Searched over 200M research papers
5 papers analyzed
These studies suggest that metformin has potential benefits in certain conditions like PCOS and hormone receptor-positive breast cancer, but it may not be effective in chemoprevention or improving survival in non-diabetic metastatic breast cancer, and its mechanisms involve interactions with cellular components like caveolin1 and AMPK.
20 papers analyzed
Metformin is a widely used medication for managing type 2 diabetes. It works by reducing glucose production in the liver and improving insulin sensitivity. Metformin ER (Extended Release) is a formulation designed to release the drug slowly over time, potentially reducing gastrointestinal side effects and improving patient compliance.
Metformin has shown significant benefits in improving endometrial receptivity (ER) in women with polycystic ovary syndrome (PCOS). A meta-analysis of 62 studies involving 6571 patients demonstrated that metformin significantly increased endometrial thickness (EMT) and reduced endometrial artery resistance index (RI), which are critical factors for successful implantation and pregnancy. Additionally, metformin improved clinical pregnancy rates and reduced miscarriage rates in PCOS patients.
The role of metformin in breast cancer treatment has been explored in several studies with mixed results. A phase 3 randomized clinical trial (MA.32) involving 3649 patients with high-risk nonmetastatic breast cancer found that metformin did not significantly improve invasive disease-free survival compared to placebo. Similarly, another study on rodent models of mammary cancer (both ER+ and ER-) showed no preventive efficacy of metformin, and in some cases, it even increased tumor multiplicity. A phase II trial also reported no significant effect of metformin on progression-free survival, overall survival, or response rate in women with metastatic breast cancer receiving standard chemotherapy.
Metformin has been shown to alleviate high glucose-induced endoplasmic reticulum (ER) stress and inflammation in rat astrocytes by inhibiting the interaction between caveolin1 and AMPKα. This mechanism suggests potential therapeutic benefits of metformin in conditions characterized by hyperglycemia-induced ER stress and inflammation, such as neuropathological diseases.
While metformin has demonstrated clear benefits in improving endometrial receptivity in PCOS patients, its efficacy in breast cancer treatment remains inconclusive. The extended-release formulation, Metformin ER, may offer advantages in terms of patient compliance and reduced side effects, but further research is needed to fully understand its comparative benefits. Overall, metformin continues to be a valuable drug in the management of type 2 diabetes and other conditions, with ongoing research exploring its full potential.
Most relevant research papers on this topic