Antitumor Activity and Mechanism of Terpenoids in Seaweeds Based on Literature Review and Network Pharmacology

被引:1
作者
Chen, Baoguo [1 ]
Li, Yaxin [1 ]
Li, Wei [2 ]
Ye, Shuhong [1 ]
Zhu, Lin [1 ]
Ding, Yan [1 ]
机构
[1] Dalian Polytech Univ, Natl Engn Res Ctr Seafood, Sch Food Sci & Technol, SKL Marine Food Proc & Safety Control, Dalian 116034, Liaoning, Peoples R China
[2] Korea Inst Oriental Med, Korean Med KM Applicat Ctr, Daegu 41062, South Korea
来源
ADVANCED BIOLOGY | 2024年 / 8卷 / 03期
基金
中国国家自然科学基金;
关键词
molecular docking; network pharmacology; seaweed; terpenoid; tumor; CYTOTOXIC HYDROAZULENE DITERPENES; HALOGENATED MONOTERPENES; NATURAL-PRODUCTS; BREAST-CANCER; MOLECULAR DOCKING; ALGA; PATHWAY; AKT; MERODITERPENOIDS; TRITERPENOIDS;
D O I
10.1002/adbi.202300541
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Seaweeds are a treasure trove of natural secondary metabolites. Terpenoids extracted from seaweeds are shown to possess a variety of antitumor cellular activities. However, due to the complex and diverse structures of terpenoids, their therapeutic targets and complex mechanisms of action have not been clarified. The present study summarises the research on terpenoids from seaweeds in oncological diseases over the last 20 years. Terpenoids show different degrees of inhibitory effects on different types of tumor cells, suggesting that terpenoids in seaweeds may have potential antitumor disease potential. Terpenoids with potential antitumor activity and their mechanism of action are investigated using network pharmacology. A total of 125 terpenoids and 286 targets are obtained. Proto-oncogene tyrosine-protein kinase Src(SRC), Signal transducer and activator of transcription 3 (STAT3), Mitogen-activated protein kinase (MAPK3, MAPK1), Heat shock protein HSP 90-alpha (HSP90AA1), Phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha (PIK3CA), and RAC-alpha serine/threonine-protein kinase (AKT1) are defined as core targets. According to GO function and Kyoto encyclopedia of genes and genomes(KEGG) enrichment analysis, terpenoids may affect the Phoshatidylinositol 3'-kinase (PI3K)-Akt signaling pathway, Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor resistance, Prostate cancer, MAPK signaling pathway, and Proteoglycans in cancer. In addition, the molecular docking results show that the selected terpenoids are all able to bind strongly to the active protein. Terpenoids may slow down the progression of cancer by controlling apoptosis, proliferation, and protein and enzyme binding. The present study summarises the research on terpenoids from seaweeds in oncological diseases over the last 20 years. Terpenoids with potential antitumor activity and their mechanism of action are investigated using network pharmacology and molecular docking approach. Terpenoids may slow down the progression of cancer by controlling apoptosis, proliferation, and protein and enzyme binding.image
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页数:15
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