Antitumoral effect of Ocoxin on acute myeloid leukemia
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Elena Díaz-Rodríguez1, Susana Hernández-García1, Eduardo Sanz2, Atanasio Pandiella1
1Instituto de Biología Molecular y Celular del Cáncer CSIC-Universidad de Salamanca, Salamanca, Spain
2Catalysis, S.L., Madrid, Spain
Atanasio Pandiella, e-mail: firstname.lastname@example.org
Keywords: acute myeloid leukemia, antioxidants, cell cycle, p27
Received: November 19, 2015 Accepted: December 22, 2015 Published: January 09, 2016
Acute myeloid leukemia (AML) is a heterogeneous hematological malignancy whose incidence is growing in developed countries. In the relapse setting, very limited therapeutic options are available and in most cases only palliative care can be offered to patients. The effect of a composite formulation that contains several antioxidants, Ocoxin Oral solution (OOS), was tested in this condition. When analyzed in vitro, OOS exhibited anti-AML action that was both time and dose dependent. In vivo OOS induced a ralentization of tumor growth that was due to a decrease in cell proliferation. Such effect could, at least partially, be due to an increase in the cell cycle inhibitor p27, although other cell cycle proteins seemed to be altered. Besides, OOS induced an immunomodulatory effect through the induction of IL6. When tested in combination with other therapeutic agents normally used in the treatment of AML patients, OOS demonstrated a higher antiproliferative action, suggesting that it may be used in combination with those standard of care treatments to potentiate their antiproliferative action in the AML clinic.
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