Peptide Drugs in Gastrointestinal Tumors: Integrating Targeting, Delivery, and Therapeutic Actions for Synergistic

Qian Ouyang1,2, Guifang Wu1,2, Anyi Chen1,2

  • 1National "111" Center for Cellular Regulation and Molecular Pharmaceutics, Hubei University of Technology, Wuhan 430068, China.

Biomolecules
|March 28, 2026
PubMed

Insights

Peptide drugs show promise for treating gastrointestinal tumors by targeting cancer cells specifically. This review explores their mechanisms, delivery, and potential for improved cancer therapy.

Area of Science:

  • Oncology
  • Drug Discovery
  • Biotechnology

Background:

  • Gastrointestinal (GI) cancers cause significant mortality globally.
  • Current treatments like chemotherapy and radiotherapy have limitations due to side effects and resistance.
  • Novel, targeted therapies are crucial for improving patient outcomes.

Purpose of the Study:

  • To review the advancements in peptide drug development for GI malignancies.
  • To highlight the molecular mechanisms, delivery strategies, and applications of peptide drugs.
  • To discuss challenges and future directions for clinical translation.

Main Methods:

  • Systematic review of current research on peptide drugs in GI oncology.
  • Analysis of molecular mechanisms of peptide-based antitumor effects.
  • Evaluation of delivery modification strategies for enhanced efficacy.
  • Summary of recent clinical applications and preclinical studies.

Main Results:

  • Peptide drugs offer high specificity, biocompatibility, and low immunogenicity.
  • They can precisely target tumor receptors and interfere with cancer cell signaling pathways.
  • Peptide drugs demonstrate multi-target antitumor effects, including direct cytotoxicity and immune modulation.
  • Various delivery systems are being developed to improve peptide drug stability and tumor penetration.

Conclusions:

  • Peptide drugs represent a promising therapeutic strategy for gastrointestinal tumors.
  • Further research into molecular mechanisms and delivery systems is needed.
  • Clinical translation requires addressing challenges in stability, immunogenicity, and manufacturing.

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