Abstract | BACKGROUND AND OBJECTIVES: STUDY DESIGN/MATERIALS AND METHODS: SAS and HSC-4 cell lines were used in all the experiments. Cell viability was determined by a modified MTT assay. Two methods were used for the determination of apoptosis in human oral SCC cells: TUNEL assay and detection of fragmented mono- and oligo- nucleosomes by ELISA. Xenografts of human oral SCC cells were generated in KSN S1c nude mice. RESULTS: In vitro PDT using PAD-S31 and the 670-nm diode laser showed cytotoxicity that was a function of laser energy, drug concentration, and time to the SAS and HSC-4 cell lines. On the other hand, PAD-S31 without irradiation had no effect on cell viability. The combinated use of PAD-S31 and the laser irradiation showed excellent anti- tumor activity against tumor xenografts without severe side effects. PDT-mediated cell death occurred predominantly by apoptosis in vitro and in vivo. CONCLUSIONS: The present study demonstrates that PAD-S31 may serve as a potent photosensitizer for PDT. Furthermore, it is expected that this therapy will be clinically useful for the treatment of patients with oral carcinoma.
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Authors | Masataka Date, Isao Sakata, Kazuhide Fukuchi, Kiyoshi Ohura, Yasutaka Azuma, Mitsuko Shinohara, Koichi Matsuzaki, Yoshihisa Namiki, Hiroshi Takahashi |
Journal | Lasers in surgery and medicine
(Lasers Surg Med)
Vol. 33
Issue 1
Pg. 57-63
( 2003)
ISSN: 0196-8092 [Print] United States |
PMID | 12866122
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright 2003 Wiley-Liss, Inc. |
Chemical References |
- 13,17-bis(1-carboxypropionyl)carbamoylethyl-3-ethenyl-8-ethoxyiminoethylidene-7-hydroxy-2,7,12,18-tetramethyl porphyrin
- Photosensitizing Agents
- Porphyrins
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Topics |
- Animals
- Apoptosis
(drug effects, radiation effects)
- Carcinoma, Squamous Cell
(drug therapy, pathology)
- Cell Line, Tumor
- Disease Models, Animal
- Enzyme-Linked Immunosorbent Assay
- Humans
- In Situ Nick-End Labeling
- In Vitro Techniques
- Mice
- Mice, Nude
- Mouth Neoplasms
(drug therapy, pathology)
- Photochemotherapy
- Photosensitizing Agents
(therapeutic use)
- Porphyrins
(therapeutic use)
- Transplantation, Heterologous
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