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Marine-Derived Compound Targeting mTOR and FGFR-2: A Promising Strategy for Breast, Lung, and Colorectal Cancer
Vijay Murali Ravi Mythili1, Kumaran K1, Sayantani Chattopadhyay1
1Department of Genetic Engineering, Integrated Genetics and Molecular Oncology Group, College of Engineering and Technology, SRM Institute of Science and Technology, Kattankulathur, Chennai, Tamilnadu, 603203, India.
Marine-derived compounds show promise as cancer therapeutics. A specific compound effectively inhibited key cancer-related proteins mTOR and FGFR2 in docking simulations, highlighting their therapeutic potential.
Area of Science:
- Marine biotechnology
- Drug discovery
- Computational chemistry
Background:
- Marine environments are rich sources of bioactive compounds with medicinal properties.
- Pharmaceutical research increasingly focuses on marine-derived natural products.
Purpose of the Study:
- To investigate the anticancer potential of marine bioactive compounds.
- To identify marine compounds that inhibit cancer-specific target proteins.
Main Methods:
- Gas Chromatography-Mass Spectrometry (GC-MS) for compound identification.
- Molecular docking simulations against cancer-associated proteins (mTOR, FGFR2).
Main Results:
- 1,4:3,6:5,7-Tribenzal-beta-mannoheptitol demonstrated inhibitory activity against mTOR (PDB ID: 4JSV) and FGFR2 (PDB ID: 6V6Q).
- Docking simulations proved effective in identifying potential therapeutic agents.
Conclusions:
- Marine-derived compounds, like 1,4:3,6:5,7-Tribenzal-beta-mannoheptitol, show significant potential for cancer drug development.
- Further research into these compounds could lead to novel cancer therapeutics.
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