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10.3892/or.2017.5719

http://scihub22266oqcxt.onion/10.3892/or.2017.5719
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C5562001!5562001 !28627623
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suck abstract from ncbi


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pmid28627623
      Oncol+Rep 2017 ; 38 (2 ): 755-766
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  • P18 peptide, a functional fragment of pigment epithelial-derived factor, inhibits angiogenesis in hepatocellular carcinoma via modulating VEGF/VEGFR2 signalling pathway #MMPMID28627623
  • Wang X ; Xiu P ; Wang F ; Zhong J ; Wei H ; Xu Z ; Liu F ; Li J
  • Oncol Rep 2017[Aug]; 38 (2 ): 755-766 PMID28627623 show ga
  • The P18 peptide is a functional fragment of pigment epithelial-derived factor (PEDF), which is an endogenic angiogenesis inhibitor. This study sought to determine the anti-angiogenic bioactivity of the P18 peptide in hepato-cellular carcinoma (HCC) and to elucidate the underlying mechanism. Xenograft tumour growth assays demonstrated the P18 peptide suppressed angiogenesis of HCC in vivo. Wound healing, Transwell and Matrigel-culture assays indicated that the P18 peptide inhibited the cell migration and tube formation of endothelial cells (ECs) in vitro. Cell viability and apoptosis assessed by Cell Counting Kit-8 (CCK-8) and ?ow cytometry assays suggested that the P18 peptide inhibited angiogenesis by inducing apoptosis of ECs. Angiogenesis- and signal transduction-associated molecules analysed by western blot demonstrated that the P18 peptide targets vascular endothelial cell growth factor receptor 2 (VEGFR2) on ECs. In conclusion, by inhibiting the phosphorylation of VEGFR2, the P18 peptide modulates signalling transduction between VEGF/VEGFR2 and suppresses activation of the PI3K/Akt cascades, leading to an increase in mitochondrial-mediated apoptosis and anti-angiogenic activity. This bioactivity of the P18 peptide may represent a novel therapeutic strategy for the treatment of HCC.
  • |Animals [MESH]
  • |Apoptosis/genetics [MESH]
  • |Carcinoma, Hepatocellular/*genetics/pathology/therapy [MESH]
  • |Cell Movement/genetics [MESH]
  • |Cell Proliferation/genetics [MESH]
  • |Cell Survival/genetics [MESH]
  • |Eye Proteins/*genetics/therapeutic use [MESH]
  • |Humans [MESH]
  • |Liver Neoplasms/*genetics/pathology/therapy [MESH]
  • |Mice [MESH]
  • |Neovascularization, Pathologic/*genetics/pathology/therapy [MESH]
  • |Nerve Growth Factors/*genetics/therapeutic use [MESH]
  • |Peptides/genetics/therapeutic use [MESH]
  • |Serpins/*genetics/therapeutic use [MESH]
  • |Signal Transduction/genetics [MESH]
  • |Vascular Endothelial Growth Factor A/*genetics [MESH]
  • |Vascular Endothelial Growth Factor Receptor-2/*genetics [MESH]
  • |Wound Healing/genetics [MESH]


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