Oral Oncology
Volume 38, Issue 4 , Pages 343-348, June 2002

Analysis of fluorescence in oral squamous cell carcinoma

  • Kojiro Onizawa

      Affiliations

    • Department of Oral and Maxillofacial Surgery, Institute of Clinical Medicine, University of Tsukuba, 1-1-1 Tennodai, Tsukuba-shi, Ibaraki-ken 305-8575, Japan
    • Corresponding Author InformationCorresponding author. Tel.: +81-298-53-3052; fax: +81-298-53-3039
  • ,
  • Naomichi Okamura

      Affiliations

    • College of Medical Technology and Nursing, University of Tsukuba, Japan
  • ,
  • Hideo Saginoya

      Affiliations

    • Medical Photo-studio, University of Tsukuba Hospital, Japan
  • ,
  • Hiroshi Yusa

      Affiliations

    • Department of Oral and Maxillofacial Surgery, Institute of Clinical Medicine, University of Tsukuba, 1-1-1 Tennodai, Tsukuba-shi, Ibaraki-ken 305-8575, Japan
  • ,
  • Toru Yanagawa

      Affiliations

    • Department of Oral and Maxillofacial Surgery, Institute of Clinical Medicine, University of Tsukuba, 1-1-1 Tennodai, Tsukuba-shi, Ibaraki-ken 305-8575, Japan
  • ,
  • Hiroshi Yoshida

      Affiliations

    • Department of Oral and Maxillofacial Surgery, Institute of Clinical Medicine, University of Tsukuba, 1-1-1 Tennodai, Tsukuba-shi, Ibaraki-ken 305-8575, Japan

Received 8 February 2001; received in revised form 19 March 2001; accepted 11 June 2001.

Abstract 

This study was carried out to examine the spectral properties of the red fluorescence emitted from oral squamous cell carcinoma (SCC). Fluorescent samples obtained from oral cancers induced in hamsters, human oral SCCs, and the medium from cultured oral cancer cell lines were analyzed with a spectrofluorometer with excitation at 404 nm. The spectral profile of the experimentally induced cancers changed with increasing malignancy: peaks at 634 and 672 nm increased and peaks at 520 and 582 nm decreased. A reduction in fluorescence intensity at 582 nm and a rise of intensity at 634 nm were commonly observed in the experimental, clinical, and cell line samples, and the ratio of the fluorescence intensity at 582 nm over that at 634 nm was consistent in all samples. These results suggested that the red fluorescence was emitted by porphyrin, which we believe to be produced by oral SCCs and to accumulate inside or on the surface of cancer tissues in greater amounts with progressing malignancy.

Keywords:  Oral cancer, Autofluorescence, Porphyrin, Fluorescence photography

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PII: S1368-8375(01)00070-7

Oral Oncology
Volume 38, Issue 4 , Pages 343-348, June 2002