Exploring the potential impact of GLP-1 receptor agonists in cancer therapy

Baseer Aslam1, Muhammad D Bin Zafar2, Mah I Khan Changez3

  • 1Dow Medical College, Dow University of Health Sciences, Karachi, Pakistan - baseermuhammad02@gmail.com.

Minerva Endocrinology
|December 21, 2023
PubMed

Insights

Glucagon-like peptide-1 (GLP-1) receptor agonists show promise in inhibiting cancer growth and regression across various cancers. Further research is needed to overcome barriers to clinical application and optimize their use in oncology.

Area of Science:

  • Oncology
  • Endocrinology
  • Pharmacology

Background:

  • Glucagon-like peptide-1 (GLP-1) receptor agonists are established treatments for diabetes.
  • Emerging evidence suggests potential roles for GLP-1 receptor agonists in cancer therapy.

Purpose of the Study:

  • To comprehensively review the effects of GLP-1 receptor agonists on tumor suppression and regression.
  • To evaluate the potential benefits and risks of GLP-1 receptor agonists in cancer treatment.

Main Methods:

  • A comprehensive literature search was performed using Google Scholar, Scopus, and PubMed.
  • In-vitro and in-vivo studies investigating GLP-1 receptor agonists in various cancer types were analyzed.

Main Results:

  • In-vitro studies indicate GLP-1 receptor agonists inhibit cancer cell growth, induce apoptosis, and modulate angiogenesis.
  • Benefits have been observed in colon, prostate, gallbladder, ovarian, and endometrial carcinomas.
  • Concerns exist regarding potential tumorigenesis, with associations reported for liraglutide in breast, thyroid, and pancreatic cancers; however, combination therapy shows promise for pancreatic cancer.

Conclusions:

  • GLP-1 receptor agonists possess significant potential in oncology due to diverse mechanisms and favorable safety profiles.
  • Limited clinical application, awareness, and need for further research are current barriers.
  • Future research should focus on optimal dosage, patient selection, and clinical trials to integrate these agents into oncological practice.

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