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1 March 2006 Potentiation of the Antitumor Effect of Merocyanine 540–mediated Photodynamic Therapy by Amifostine and Amphotericin B
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Abstract

Leukemia and lymphoma cells are much more sensitive to Merocyanine 540 (MC540)–mediated photodynamic therapy (PDT) than normal pluripotent hematopoietic stem cells and normal colony forming unit–granulocyte/macrophage progenitors (CFU-GM). By contrast, most solid tumor cells are only moderately sensitive to MC540-PDT. The limited activity against solid tumor cells has detracted from MC540's appeal as a broad-spectrum purging agent. We report here that noncytotoxic concentrations of amifostine (Ethyol, Ethiofos, WR-2721) and amphotericin B used either alone or in combination potentiate the MC540-sensitized photoinactivation of leukemia cells, wild-type small cell lung cancer cells and cisplatin-resistant small cell lung cancer cells. Amphotericin B also enhances the MC540-sensitized photoinactivation of normal CFU-GM, whereas amifostine protects CFU-GM against the cytotoxic action of MC540-PDT. The yield of CD34-positive normal hematopoietic stem and progenitor cells is only minimally diminished by pretreatment with amifostine, amphotericin B or combinations of amifostine plus amphotericin B. Purging protocols that combine MC540-PDT with amifostine or with amifostine plus amphotericin B could offer a simple and effective approach to the purging of autologous stem cell grafts that are contaminated with solid tumor cells or the purging of stem cell grafts from heavily pretreated leukemia patients that contain reduced numbers of normal stem and progenitor cells and, therefore, can ill afford additional losses caused by purging.

Ichiro Tsujino, Kiyoko Miyagi, Reynée W. Sampson, and Fritz Sieber "Potentiation of the Antitumor Effect of Merocyanine 540–mediated Photodynamic Therapy by Amifostine and Amphotericin B," Photochemistry and Photobiology 82(2), 458-465, (1 March 2006). https://doi.org/10.1562/2005-09-02-RA-672
Received: 2 September 2005; Accepted: 1 October 2005; Published: 1 March 2006
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