The ultrastructural study of tumorigenic cells using nanobiomarkers

Cancer Biother Radiopharm. 2010 Jun;25(3):289-98. doi: 10.1089/cbr.2009.0697.

Abstract

Despite recent advances, patients with malignant brain tumors still have a poor prognosis. Glioblastoma (WHO grade 4 astrocytoma), the most malignant brain tumor, represents 50% of all astrocytomas, with a median survival rate of <1 year. It is, therefore, extremely important to search for new diagnostic and therapeutic approaches for patients with glioblastoma. This study describes the application of superparamagnetic nanoparticles of iron oxide, as well as monoclonal antibodies, of immunophenotypic significance, conjoined to quantum dots for the ultrastructural assessment of glioblastoma cells. For this proposal, an immunophenotypic study by flow cytometry was carried out, followed by transmission electron microscopy analysis. The process of tumor cell labeling using nanoparticles can successfully contribute to the identification of tumorigenic cells and consequently for better understanding of glioblastoma genesis and recurrence. In addition, this method may help further studies in tumor imaging, diagnosis, and prognostic markers detection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AC133 Antigen
  • Antibodies, Monoclonal / chemistry
  • Antibodies, Monoclonal / immunology
  • Antibodies, Monoclonal / metabolism
  • Antigens, CD / immunology
  • Antigens, CD / metabolism
  • Biomarkers / analysis
  • Biomarkers / chemistry
  • Cell Line, Tumor
  • Cell Membrane / metabolism
  • Cell Nucleus / metabolism
  • Cytoplasm / metabolism
  • Cytoplasmic Vesicles / metabolism
  • Endocytosis / immunology
  • Endoglin
  • Flow Cytometry
  • Forkhead Box Protein M1
  • Forkhead Transcription Factors / chemistry
  • Forkhead Transcription Factors / metabolism
  • Glioblastoma / diagnosis*
  • Glioblastoma / metabolism
  • Glioblastoma / ultrastructure*
  • Glycoproteins / immunology
  • Glycoproteins / metabolism
  • Humans
  • Hyaluronan Receptors / immunology
  • Hyaluronan Receptors / metabolism
  • Immunophenotyping
  • Integrin beta1 / immunology
  • Integrin beta1 / metabolism
  • Magnetite Nanoparticles / chemistry
  • Microscopy, Electron, Transmission
  • Nanomedicine / methods
  • Nanoparticles* / chemistry
  • Peptides / immunology
  • Peptides / metabolism
  • Quantum Dots
  • Receptors, Cell Surface / immunology
  • Receptors, Cell Surface / metabolism
  • Staining and Labeling / methods*
  • Tumor Cells, Cultured

Substances

  • AC133 Antigen
  • Antibodies, Monoclonal
  • Antigens, CD
  • Biomarkers
  • CD44 protein, human
  • ENG protein, human
  • Endoglin
  • FOXM1 protein, human
  • Forkhead Box Protein M1
  • Forkhead Transcription Factors
  • Glycoproteins
  • Hyaluronan Receptors
  • Integrin beta1
  • Magnetite Nanoparticles
  • Peptides
  • Receptors, Cell Surface