Migration-inducing gene-7 independently predicts poor prognosis of human osteosarcoma and is associated with vasculogenic mimicry

Exp Cell Res. 2018 Aug 1;369(1):80-89. doi: 10.1016/j.yexcr.2018.05.008. Epub 2018 May 8.

Abstract

Vasculogenic mimicry (VM) is a special type of vascular channel formed by tumor cells without endothelial cell participation. Migration-inducing gene 7 (MIG-7) plays an important role in regulating VM. In this study, immunohistochemical staining was used to detect MIG-7 in tissue specimens from 141 primary osteosarcoma patients, and the relationship between MIG-7 and VM was examined. Survival analysis were performed to evaluate the prognoses. MIG-7 knockdown osteosarcoma cells were used for cell proliferation, apoptosis, migration, invasiveness and VM formation assays. A spontaneously metastasizing cell line-derived orthotopic xenograft mouse model was established to evaluate the effect of MIG-7 knockdown on tumorigenesis, VM formation and lung metastasis. MIG-7 expression was associated with VM formation. There were significant differences in overall and metastasis-free survival between the MIG-7-positive and MIG-7-negative groups. The MIG-7 expression was shown to be an independent indicator of both overall and metastasis-free survival. In vitro knockdown of MIG-7 dramatically reduced migration, invasion and VM formation in osteosarcoma cells without any significant effect on cell proliferation and apoptosis. MIG-7 knockdown also exhibited potent antitumor, antimetastasis and anti-VM effects in the orthotopic mouse model of 143B osteosarcoma. Therefore, MIG-7 serves as an independent unfavorable prognostic indicator in osteosarcoma patients and MIG-7 is an important mediator of osteosarcoma VM formation.

Keywords: Metastasis; Migration-inducing gene-7; Osteosarcoma; Prognosis; Vasculogenic mimicry.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Animals
  • Biological Mimicry / genetics*
  • Biological Mimicry / physiology
  • Biomarkers, Tumor / genetics
  • Biomarkers, Tumor / physiology*
  • Bone Neoplasms / diagnosis*
  • Bone Neoplasms / genetics
  • Bone Neoplasms / mortality
  • Bone Neoplasms / pathology
  • Child
  • Child, Preschool
  • Disease Progression
  • Female
  • HEK293 Cells
  • Humans
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Middle Aged
  • Neoplasm Metastasis
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / physiology*
  • Neovascularization, Pathologic / diagnosis
  • Neovascularization, Pathologic / genetics*
  • Neovascularization, Pathologic / pathology
  • Osteosarcoma / diagnosis*
  • Osteosarcoma / genetics
  • Osteosarcoma / mortality
  • Osteosarcoma / pathology
  • Prognosis
  • Survival Analysis
  • Tumor Cells, Cultured
  • Young Adult

Substances

  • Biomarkers, Tumor
  • Neoplasm Proteins
  • TOX4 protein, human