Metformin: From Diabetes to Cancer-Unveiling Molecular Mechanisms and Therapeutic Strategies.
Emilia Amengual-CladeraPere Miquel Morla-BarceloAndrea Morán-CostoyaJorge Sastre-SerraDaniel Gabriel PonsAdamo VallePilar RocaMercedes Nadal-SerranoPublished in: Biology (2024)
Metformin, a widely used anti-diabetic drug, has garnered attention for its potential in cancer management, particularly in breast and colorectal cancer. It is established that metformin reduces mitochondrial respiration, but its specific molecular targets within mitochondria vary. Proposed mechanisms include inhibiting mitochondrial respiratory chain Complex I and/or Complex IV, and mitochondrial glycerophosphate dehydrogenase, among others. These actions lead to cellular energy deficits, redox state changes, and several molecular changes that reduce hyperglycemia in type 2 diabetic patients. Clinical evidence supports metformin's role in cancer prevention in type 2 diabetes mellitus patients. Moreover, in these patients with breast and colorectal cancer, metformin consumption leads to an improvement in survival outcomes and prognosis. The synergistic effects of metformin with chemotherapy and immunotherapy highlights its potential as an adjunctive therapy for breast and colorectal cancer. However, nuanced findings underscore the need for further research and stratification by molecular subtype, particularly for breast cancer. This comprehensive review integrates metformin-related findings from epidemiological, clinical, and preclinical studies in breast and colorectal cancer. Here, we discuss current research addressed to define metformin's bioavailability and efficacy, exploring novel metformin-based compounds and drug delivery systems, including derivatives targeting mitochondria, combination therapies, and novel nanoformulations, showing enhanced anticancer effects.
Keyphrases
- papillary thyroid
- type diabetes
- oxidative stress
- cardiovascular disease
- cell death
- end stage renal disease
- traumatic brain injury
- squamous cell carcinoma
- ejection fraction
- squamous cell
- single molecule
- working memory
- adipose tissue
- young adults
- peritoneal dialysis
- drug induced
- electronic health record
- endoplasmic reticulum
- wound healing