Expression of emmprin (CD147), a cell surface inducer of matrix metalloproteinases, in normal human brain and gliomas

T Sameshima1, K Nabeshima, B P Toole

  • 1Department of Neurosurgery, Miyazaki Medical College, Kiyotake, Miyazaki, Japan.

Insights

Extracellular matrix metalloproteinase inducer (EMMPRIN) is more highly expressed in gliomas than normal brain tissue. EMMPRIN levels correlate with glioma malignancy, suggesting its role in astrocytoma progression.

Area of Science:

  • Neuro-oncology
  • Molecular Biology
  • Cellular Biology

Background:

  • EMMPRIN (extracellular matrix metalloproteinase inducer), also known as CD147, is an immunoglobulin superfamily member found on tumor cells.
  • EMMPRIN stimulates fibroblasts to produce matrix metalloproteinases (MMPs).
  • Homologues of EMMPRIN are involved in neuronal interactions and blood-brain barrier function.

Purpose of the Study:

  • To investigate EMMPRIN expression in human normal brain and gliomas.
  • To determine the correlation between EMMPRIN levels and glioma progression.
  • To analyze the cellular distribution of EMMPRIN in normal brain and gliomas.

Main Methods:

  • Quantitative analysis of EMMPRIN mRNA and protein expression.
  • Immunohistochemical staining for EMMPRIN localization.
  • Comparison of expression and distribution in non-neoplastic brain, low-grade astrocytoma, anaplastic astrocytoma, and glioblastoma multiforme.

Main Results:

  • EMMPRIN expression (mRNA and protein) was detected in all brain and glioma tissues.
  • Gliomas exhibited significantly higher EMMPRIN levels than non-neoplastic brain.
  • EMMPRIN expression levels and staining intensity correlated positively with glioma grade, being highest in glioblastoma multiforme.

Conclusions:

  • EMMPRIN is differentially expressed in human gliomas compared to normal brain.
  • EMMPRIN expression is associated with astrocytoma progression and malignancy.
  • The distinct cellular localization of EMMPRIN in gliomas suggests a role in tumor cell-specific functions.

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