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Development of pro-apoptotic peptides as potential therapy for peritoneal endometriosis

Author

Listed:
  • K. Sugihara

    (Hamamatsu University School of Medicine)

  • Y. Kobayashi

    (Tumor Microenvironment, Cancer Center, Sanford-Burnham Medical Research Institute)

  • A. Suzuki

    (Keio University School of Medicine)

  • N. Tamura

    (Tumor Microenvironment, Cancer Center, Sanford-Burnham Medical Research Institute)

  • K. Motamedchaboki

    (Tumor Microenvironment, Cancer Center, Sanford-Burnham Medical Research Institute)

  • C.-T. Huang

    (Tumor Microenvironment, Cancer Center, Sanford-Burnham Medical Research Institute)

  • T.O. Akama

    (Tumor Microenvironment, Cancer Center, Sanford-Burnham Medical Research Institute)

  • J. Pecotte

    (Southwest National Primate Research Center, Texas Biomedical Research Institute)

  • P. Frost

    (Southwest National Primate Research Center, Texas Biomedical Research Institute)

  • C. Bauer

    (Southwest National Primate Research Center, Texas Biomedical Research Institute)

  • J.B. Jimenez

    (Southwest National Primate Research Center, Texas Biomedical Research Institute)

  • J. Nakayama

    (Shinshu University Graduate School of Medicine)

  • D. Aoki

    (Keio University School of Medicine)

  • M.N. Fukuda

    (Tumor Microenvironment, Cancer Center, Sanford-Burnham Medical Research Institute)

Abstract

Endometriosis is a common gynaecological disease associated with pelvic pain and infertility. Current treatments include oral contraceptives combined with nonsteroidal anti-inflammatory drugs or surgery to remove lesions, all of which provide a temporary but not complete cure. Here we identify an endometriosis-targeting peptide that is internalized by cells, designated z13, using phage display. As most endometriosis occurs on organ surfaces facing the peritoneum, we subtracted a phage display library with female mouse peritoneum tissue and selected phage clones by binding to human endometrial epithelial cells. Proteomics analysis revealed the z13 receptor as the cyclic nucleotide-gated channel β3, a sorting pathway protein. We then linked z13 with an apoptosis-inducing peptide and with an endosome-escaping peptide. When these peptides were co-administered into the peritoneum of baboons with endometriosis, cells in lesions selectively underwent apoptosis with no effect on neighbouring organs. Thus, this study presents a strategy that could be useful to treat peritoneal endometriosis in humans.

Suggested Citation

  • K. Sugihara & Y. Kobayashi & A. Suzuki & N. Tamura & K. Motamedchaboki & C.-T. Huang & T.O. Akama & J. Pecotte & P. Frost & C. Bauer & J.B. Jimenez & J. Nakayama & D. Aoki & M.N. Fukuda, 2014. "Development of pro-apoptotic peptides as potential therapy for peritoneal endometriosis," Nature Communications, Nature, vol. 5(1), pages 1-9, December.
  • Handle: RePEc:nat:natcom:v:5:y:2014:i:1:d:10.1038_ncomms5478
    DOI: 10.1038/ncomms5478
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