Ecto-5'-Nucleotidase Overexpression Reduces Tumor Growth in a Xenograph Medulloblastoma Model

PLoS One. 2015 Oct 22;10(10):e0140996. doi: 10.1371/journal.pone.0140996. eCollection 2015.

Abstract

Background: Ecto-5'-nucleotidase/CD73 (ecto-5'-NT) participates in extracellular ATP catabolism by converting adenosine monophosphate (AMP) into adenosine. This enzyme affects the progression and invasiveness of different tumors. Furthermore, the expression of ecto-5'-NT has also been suggested as a favorable prognostic marker, attributing to this enzyme contradictory functions in cancer. Medulloblastoma (MB) is the most common brain tumor of the cerebellum and affects mainly children.

Materials and methods: The effects of ecto-5'-NT overexpression on human MB tumor growth were studied in an in vivo model. Balb/c immunodeficient (nude) 6 to 14-week-old mice were used for dorsal subcutaneous xenograph tumor implant. Tumor development was evaluated by pathophysiological analysis. In addition, the expression patterns of adenosine receptors were verified.

Results: The human MB cell line D283, transfected with ecto-5'-NT (D283hCD73), revealed reduced tumor growth compared to the original cell line transfected with an empty vector. D283hCD73 generated tumors with a reduced proliferative index, lower vascularization, the presence of differentiated cells and increased active caspase-3 expression. Prominent A1 adenosine receptor expression rates were detected in MB cells overexpressing ecto-5'-NT.

Conclusion: This work suggests that ecto-5'-NT promotes reduced tumor growth to reduce cell proliferation and vascularization, promote higher differentiation rates and initiate apoptosis, supposedly by accumulating adenosine, which then acts through A1 adenosine receptors. Therefore, ecto-5'-NT might be considered an important prognostic marker, being associated with good prognosis and used as a potential target for therapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 5'-Nucleotidase / genetics
  • 5'-Nucleotidase / metabolism*
  • Adenosine Monophosphate / metabolism
  • Animals
  • Cell Line, Tumor
  • Cell Proliferation / genetics
  • Cell Proliferation / physiology
  • Humans
  • Medulloblastoma / enzymology*
  • Medulloblastoma / genetics
  • Medulloblastoma / therapy*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Receptor, Adenosine A1 / metabolism
  • Xenograft Model Antitumor Assays

Substances

  • Receptor, Adenosine A1
  • Adenosine Monophosphate
  • 5'-Nucleotidase

Grants and funding

This work was supported by Fundação de Amparo à Pesquisa do Estado de São Paulo - FAPESP (Proc. 2012/50880-4); Conselho Nacional de Desenvolvimento Científico e Tecnológico - CNPq (Proc. 303016/2009-4); and Fundo de Incentivo a Pesquisa e Eventos - FIPE/HCPA (Proc. 10-0132). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.