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10.18632/oncotarget.6672

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suck abstract from ncbi


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pmid26848615
      Oncotarget 2016 ; 7 (8 ): 9525-37
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  • The Notch pathway promotes the cancer stem cell characteristics of CD90+ cells in hepatocellular carcinoma #MMPMID26848615
  • Luo J ; Wang P ; Wang R ; Wang J ; Liu M ; Xiong S ; Li Y ; Cheng B
  • Oncotarget 2016[Feb]; 7 (8 ): 9525-37 PMID26848615 show ga
  • CD90 has been identified as a marker for liver cancer stem cells (CSCs) that are responsible for tumorigenic activity, but it is not known how CD90+ cells contribute to tumor initiation and progression. Our data demonstrated that high expression of CD90 in Hepatocellular Carcinoma (HCC) tissues correlated with venous filtration in HCC patients. CD90+ cells isolated from HCC cell lines exhibited increased tumorigenicity, chemoresistance, tumor invasion and metastasis. Notch pathway was activated in CD90+ cells and we found that inhibition of Notch pathway in CD90+ CSCs decreased tumorigenicity, cell invasion, migration and expression of stem cell related genes. Activation of Notch pathway in CD90- cells induced self-renewal, invasion and migration. Furthermore, we observed that cancer stem cell features were facilitated by stimulating G1-S transition in the cell cycle phase and inhibiting apoptosis mediated by Notch pathway. Our findings suggested CD90 could be used as a potential biomarker for HCC CSCs, and that cancer stem cell activity was elevated through up activated Notch pathway in CD90+ CSCs.
  • |Animals [MESH]
  • |Apoptosis [MESH]
  • |Biomarkers, Tumor [MESH]
  • |Carcinoma, Hepatocellular/metabolism/*pathology [MESH]
  • |Cell Line, Tumor [MESH]
  • |Drug Resistance, Neoplasm [MESH]
  • |Humans [MESH]
  • |Liver Neoplasms/metabolism/*pathology [MESH]
  • |Male [MESH]
  • |Mice [MESH]
  • |Mice, Inbred NOD [MESH]
  • |Mice, SCID [MESH]
  • |Neoplasm Invasiveness/pathology [MESH]
  • |Neoplasm Metastasis/pathology [MESH]
  • |Neoplastic Stem Cells/*pathology [MESH]
  • |Receptors, Notch/antagonists & inhibitors/*metabolism [MESH]


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