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Updated: Jun 6, 2025

Polymalic Acid-based Nano Biopolymers for Targeting of Multiple Tumor Markers: An Opportunity for Personalized Medicine?
Published on: June 13, 2014
Synthesis and multifaceted evaluation of novel AgCZ nanocomposite for targeted anti-angiogenic cancer therapy
Yasser Hussein Issa Mohammed1, Ahmed Hassen Shntaif2, Ahd A Mansour3
1Department of Pharmacy, College of Medicine and Health Science , Hajjah University, Hajjah, Yemen. issayasser16@gmail.com.
Abstract:
Angiogenesis is the formation of blood vessels from the existing vasculature, which is important in the tumor growth where the metastatic spread, of cancer cells depends on an adequate supply of oxygen and nutrients and the removal of waste products. Targeting angiogenesis has emerged as a promising therapeutic strategy for cancer treatment. This study presents the synthesis and evaluation of a novel Ag-CeO2-ZnO (AgCZ) nanocomposite designed to specifically inhibit angiogenesis for effective cancer therapy. The nanocomposite was synthesized via a glycine-assisted combustion method, and its physicochemical properties were meticulously characterized using advanced analytical techniques. The anti-angiogenesis potential of the AgCZ nanocomposite was vigorously explored through an assortment of in vitro investigations, with a particular interest in inhibiting agents like vascular endothelial growth factor (VEGF). In silico data from molecular docking studies were instrumental in elucidating the nanocomposite's primary reported mechanism of action, i.e., its strong VEGF target bond. Notably, the nanocomposite had selective cytotoxicity with different types of cancer cells and no sign of serious influence onto normal cells, reflecting great promise of the targeted cancer therapy. Not and importantly, nanocomposite was implemented in vitro studies to measure its anti-angiogenic as well as anti-tumor effect in biological models additionally. Our study highlights emerging developments in medicine and draws possible future paths. The use of AgCZ composite nanoparticle is one of the potential anticancer drug and alternative to the conventional medicine which appears to be safer and more effectual, but further research is needed to overcome current limitations in clinical translation.
Insights
A novel silver-cerium oxide-zinc oxide (Ag-CeO2-ZnO) nanocomposite effectively inhibits angiogenesis, a key process in tumor growth. This promising anticancer agent shows selective toxicity to cancer cells, offering a potentially safer therapeutic alternative.
Area of Science:
- Nanotechnology
- Biomedical Engineering
- Oncology
Background:
- Angiogenesis, the formation of new blood vessels, is crucial for tumor growth and metastasis.
- Targeting angiogenesis is a key strategy in cancer therapy.
- Existing therapies face challenges, necessitating novel approaches.
Purpose of the Study:
- To synthesize and evaluate a novel Ag-CeO2-ZnO (AgCZ) nanocomposite for anti-angiogenesis and cancer therapy.
- To investigate the mechanism of action of the AgCZ nanocomposite.
- To assess the selective cytotoxicity of the AgCZ nanocomposite against cancer cells.
Main Methods:
- Glycine-assisted combustion synthesis of AgCZ nanocomposite.
- Physicochemical characterization using advanced analytical techniques.
- In vitro anti-angiogenesis assays, including inhibition of vascular endothelial growth factor (VEGF).
- In silico molecular docking studies.
- In vitro cytotoxicity assays on cancer and normal cells.
- In vitro anti-tumor and anti-angiogenic effect evaluation in biological models.
Main Results:
- The AgCZ nanocomposite was successfully synthesized and characterized.
- Molecular docking revealed strong binding affinity to VEGF, suggesting a mechanism of action.
- The nanocomposite exhibited selective cytotoxicity towards various cancer cell lines with minimal impact on normal cells.
- Demonstrated significant anti-angiogenic and anti-tumor effects in in vitro biological models.
Conclusions:
- The AgCZ nanocomposite shows significant potential as a targeted cancer therapeutic agent by inhibiting angiogenesis.
- Its selective cytotoxicity and mechanism targeting VEGF offer a promising alternative to conventional cancer treatments.
- Further research is warranted for clinical translation and overcoming current limitations.
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