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MIG7 is involved in vasculogenic mimicry formation rendering invasion and metastasis in hepatocellular carcinoma.

Oncol. Rep.2018 Feb;39(2):679-686. doi:10.3892/or.2017.6138. Epub 2017 Dec 07
Bo Qu 1 , Guannan Sheng 2 , Long Guo 3 , Fei Yu 2 , Guannan Chen 2 , Qi Lu 4 , Renjie Wang 5 , Bing Han 3 , Yi Lu 3
Bo Qu 1 , Guannan Sheng 2 , Long Guo 3 , Fei Yu 2 , Guannan Chen 2 , Qi Lu 4 , Renjie Wang 5 , Bing Han 3 , Yi Lu 3
+ et al

[No authors listed]

Author information
  • 1 Department of Oncological Surgery, Affiliated Hospital of the Logistics University of Chinese People's Armed Police Forces, Tianjin 300162, P.R. China.
  • 2 Department of Oncological Surgery, Postgraduate Training Basement of Jinzhou Medical University in the Affiliated Hospital of the Logistics University of Chinese People's Armed Police Forces, Tianjin 300162, P.R. China.
  • 3 Department of Hepatobiliary Surgery, The First Affiliated Hospital of Medical College, Xi'an Jiaotong University, Xi'an, Shaanxi 710061, P.R. China.
  • 4 Institute of Disaster Medicine and Public Health, Affiliated Hospital of the Logistic University of Chinese People's Armed Police Force, Tianjin 300162, P.R. China.
  • 5 Department of clinical Laboratory, Affiliated Hospital of the Logistics University of Chinese People's Armed Police Forces, Tianjin 300162, P.R. China.

摘要


Migration-inducing gene 7 (MIG7) is highly expressed and is implicated in multiple malignant tumors with vasculogenic mimicry (VM) which renders possible routes without the endothelium for invasion and metastasis. However, there are few reports in the literature describing the relationship between MIG7 expression and VM formation in hepatocellular carcinoma (HCC). In the present study, we found a significantly positive correlation between MIG7 expression and VM in 40 HCC specimens. Three-dimensional (3D) culture showed that VM formation in the HCC cell line MHCC-97H with high metastatic potential was enhanced to a greater extent than that of MHCC-97L and Huh-7 with low and non-metastatic potential. There was no VM formation in human normal hepatocyte line L-02. Moreover, MIG7 expression was higher in MHCC-97H than in MHCC-97L and Huh-7 cells and non-detectable in L-02 cells. MIG7 knockdown in MHCC-97H cells reduced VM formation, and weakened the invasive properties accompanying the enhanced cellular adhesion. Notably, there was no significant effect of endostatin (ES), a broad-spectrum angiogenesis inhibitor applied to clinical treatment, on both MIG7 expression and VM formation. Thus, the present study presents a causal link between MIG7 expression and VM formation in HCC, suggesting a potential treatment target for invasion and metastasis.