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Photodynamic Therapy Mediated by a Novel Chlorin Derivative, TONS 501-Na, in EMT6 cells.
Osaki, Tomohiro; Sakata, Isao; Uto, Yoshihiro; Azuma, Kazuo; Murahata, Yusuke; Tsuka, Takeshi; Itoh, Norihiko; Imagawa, Tomohiro; Okamoto, Yoshiharu.
Afiliación
  • Osaki T; Department of Veterinary Clinical Medicine, School of Veterinary Medicine, Tottori University, Tottori, Japan tosaki@muses.tottori-u.ac.jp.
  • Sakata I; Porphyrin Laboratory, Okayama, Japan.
  • Uto Y; Faculty of Bioscience and Bioindustry, Tokushima University, Tokushima, Japan.
  • Azuma K; Department of Veterinary Clinical Medicine, School of Veterinary Medicine, Tottori University, Tottori, Japan.
  • Murahata Y; Department of Veterinary Clinical Medicine, School of Veterinary Medicine, Tottori University, Tottori, Japan.
  • Tsuka T; Department of Veterinary Clinical Medicine, School of Veterinary Medicine, Tottori University, Tottori, Japan.
  • Itoh N; Department of Veterinary Clinical Medicine, School of Veterinary Medicine, Tottori University, Tottori, Japan.
  • Imagawa T; Department of Veterinary Clinical Medicine, School of Veterinary Medicine, Tottori University, Tottori, Japan.
  • Okamoto Y; Department of Veterinary Clinical Medicine, School of Veterinary Medicine, Tottori University, Tottori, Japan.
Anticancer Res ; 37(4): 1723-1728, 2017 04.
Article en En | MEDLINE | ID: mdl-28373434
ABSTRACT

BACKGROUND:

The lipophilic photosensitizer, TONS 501, is a novel porphyrin-derived methyl ester that was developed for photodynamic antimicrobial chemotherapy. This study developed a hydrophilic and anionic porphyrin salt of this compound (TONS 501-Na) for use in photodynamic therapy (PDT). This chlorin derivative is synthesized from the protoporphyrin IX dimethyl ester. MATERIALS AND

METHODS:

We investigated the in vitro cytotoxic effects of TONS 501-Na-mediated PDT on EMT6 mouse breast cancer cells. EMT6 cells were incubated with 0-100 µg/ml TONS 501-Na for 24 h prior to replacing the culture medium and exposing the cells to 6 mW/cm2 diode laser irradiation at 0-13 J/cm2 to induce PDT. Morphological changes and cell viability were evaluated 24 h after PDT. The percentages of apoptotic cells were evaluated 4 h and 24 h after PDT.

RESULTS:

The concentrations of TONS 501-Na that killed 50% of EMT6 cells after exposure to light doses of 0, 0.4, 3, 6, or 13 J/cm2 were 84.6, 33.2, 18, 8.2, and 2.2 µg/ml, respectively. Tumor cells exposed to PDT showed chromatin condensation and fragmentation. The percentages of apoptotic cells increased in a TONS 501-Na concentration-dependent manner in the PDT group, and were significantly higher than those in the control group or in cells treated with TONS 501-Na or laser irradiation alone.

CONCLUSION:

TONS 501-Na-mediated PDT induced mouse breast cancer cell death in a concentration-dependent manner. Future studies should evaluate the in vivo pharmacokinetics, tissue distribution, and photodynamic effects of TONS 501-Na.
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fotoquimioterapia / Porfirinas / Neoplasias Mamarias Animales / Fármacos Fotosensibilizantes / Apoptosis / Luz Límite: Animals Idioma: En Revista: Anticancer Res Año: 2017 Tipo del documento: Article País de afiliación: Japón
Buscar en Google
Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fotoquimioterapia / Porfirinas / Neoplasias Mamarias Animales / Fármacos Fotosensibilizantes / Apoptosis / Luz Límite: Animals Idioma: En Revista: Anticancer Res Año: 2017 Tipo del documento: Article País de afiliación: Japón
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