Effect of GLP-1 receptor agonists on prostate cancer risk reduction: a systematic review and meta-analysis

Nikhil Sharma1, Mahalaqua Nazli Khatib2, Ashok Kumar Balaraman3

  • 1Department of Pharmacy Practice, National Institute of Pharmaceutical Education and Research, Guwahati, 781101, India.

PubMed
Abstract

Insights

Glucagon-like peptide 1 receptor agonists (GLP-1 RAs) show a 28% reduced risk of prostate cancer in men, particularly those with type 2 diabetes mellitus. This suggests GLP-1 RAs may help mitigate cancer risk alongside diabetes management.

Area of Science:

  • Oncology
  • Endocrinology
  • Pharmacology

Background:

  • Prostate cancer is a leading global malignancy in men.
  • Glucagon-like peptide 1 receptor agonists (GLP-1 RAs) are key treatments for type 2 diabetes mellitus (T2DM).
  • Emerging research explores GLP-1 RAs' impact on cancer risk.

Purpose of the Study:

  • To systematically review and meta-analyze the association between GLP-1 RA use and prostate cancer risk reduction.
  • To evaluate the efficacy of GLP-1 RAs in mitigating prostate cancer incidence.

Main Methods:

  • Comprehensive literature search of PubMed, Embase, and Web of Science up to July 30, 2024.
  • Inclusion of randomized controlled trials, cohort, case-control, and observational studies.
  • Quality assessment using Newcastle-Ottawa Scale and Cochrane Risk of Bias tool; meta-analysis with a random effects model.

Main Results:

  • Five studies analyzed, revealing reduced prostate cancer risk with GLP-1 RA use.
  • Meta-analysis showed a statistically significant 28% reduction in prostate cancer risk (RR 0.72; 95% CI: 0.610 to 0.832).
  • Moderate heterogeneity (I²=51%) observed; sensitivity analysis confirmed findings.

Conclusions:

  • GLP-1 RA use is significantly associated with reduced prostate cancer risk in men, especially those with T2DM.
  • GLP-1 RAs show potential as a cancer risk mitigation strategy beyond diabetes management.
  • Further research is needed to explore mechanisms, optimal dosages, and therapy durations.

Related Concept Videos

Glucagon-like Receptor Agonists01:24

Glucagon-like Receptor Agonists

Incretins include glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP), which stimulate insulin secretion post-meals. In type 2 diabetes, GIP's efficacy is reduced, making GLP-1 a viable drug target. GIP originates from preproGIP.
GLP-1, when administered in high doses intravenously, triggers insulin secretion, inhibits glucagon release, slows gastric emptying, reduces food intake, and restores normal insulin secretion. However, its rapid inactivation by...
300
Dipeptidyl Peptidase 4 Inhibitors01:23

Dipeptidyl Peptidase 4 Inhibitors

Dipeptidyl peptidase 4 (DPP-4) is a serine protease widely distributed in the body. It's involved in the inactivation of GLP-1 and GIP hormones, which are crucial for insulin regulation. DPP-4 inhibitors, such as sitagliptin (Januvia), saxagliptin (Onglyza), linagliptin (Tradjenta), alogliptin (Nesina), and vildagliptin (Galvus), help increase the proportion of active GLP-1, enhancing insulin secretion. These inhibitors work by competitively binding to DPP-4. This binding causes a...
172
Oral Hypoglycemic Agents: Biguanides and Glitazones01:26

Oral Hypoglycemic Agents: Biguanides and Glitazones

Biguanides, particularly metformin (Glucophage), are insulin sensitizers that enhance glucose uptake, thereby reducing insulin resistance. Unlike sulfonylureas, metformin doesn't prompt insulin secretion, which helps to curb hypoglycemia risk. Metformin is beneficial in treating conditions like polycystic ovary syndrome due to its insulin-resistance reduction capability. The drug's primary action involves curtailing hepatic gluconeogenesis, a significant contributor to high blood...
175
Oral Hypoglycemic Agents: α-Glucosidase Inhibitors01:19

Oral Hypoglycemic Agents: α-Glucosidase Inhibitors

α-glucosidase inhibitors, including acarbose (Precose), miglitol (Glyset), and voglibose (Voglib) (primarily available in Asia), are drugs that control blood sugar levels by delaying the digestion of starch and disaccharides. They achieve this by inhibiting α-glucosidase enzymes in the intestine, which slow the absorption of carbohydrates in the intestine, which in turn leads to a prolonged release of the glucoregulatory hormone GLP-1 from intestinal L-cells.
Acarbose and miglitol are...
160
GPCRs Regulate Adenylyl Cylase Activity01:09

GPCRs Regulate Adenylyl Cylase Activity

Some GPCRs transmit signals through adenylyl cyclase (AC), a transmembrane enzyme. AC helps synthesize second messenger cyclic adenosine monophosphate (cAMP). AC catalyzes cyclization reaction and converts ATP to cAMP by releasing a pyrophosphate. The pyrophosphate is further hydrolyzed to phosphate by the enzyme pyrophosphatase, which drives cAMP synthesis to completion. However, cAMP is rapidly degraded to 5′ AMP by the enzymes phosphodiesterase (PDE), preventing overstimulation of...
5.3K
Treatment for Pulmonary Arterial Hypertension: Prostacyclin Receptor Agonists01:23

Treatment for Pulmonary Arterial Hypertension: Prostacyclin Receptor Agonists

Prostacyclin receptor agonists are a class of therapeutic agents integral to managing pulmonary arterial hypertension (PAH). These drugs operate by mimicking the action of prostaglandin I2, or PGI2, a naturally occurring compound in the body.
These agonists bind to the IPR receptor situated on the plasma membrane of the pulmonary artery smooth muscle cells. This binding triggers a cascade of reactions known as the GS-AC-cAMP-PKA pathway. This pathway results in the relaxation of smooth muscle...
154