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Cancer Research 68, 5291, July 1, 2008. doi: 10.1158/0008-5472.CAN-08-0222
© 2008 American Association for Cancer Research

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Experimental Therapeutics, Molecular Targets, and Chemical Biology

Pyrimethamine Induces Apoptosis of Melanoma Cells via a Caspase and Cathepsin Double-Edged Mechanism

Anna Maria Giammarioli1, Angela Maselli1, Andrea Casagrande2, Lucrezia Gambardella1, Angelo Gallina2, Massimo Spada2, Antonello Giovannetti3, Enrico Proietti2, Walter Malorni1 and Marina Pierdominici2

1 Department of Drug Research and Evaluation and 2 Department of Cell Biology and Neurosciences, Istituto Superiore di Sanità; 3 Department of Clinical Medicine, Division of Clinical Immunology, University of Rome "La Sapienza," Rome, Italy

Requests for reprints: Walter Malorni, Department of Drug Research and Evaluation, Section of Cell Aging and Degeneration, Istituto Superiore di Sanità, viale Regina Elena 299, 00161, Rome, Italy. Phone: 39-6-49902905; Fax 39-6-49903691; E-mail: malorni{at}iss.it.

Key Words: pyrimethamine • apoptosis • melanoma • caspases • cathepsin B

The unresponsiveness of metastatic melanoma to conventional chemotherapeutic and biological agents is largely due to the development of resistance to apoptosis. Pyrimethamine belongs to the group of antifolate drugs, and in addition to antiprotozoan effects, it exerts a strong proapoptotic activity, which we recently characterized in human T lymphocytes. However, no data regarding pyrimethamine anticancer activity are available thus far. To this end, we examined the in vitro effects of pyrimethamine on apoptosis, cell cycle distribution, and cell proliferation of human metastatic melanoma cell lines. The in vivo antitumor potential of pyrimethamine was evaluated in a severe combined immunodeficiency (SCID) mouse xenotransplantation model. Our data indicate that pyrimethamine, when used at a clinically relevant concentration, induced apoptosis in metastatic melanoma cells via the activation of the cathepsin B and the caspase cascade (i.e., caspase-8 and caspase-9) and subsequent mitochondrial depolarization. This occurred independently from CD95/Fas engagement. Moreover, pyrimethamine induced a marked inhibition of cell growth and an S-phase cell cycle arrest. Results obtained in SCID mice, injected s.c. with metastatic melanoma cells and treated with pyrimethamine, indicated a significant inhibitory effect on tumor growth. In conclusion, our results suggest that pyrimethamine-induced apoptosis may be considered as a multifaceted process, in which different inducers or regulators of apoptosis are simultaneously implicated, thus permitting death defects of melanoma cells to be bypassed or overcome. On these bases, we hypothesize that pyrimethamine could represent an interesting candidate for the treatment of metastatic melanoma. [Cancer Res 2008;68(13):5291–300]




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M. Chen, I. Osman, and S. J. Orlow
Antifolate Activity of Pyrimethamine Enhances Temozolomide-Induced Cytotoxicity in Melanoma Cells
Mol. Cancer Res., May 1, 2009; 7(5): 703 - 712.
[Abstract] [Full Text] [PDF]




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Copyright © 2008 by the American Association for Cancer Research.