Combination of metabolomics and network pharmacology analysis to decipher the mechanisms of total flavonoids of Litchi seed against prostate cancer

Author:

Cui Dianxin12ORCID,Luo Zhuo1,Liu Xi3,Chen Xin12,Zhang Qiuping24,Yang Xin2,Lu Qinpei1,Su Zhiheng1ORCID,Guo Hongwei12ORCID

Affiliation:

1. Guangxi Key Laboratory of Bioactive Molecules Research and Evaluation & Guangxi Health Commission Key Laboratory of Basic Research on Anti-geriatric Drugs, Pharmaceutical college, Guangxi Medical University , Nanning 530021 , China

2. Key Laboratory of Longevity and Aging-related Diseases of Chinese Ministry of Education & Center for Translational Medicine, Guangxi Medical University , Nanning, 530021 , China

3. College of Chemistry and Chemical Engineering, Xiamen University , Xiamen 361005 , China

4. The First Affiliated Hospital of Guangxi Medical University , Nanning 530021 , China

Abstract

Abstract Objectives To explore the underlying mechanism of total flavonoids of Litchi seed (TFLS) in treating prostate cancer (PCa). Methods Cell Counting Kit-8 (CCK-8), EdU incorporation assay, trypan blue dye assay and colony formation assay were employed to evaluate the effect of TFLS on PCa in vitro. The xenograft mouse model was established to explore the anti-tumour effect of TFLS in vivo. Alterations in the metabolic profiles of the PC3 cells and mouse serum were obtained by untargeted metabolomics. Combination with metabolomics analysis and network pharmacology strategies, the potential targets were predicted and further validated by RT-qPCR. Key findings TFLS attenuated PCa progression both in vitro and in vivo. Metabolomics results yielded from cells and serum indicated that the anti-cancer effect of TFLS was correlated with synergistic modulation of five common metabolic pathways including glycerophospholipid metabolism, arginine and proline metabolism, glycine, serine and threonine metabolism, tryptophan metabolism and steroid biosynthesis. Using in silico prediction and RT-qPCR analysis, we further revealed that TFLS exerted anti-PCa activities via regulating the expressions of nine genes, including MAOA, ACHE, ALDH2, AMD1, ARG1, PLA2G10, PLA2G1B, FDFT1 and SQLE. Conclusions TFLS suppressed tumour proliferation in PCa, which may be associated with regulating lipid and amino acid metabolisms.

Funder

Guangxi key research and development project

National Natural Science Foundation of China

Guangxi Medical University

Publisher

Oxford University Press (OUP)

Subject

Pharmaceutical Science,Pharmacology

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