl: BioMed Research International
      issn: 23146133
      maglogo: N
    pubinfo:
      dt: 2/9/2017
      vid: 2017
      pid: 480
      pub: Wiley-Blackwell
      place: Malden, Massachusetts
    artinfo:
      ui:
        121197463
        121197463
        121197463
        10.1155/2017/2593674
        121197463
      ppf: 1
      ppct: 10
      formats:
        fmt:
          @attributes:
            type: P
      tig:
        atl: Silencing CAPN2 Expression Inhibited Castration-Resistant Prostate Cancer Cells Proliferation and Invasion via AKT/mTOR Signal Pathway.
      aug:
        au:
          Li, Pu
          Miao, Chenkui
          Liang, Chao
          Shao, Pengfei
          Wang, Zengjun
          Li, Jie
        affil: State Key Laboratory of Reproductive Medicine and Department of Urology, The First Affiliated Hospital, Nanjing Medical University, Nanjing 210029, China
      sug:
        subj:
          Prostatic Neoplasms, Castration-Resistant
          Neoplasm Invasiveness
          Cell Cycle
          RNA Physiology
          Gene Expression
          Intracellular Signaling Peptides and Proteins
          Signal Transduction
          Human
          Male
          Middle Age
          Aged
          Descriptive Statistics
          Data Analysis Software
          P-Value
          T-Tests
          Cell Culture Techniques
          Blotting, Western
          Polymerase Chain Reaction
          Cytological Techniques
          Immunohistochemistry
          Funding Source
          Middle Aged: 45-64 years
          Aged: 65+ years
          Male
      ab: The mRNA expression of CAPN2 was upregulated in CRPC cells (DU145 and PC3) than that in non-CRPC cells. Silencing CAPN2 expression could inhibit DU145 and PC3 cells proliferation by cell cycle arrest at G1 phase. Knockdown of CPAN2 level suppressed the migration and invasion capacity of CRPC cells by reducing matrix metalloproteinase-2 (MMP-2) and MMP-9 activation, as well as repressing the phosphorylation protein expression of AKT and mTOR. In addition, we found that the expression of CAPN2 was elevated in Pca tissues than that in normal control tissues. Therefore, we showed the important roles of CAPN2 in the development and progression in CRPC cells, suggesting a new therapeutic intervention for treating castration-resistant prostate cancer patients.
      pubtype: Academic Journal
      doctype:
        pictorial
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
    refInfo:
    holdings:
      @attributes:
        islocal: N