AI Article Synopsis
- The investigation aimed to identify the active compounds in airpotato yam rhizome (AYR) and how they could potentially treat colorectal cancer (CRC).
- Using network pharmacology and molecular docking, researchers predicted that quercetin in AYR primarily targets EGFR and AKT1, crucial in the EGF/EGFR-induced PI3K/AKT pathway.
- In experiments, AYR showed the ability to inhibit the PI3K/AKT pathway, leading to increased cancer cell death in both cell cultures and mouse models, suggesting its promise as a CRC treatment.
Article Abstract
Objective: The objective of this investigation was to elucidate the key active compounds and molecular mechanisms underlying the therapeutic potential of airpotato yam rhizome (AYR) in colorectal cancer (CRC) treatment.
Methods: By utilizing network pharmacology and molecular docking, key targets and signaling pathways of AYR against CRC were predicted and subsequently validated in cellular and mouse xenograft models.
Results: This study initially predicted that quercetin was the primary compound in AYR that might have potential efficacy against CRC and that EGFR and AKT1 could be the main targets of AYR, with the EGF/EGFR-induced PI3K/AKT signaling pathway potentially playing a crucial role in the anti-CRC effects of AYR. Molecular docking analysis further indicated a strong binding affinity between quercetin and EGFR, primarily through hydrogen bonds. Additionally, the AYR-derived drug-containing serum was found to inhibit the PI3K/AKT signaling pathway, as demonstrated by decreased levels of p-PI3K, p-AKT, and BCL2, which ultimately led to enhanced apoptosis of HCT116 and HT29 cells. The potential antitumor effects of AYR were investigated in nude mouse xenograft models of human HCT116 and HT29 cells, in which AYR was found to induce tumor cell apoptosis and inhibit tumor formation.
Conclusion: AYR may promote CRC cell apoptosis by suppressing the PI3K/AKT signaling pathway, which provides a basis for further research on the safe and effective use of AYR for the treatment of CRC.
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|---|---|
| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11327141 | PMC |
| http://dx.doi.org/10.3389/fonc.2024.1414766 | DOI Listing |
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