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Tumour lineage-homing cell-penetrating peptides as anticancer molecular delivery systems

Author

Listed:
  • Eisaku Kondo

    (Aichi Cancer Center Research Institute
    Nagoya University Graduate School of Medicine)

  • Ken Saito

    (Aichi Cancer Center Research Institute)

  • Yuichi Tashiro

    (Okayama University Graduate School of Natural Science and Technology)

  • Kaeko Kamide

    (Mitsubishi Tanabe Pharma Corporation)

  • Shusei Uno

    (Mitsubishi Tanabe Pharma Corporation)

  • Tomoko Furuya

    (Yamaguchi University Graduate School of Medicine)

  • Masao Mashita

    (Sigma-Aldrich Japan Corporation)

  • Kiichiro Nakajima

    (KNC Laboratories Co. Ltd.)

  • Tomoyuki Tsumuraya

    (Graduate School of Medicine, University of the Ryukyus)

  • Naoya Kobayashi

    (Okayama Saidaiji Hospital)

  • Masahiro Nishibori

    (Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences)

  • Mitsune Tanimoto

    (Oncology and Respiratory Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences)

  • Masayuki Matsushita

    (Graduate School of Medicine, University of the Ryukyus)

Abstract

Cell-penetrating peptides have gained attention owing to their promise in noninvasive delivery systems. Among the identified cell-penetrating peptides, the TAT peptide has been preferentially used for transduction into cells of diverse origins. However, this activity is nonselective between neoplastic and non-neoplastic cells. Here we describe artificial cell-penetrating peptides that are selectively and efficiently incorporated into human tumour cells, according to their lineage. Ten representative tumour lineage-homing cell-penetrating peptides were obtained by screening of a random peptide library constructed using messenger RNA display technology, and some of the isolates were further modified by amino-acid substitution. Their advantageous tumour cell-targeting ability is corroborated in an in vivo mouse model for imaging and growth suppression of metastatic xenoplant tumours. These cell-penetrating peptides are potentially useful for the efficient targeting of human neoplasms in a tumour origin-dependent manner, and provide a framework for the development of peptide-based anti-tumour technologies.

Suggested Citation

  • Eisaku Kondo & Ken Saito & Yuichi Tashiro & Kaeko Kamide & Shusei Uno & Tomoko Furuya & Masao Mashita & Kiichiro Nakajima & Tomoyuki Tsumuraya & Naoya Kobayashi & Masahiro Nishibori & Mitsune Tanimoto, 2012. "Tumour lineage-homing cell-penetrating peptides as anticancer molecular delivery systems," Nature Communications, Nature, vol. 3(1), pages 1-13, January.
  • Handle: RePEc:nat:natcom:v:3:y:2012:i:1:d:10.1038_ncomms1952
    DOI: 10.1038/ncomms1952
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    Cited by:

    1. Yuki Yamanashi & Shinpei Takamaru & Atsushi Okabe & Satoshi Kaito & Yuto Azumaya & Yugo R. Kamimura & Kenzo Yamatsugu & Tomoya Kujirai & Hitoshi Kurumizaka & Atsushi Iwama & Atsushi Kaneda & Shigehiro, 2025. "Chemical catalyst manipulating cancer epigenome and transcription," Nature Communications, Nature, vol. 16(1), pages 1-15, December.

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