Journal of Biochemical and Molecular Toxicology · 2018 · 52 citations · 32 references
Life SciencesCancer BiologyOncologyApoptosisGene ExpressionMolecular OncologyApoptosis In CancerApoptosis RegulationApoptotic SignalingCancer Cell SignalingProstate CancerTumor Suppressor GenesApoptosis DysregulationApoptotic Signaling In CancerCancer Cell Proliferation InhibitionCaspase CleavageCell Proliferation IndicesP21 RegulationProstate CarcinogenesisProstate Specimens
Here, we aimed to investigate the carcinogenic effects of apolipoprotein C1 (APOC1) in prostate cancer (PCa). APOC1 expression was evaluated in PCa and normal prostate specimens, and lentivirus-mediated RNA interference was used to knockdown APOC1 in DU145 cells. The effects of APOC1 silencing on cell proliferation, cell cycle arrest, and apoptosis were assessed. APOC1 expression was much higher in PCa tissues than in normal tissues. Moreover, APOC1 silencing inhibited cell proliferation and colony formation, arrested cell cycle progression, and enhanced apoptosis in DU145 cells. Additionally, APOC1 silencing decreased survivin, phospho-Rb, and p21 levels and increased cleaved caspase-3 expression. These data supported the procarcinogenic effects of APOC1 in the pathogenesis of PCa and suggested that targeting APOC1 may have applications in the treatment of PCa.
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Cancer statistics in China, 2015
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