Metformin, initially prescribed as an oral hypoglycemic medication for type 2 diabetes, has recently gained attention for its potential anticancer effects. Its history dates to 1918, when guanidine, a component of the traditional European herb Galega officinalis, was found to reduce glycemia. This review precisely examines the mechanisms underlying Metformin's anticancer effects across various neoplastic conditions. This investigation explores the complex interactions between metformin and major signaling pathways associated with carcinogenesis, including AMP-activated protein kinase (AMPK), mTOR, and insulin-like growth factor (IGF) pathways. The review emphasizes Metformin's diverse effects on angiogenesis, inflammation, apoptosis, and cellular metabolism in cancer cells. Additionally, new data on metformin's capacity to alter the tumor microenvironment and enhance immune surveillance systems against cancer are examined. The review underscores Metformin's potential for repurposing in oncology, emphasizing its clinical relevance as an adjuvant therapy for various cancers. The review provides insightful information about the complex anticancer mechanisms of metformin by combining data from preclinical and clinical studies. These findings not only broaden our knowledge of the effects of metformin but also open new avenues for oncology research and treatment developments.
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http://dx.doi.org/10.1016/j.biochi.2025.03.002 | DOI Listing |
Biochimie
March 2025
Department of Medicine, Tulane University School of Medicine, New Orleans, LA 70112, USA. Electronic address:
Metformin, initially prescribed as an oral hypoglycemic medication for type 2 diabetes, has recently gained attention for its potential anticancer effects. Its history dates to 1918, when guanidine, a component of the traditional European herb Galega officinalis, was found to reduce glycemia. This review precisely examines the mechanisms underlying Metformin's anticancer effects across various neoplastic conditions.
View Article and Find Full Text PDFDiscov Oncol
March 2025
Department and Institute of Urology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, No.1095 Jiefang Avenue, 430030, Wuhan, People's Republic of China.
Introduction: An increasing number of studies have focused on the anti-tumor effect of metformin in recent years. However, the effect of metformin on different cancers remains controversial and lacks consensus.
Methods: A bidirectional two-sample Mendelian randomization (MR) design was used to assess causal relationships between metformin and 18 cancer types.
RSC Adv
February 2025
Department of Chemistry, Faculty of Science, The Maharaja Sayajirao University of Baroda Vadodara 390002 India
Monotherapy in diabetes management is losing interest due to its ineffectiveness in achieving optimal glycaemic control in a significant proportion of diabetic patients. Therefore, combined therapy is increasingly preferred by clinicians, which offers enhanced effectiveness and a better safety profile for managing the condition. The present work deals with the designing of a dual drug nanocarrier based on MCM-48 and 12-tungtophosphoric acid (TPA) for the co-delivery of Glipizide (GLP) and Metformin Hydrochloride (MTF) as well as its characterization using various techniques.
View Article and Find Full Text PDFAsian Pac J Cancer Prev
February 2025
Biotechnology Department, Faculty of Science, Cairo University, Giza, Egypt.
Background: Cancer has become the second cause of death worldwide after cardiovascular diseases. Thus, the development of efficient therapeutic approaches for cancer treatment seems necessary. One of the promising approaches is depending on nanotechnology in terms of drug delivery systems.
View Article and Find Full Text PDFJ Appl Oral Sci
February 2025
Jeonbuk National University, Institute of Oral Bioscience, School of Dentistry, Department of Oral Biochemistry, Jeonju, Korea.
Objective: This study evaluated whether hypoglycemic drug metformin enhances the anti-cancer effects of cisplatin in YD-9 cells.
Methodology: YD-9 cells, derived from oral mucosal squamous cell carcinoma of oral mucosa, were used to assess the combined effects of metformin and cisplatin by means of MTT assay, live and dead cell staining, and colony formation assays to evaluate cell viability and proliferation. Reactive oxygen species level was measured using a Muse cell analyzer.
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