Peptide-Drug Conjugates and Their Targets in Advanced Cancer Therapies

Paul Hoppenz1, Sylvia Els-Heindl1, Annette G Beck-Sickinger1

  • 1Faculty of Life Sciences, Institute of Biochemistry, Leipzig University, Leipzig, Germany.

Frontiers in Chemistry
|August 1, 2020
PubMed

Insights

Peptides target cancer cells by binding to overexpressed receptors, enabling targeted drug delivery. This review explores peptide-drug conjugates and advanced therapies like boron neutron capture therapy for improved cancer treatment.

Area of Science:

  • Oncology
  • Molecular Biology
  • Pharmacology

Background:

  • Cancer is a leading cause of death, with standard treatments lacking tumor selectivity and causing severe side effects.
  • Targeting cancer cells specifically while sparing healthy tissue is a major goal in cancer therapy.
  • Overexpressed cell surface receptors on cancer cells offer promising targets for selective therapies.

Purpose of the Study:

  • To review the benefits of peptides as tumor-homing agents.
  • To provide an overview of commonly targeted peptide receptors, focusing on bombesin and neuropeptide Y receptor families.
  • To outline requirements for peptide-drug conjugates (PDCs) and advanced targeted therapies.

Main Methods:

  • Literature review of peptides, receptors, and targeted cancer therapies.
  • Analysis of peptide-drug conjugate design, including linkers and drug cargos.
  • Review of boron neutron capture therapy (BNCT) developments.

Main Results:

  • Peptides can selectively target cancer cells via overexpressed receptors.
  • Peptide-drug conjugates (PDCs) offer a platform for targeted delivery of cytotoxic agents or radionuclides.
  • Boron neutron capture therapy (BNCT) represents an advanced targeted cancer treatment modality.

Conclusions:

  • Peptide-based targeting holds significant promise for selective cancer therapy.
  • Peptide-drug conjugates and advanced therapies like BNCT are crucial for improving treatment efficacy and reducing side effects.

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