Navigating cancer therapy: Harnessing the power of peptide-drug conjugates as precision delivery vehicles

Bulbul Sagar1, Sarthak Gupta1, Sarvesh Kumar Verma2

  • 1Department of Chemistry, Indian Institute of Technology, Delhi, 110016, New Delhi, India.

Insights

Peptide-Drug Conjugates (PDCs) offer targeted cancer treatment by delivering drugs precisely to tumors, minimizing side effects. Ongoing research aims to overcome limitations for enhanced efficacy in precision medicine.

Area of Science:

  • Oncology
  • Drug Delivery
  • Bioconjugation

Background:

  • Conventional cancer therapies like chemotherapy and radiotherapy cause significant adverse effects due to their non-selective nature.
  • Peptide-Drug Conjugates (PDCs) have emerged as a promising class of precision medicines for cancer treatment.
  • PDCs leverage the targeting capabilities of peptides to deliver cytotoxic agents directly to tumor sites.

Purpose of the Study:

  • This review focuses on the application of Peptide-Drug Conjugates (PDCs) in cancer treatment.
  • To explore the design, components, advantages, and limitations of PDCs.
  • To highlight recent advancements and future research directions in PDC development.

Main Methods:

  • Review of current literature on Peptide-Drug Conjugates in cancer therapy.
  • Analysis of PDC components: targeting ligands, cytotoxic ligands, and linkers.
  • Examination of various peptide types used in PDCs, including cell-penetrating and tumor-targeting peptides.

Main Results:

  • PDCs enhance specificity and reduce off-target effects compared to conventional therapies.
  • Targeted delivery via PDCs allows for controlled drug release, increasing efficacy and minimizing systemic toxicity.
  • PDCs utilize customized peptides to bind disease-specific receptors or biomarkers for precise accumulation in cancer cells.

Conclusions:

  • PDCs represent a significant advancement in targeted cancer therapy, offering improved therapeutic profiles.
  • Challenges such as plasma stability, rapid elimination, and limited oral bioavailability need to be addressed.
  • Further research is crucial to optimize PDC design and overcome limitations for broader clinical application.

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