Exploring the anti-cancer properties of <i>Carissa carandas</i> as a multi-targeted approach against breast cancer
The escalating incidence of breast cancer globally presents a formidable challenge within oncology. Our research pursued an examination of the anti-cancer potential of <i>Carissa carandas</i>, a shrub traditionally used for medicinal purposes and known for its composition of vital nutrients and phytochemicals. We employed a network pharmacology strategy combined with molecular docking and molecular dynamics simulations to elucidate the intricate relationships between the phytochemical constituents of <i>C. carandas</i>, critical breast cancer proteins, and associated signaling pathways. The study highlighted a complex network of protein interactions, identifying AKT1, HIF1A, PTGS2, and GSK3B as key nodes within this network. These proteins are engaged by numerous investigated compounds from <i>C. carandas</i> and are fundamental in modulating crucial signaling pathways such as those involving Estrogen, HIF-1, Prolactin, VEGF, and Th17 cell differentiation-each of which plays a recognized role in breast cancer progression, affecting tumor growth, proliferation, and metastatic potential. Our analysis suggests that the phytochemicals in <i>C. carandas</i> may exert anti-cancer activity by synergistically modulating these pathways, highlighting the benefit of multi-targeted therapeutic approaches over single-targeted ones. In summary, through the application of advanced network pharmacology, molecular docking, MD simulations, and MM/PBSA analysis, our study offers a detailed exploration of the potential mechanisms by which <i>C. carandas</i> may exert anti-cancer effects. This sets a foundation for further in-depth experimental and clinical trials to validate these mechanisms and support the advancement of novel plant-derived therapeutic options towards breast cancer, with the possibility of significantly advancing the therapeutic options for this prevalent disease.
Authors
- Fahad Y. Sabei (ORCID: https://orcid.org/0000-0002-1412-5299)
- Khalid Zoghebi (ORCID: https://orcid.org/0000-0002-7401-5227)
- Awaji Y. Safhi (ORCID: https://orcid.org/0000-0002-2184-4339)
Institutions
- Pharmac (NZ)
- Jazan University (SA)
Publication Details
- Journal
- Journal of Biomolecular Structure and Dynamics
- Published
- 2024-12-11
- DOI
- https://doi.org/10.1080/07391102.2024.2437548
- Citations
- 1
- Primary Topic
- Computational Drug Discovery Methods
- Type
- article
- Field-Weighted Citation Impact
- 0.36