Oxidized low-density lipoprotein is associated with advanced-stage prostate cancer
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  • 作者:Fangning Wan ; Xiaojian Qin ; Guiming Zhang ; Xiaolin Lu ; Yao Zhu…
  • 关键词:Ox ; LDL ; OLR1 ; Cell migration ; Prostate cancer ; Proliferation
  • 刊名:Tumor Biology
  • 出版年:2015
  • 出版时间:May 2015
  • 年:2015
  • 卷:36
  • 期:5
  • 页码:3573-3582
  • 全文大小:3,229 KB
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  • 作者单位:Fangning Wan (1) (2)
    Xiaojian Qin (1) (2)
    Guiming Zhang (1) (2)
    Xiaolin Lu (1) (2)
    Yao Zhu (1) (2)
    Hailiang Zhang (1) (2)
    Bo Dai (1) (2)
    Guohai Shi (1) (2)
    Dingwei Ye (1) (2)

    1. Department of Urology, Fudan University Shanghai Cancer Center, Shanghai, People’s Republic of China
    2. Department of Oncology, Shanghai Medical College, Fudan University, No. 270, Dong’an Road, Shanghai, 200032, People’s Republic of China
  • 刊物主题:Cancer Research;
  • 出版者:Springer Netherlands
  • ISSN:1423-0380
文摘
Clinical and epidemiological data suggest coronary artery disease shares etiology with prostate cancer (PCa). The aim of this work was to assess the effects of several serum markers reported in cardiovascular disease on PCa. Serum markers (oxidized low-density lipoprotein [ox-LDL], apolipoprotein [apo] B100, and apoB48) in peripheral blood samples from 50 patients from Fudan University Shanghai Cancer Center (FUSCC) with localized or lymph node metastatic PCa were investigated in this study. Twenty-five samples from normal individuals were set as controls. We first conducted enzyme-linked immunosorbent assay analysis to select candidate markers that were significantly different between these patients and controls. Then, the clinical relevance between OLR1 (the ox-LDL receptor) expression and PCa was analyzed in The Cancer Genome Atlas (TCGA) cohort. We also investigated the function of ox-LDL in PCa cell lines in vitro. Phosphorylation protein chips were used to analyze cell signaling pathways in ox-LDL-treated PC-3 cells. The ox-LDL level was found to be significantly correlated with N stage of prostate cancer. OLR1 expression was correlated with lymph node metastasis in the TCGA cohort. In vitro, ox-LDL stimulated the proliferation, migration, and invasion of LNCaP and PC-3 in a dose-dependent manner. The results of phosphoprotein microarray illustrated that ox-LDL could influence multiple signaling pathways of PC-3. Activation of proliferation promoting signaling pathways (including β-catenin, cMyc, NF-κB, STAT1, STAT3) as well as apoptosis-associating signaling pathways (including p27, caspase-3) demonstrated that ox-LDL had complicated effects on prostate cancer. Increased serum ox-LDL level and OLR1 expression may indicate advanced-stage PCa and lymph node metastasis. Moreover, ox-LDL could stimulate PCa proliferation, migration, and invasion in vitro.

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