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A short peptide derived from the antisense homology box of Fas ligand induces apoptosis in anti-Fas antibody-insensitive human ovarian cancer cells
Authors:A. Hayakawa  T. Kojima  I. Yokoyama  H. Suzuki  H. Tajiri  I. Nakashima
Affiliation:(1) Department of Equipment for Research and Education, Nagoya University, School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, 466-8550, Japan;(2) Second Department of Surgery, Nagoya University, School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, 466-8550, Japan;(3) Department of Immunology, Nagoya University, School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, 466-8550, Japan;(4) Department of Clinical Research, National Shikoku Cancer Center, 13 Horinouchi, Matsuyama, Ehime, 790-0007, Japan
Abstract:
We found that a short synthetic peptide corresponding to the ldquoantisense homology boxrdquo of Fas ligand induced apoptotic cell death of Fas-expressing human ovarian cancer cell lines. The peptide was deduced from residues 256–265 of human Fas ligand, based on the hypothesis that it should contain a specific binding site to the corresponding Fas. Interestingly, the ovarian cancer cell line NOS4, which was sensitive to anti-Fas antibody induced apoptosis, was not affected by the peptide, whereas another cell line, SKOV-3, which was insensitive to anti-Fas antibody, was killed by the peptide. Thus, this short peptide was shown to have a unique activity to induce apoptosis in human ovarian cancer cells in a manner different from anti-Fas antibody.
Keywords:Anti-Fas antibody  antisense homology box-derived peptide  apoptosis  Fas ligand  ovarian cancer.
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