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Photodynamic therapy with ATX-S10.Na(II) inhibits synovial sarcoma cell growth.

Abstract
Photodynamic therapy (PDT) is an effective cancer treatment modality that allows selective destruction of malignant tumor cells. We asked whether PDT could inhibit in vivo and in vitro growth of synovial sarcoma cells. We analyzed PDT using ATX-S10.Na(II) and a diode laser for a synovial sarcoma cell line (SYO-1). Photodynamic therapy with ATX-S10.Na(II) showed an in vitro cytotoxic effect on the cultured SYO-1 cells. The in vitro effect of PDT depended on the treatment concentration of ATX-S10.Na(II) and the laser dose of irradiation. ATX-S10.Na(II) was detected in the tumor tissue specimens that were excised from nude mice bearing SYO-1 within 6 hours after intravenous injection, but it was eliminated from the tumor 12 hours after injection. Photodynamic therapy suppressed the tumor growth of nude mice bearing SYO-1, and high-dose irradiation induced no viable tumor cells in histologic specimens. Photodynamic therapy performed after marginal resection of the tumor of nude mice bearing SYO-1 reduced the rate of local recurrence of the tumor. Our results suggest PDT using ATX-S10.Na(II) and laser irradiation may be a potentially useful treatment for synovial sarcoma, especially to reduce the surgical margin and preserve critical anatomic structures adjacent to the tumor.
AuthorsKen Takeda, Toshiyuki Kunisada, Shinichi Miyazawa, Yoshinori Nakae, Toshifumi Ozaki
JournalClinical orthopaedics and related research (Clin Orthop Relat Res) Vol. 466 Issue 7 Pg. 1726-33 (Jul 2008) ISSN: 1528-1132 [Electronic] United States
PMID18465181 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • ATX-S10
  • Photosensitizing Agents
  • Porphyrins
Topics
  • Animals
  • Cell Line, Tumor
  • Cell Proliferation (radiation effects)
  • Disease Models, Animal
  • Mice
  • Mice, Nude
  • Photochemotherapy
  • Photosensitizing Agents (therapeutic use)
  • Porphyrins (therapeutic use)
  • Sarcoma, Synovial (drug therapy)
  • Xenograft Model Antitumor Assays

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