Monitoring the effects of treatment in colon cancer cells using immunohistochemical and histoenzymatic techniques

Rom J Morphol Embryol. 2015;56(3):1103-9.

Abstract

Background: Monitoring the effects of treatment in malignant diseases is very important in study of the influence on the cell metabolism. Energy production in cancer cells is abnormally dependent on aerobic glycolysis. In addition to the dependency on glycolysis, cancer cells have other atypical metabolic characteristics. The purpose of the present study is to evaluation and analysis of the colon cancer cells under anti-angiogenic treatment, to establish the changes in the cellular energy metabolism and apoptotic potential. Anti-angiogenic drugs block the vascular endothelial growth factors, preventing the formation of new vessels.

Materials and methods: We use immunohistochemical analysis of cytochrome c release and histoenzymatic analysis of adenosine triphosphatase (ATP-ase), succinate dehydrogenase (SDH), lactate dehydrogenase (LDH) enzymes. Colorectal tumor tissue samples were obtained by biopsy following the surgical procedures at the County Clinical Hospital of Oradea (Romania).

Results: The obtained results show that the apoptotic potential of malignant cells increases during the anti-angiogenic treatment, in the same time the rate of glycolysis increases, due to installed hypoxia and reduced ATP synthesis. Our results have been confirmed by international studies too.

Conclusions: It was been demonstrated that the apoptotic potential of malignant cells increases significantly during anti-angiogenic treatment. There is growing evidence that cancer's "Achilles' heel" is tumor cell metabolism.

MeSH terms

  • Adenosine Triphosphatases / metabolism
  • Apoptosis
  • Colonic Neoplasms / drug therapy*
  • Colonic Neoplasms / metabolism
  • Colonic Neoplasms / pathology*
  • Cytochromes c / metabolism
  • Cytosol / metabolism
  • Female
  • Humans
  • Immunohistochemistry / methods*
  • L-Lactate Dehydrogenase / metabolism
  • Male
  • Middle Aged
  • Neoplasm Metastasis
  • Succinate Dehydrogenase / metabolism

Substances

  • Cytochromes c
  • L-Lactate Dehydrogenase
  • Succinate Dehydrogenase
  • Adenosine Triphosphatases