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Isorhamnetin: Reviewing Recent Developments in Anticancer Mechanisms and Nanoformulation-Driven Delivery
Juie Nahushkumar Rana1, Kainat Gul2, Sohail Mumtaz3
1Fels Cancer Institute for Personalized Medicine, Lewis Katz School of Medicine at Temple University, Philadelphia, PA 19140, USA.
International Journal of Molecular Sciences
|August 14, 2025
Summary
Isorhamnetin, a natural flavonoid, shows significant anticancer potential by targeting key cancer mechanisms like cell cycle, apoptosis, and metastasis. This review highlights its promise as a safe and effective adjunct therapy in oncology.
Area of Science:
- Natural product chemistry
- Pharmacology
- Oncology
Background:
- Flavonoids, including isorhamnetin, are natural compounds with demonstrated anticancer activities and low toxicity.
- Isorhamnetin targets multiple cancer hallmarks, making it a compound of significant research interest.
Purpose of the Study:
- To comprehensively review the anticancer mechanisms of isorhamnetin.
- To explore recent advancements in isorhamnetin research, including nanoformulations and combination therapies.
Main Methods:
- Literature review of recent studies (2022-2024) on isorhamnetin's anticancer effects.
- Analysis of isorhamnetin's impact on cell cycle regulation, apoptosis, metastasis, angiogenesis, oxidative stress, and inflammation.
Main Results:
- Isorhamnetin inhibits cancer cell proliferation and induces apoptosis through caspase activation and mitochondrial dysfunction.
- It suppresses metastasis by downregulating matrix metalloproteinases (MMPs), vascular endothelial growth factor (VEGF), and epithelial-mesenchymal transition (EMT) markers.
- Isorhamnetin possesses antioxidant and anti-inflammatory properties, modulating the tumor microenvironment and potentially overcoming multidrug resistance.
Conclusions:
- Isorhamnetin is a versatile anticancer agent with potential as an adjunct therapy in oncology.
- Nanoformulation strategies enhance its delivery and bioavailability, improving therapeutic outcomes.
- Further research into combination therapies and specific signaling pathways is warranted.
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