Xintongtai Granule: Investigating the serum pharmacology and mechanisms of action against atherosclerosis

Du, Lixin; Long, Hongping; Wei, Jiaming; Lu, Huiling; Xiao, Yifei; Li, Ya; Guo, Zhihua

doi:10.1016/j.jchromb.2024.124165

Journal of Chromatography B

2024

DOI: 10.1016/j.jchromb.2024.124165

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Xintongtai Granule: Investigating the serum pharmacology and mechanisms of action against atherosclerosis

Lixin Du,

Hongping Long,

Jiaming Wei

et al.

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2024

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Cited by 2 publications

References 35 publications

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Study on the Anti-Atherosclerotic Mechanisms of Xin-Tong-Tai Granule Through Network Pharmacology, Molecular Docking, and Experimental Validation

Zhu,

Wang,

Liu

et al. 2024

JIR

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Study on the Anti-Atherosclerotic Mechanisms of Xin-Tong-Tai Granule Through Network Pharmacology, Molecular Docking, and Experimental Validation

Zhu,

Wang,

Liu

et al. 2024

JIR

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Unveiling the therapeutic potential of airpotato yam rhizome against colorectal cancer: a network pharmacology approach

Xie,

Xu,

Chen

et al. 2024

Front. Oncol.

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ObjectiveThe 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.MethodsBy 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.ResultsThis 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.ConclusionAYR 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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Xintongtai Granule: Investigating the serum pharmacology and mechanisms of action against atherosclerosis

Cited by 2 publications

References 35 publications

Study on the Anti-Atherosclerotic Mechanisms of Xin-Tong-Tai Granule Through Network Pharmacology, Molecular Docking, and Experimental Validation

Study on the Anti-Atherosclerotic Mechanisms of Xin-Tong-Tai Granule Through Network Pharmacology, Molecular Docking, and Experimental Validation

Unveiling the therapeutic potential of airpotato yam rhizome against colorectal cancer: a network pharmacology approach

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