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Mapping the current research landscape of metformin in cancer based on bibliometric analysis
Yuan Wang1, Sike He1, Ziqi Li1
1Department of Urology, Institute of Urology, West China Hospital, Sichuan University, Chengdu, China.
Abstract:
Metformin, a widely prescribed first-line treatment for type 2 diabetes, has attracted significant attention for its potential anticancer effects. However, despite the rapid expansion of literature over the past two decades, research on the relationship between metformin and cancer remains highly fragmented, making it difficult to achieve a cohesive understanding of its mechanisms and therapeutic relevance across diverse cancer types. To address this gap, we integrated a bibliometric framework with bioinformatics analyses to systematically map the research landscape and uncover underlying molecular insights. Our findings reveal gene targets such as TP53, SIRT1, and HIF1A, key signaling pathways including AMPK/mTOR and p53, and cancer types like breast and colorectal cancer that are frequently associated with metformin, offering an integrative perspective to inform future cancer research.
Insights
Metformin shows potential anticancer effects, impacting genes like TP53 and pathways such as AMPK/mTOR. This research maps its relevance in breast and colorectal cancers, aiding future studies.
Area of Science:
- Oncology
- Pharmacology
- Bioinformatics
Background:
- Metformin is a primary treatment for type 2 diabetes.
- Growing evidence suggests metformin possesses anticancer properties.
- Existing research is fragmented, hindering a unified understanding of metformin's role in cancer.
Purpose of the Study:
- To systematically map the research landscape of metformin and cancer.
- To uncover molecular mechanisms and therapeutic relevance of metformin in diverse cancer types.
- To provide an integrated perspective for future cancer research.
Main Methods:
- Bibliometric analysis framework.
- Bioinformatics analyses.
- Systematic mapping of research literature.
Main Results:
- Identified key gene targets: TP53, SIRT1, and HIF1A.
- Highlighted significant signaling pathways: AMPK/mTOR and p53.
- Revealed frequent associations with breast and colorectal cancers.
Conclusions:
- Metformin's anticancer potential is supported by identified molecular targets and pathways.
- The study provides a cohesive overview of metformin's role across various cancers.
- Findings can guide future research into metformin-based cancer therapies.
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