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Showing 1–3 of 3 results
Advanced filters: Author: Kyoji Tsuchikama Clear advanced filters
  • The valine-citrulline dipeptide, which is used as a cleavable linker for antibody-drug conjugates, is instable in mouse plasma. Here, the authors developed a glutamic acid–valine–citrulline tripeptide sequence as a stable alternative that still is susceptible to cathepsin-mediated cleavage.

    • Yasuaki Anami
    • Chisato M. Yamazaki
    • Kyoji Tsuchikama
    ResearchOpen Access
    Nature Communications
    Volume: 9, P: 1-9
  • Antibody–drug conjugates (ADCs) are effective cancer drugs that have been approved for more than 20 specific indications. Nonetheless, acquired resistance and adverse events both limit the effectiveness of these agents. In this Review, the authors describe the development of novel ADC designs, including bispecific ADCs, probody–drug conjugates, immune-stimulating ADCs, protein-degrader ADCs and dual-drug ADCs. all of which have the potential to address these challenges and provide more effective ADCs.

    • Kyoji Tsuchikama
    • Yasuaki Anami
    • Chisato M. Yamazaki
    Reviews
    Nature Reviews Clinical Oncology
    Volume: 21, P: 203-223