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Meroterpenoids From Ganoderma lucidum Mushrooms and Their Biological Roles in Insulin Resistance and Triple-Negative Breast Cancer.


ABSTRACT: Ganoderma fungi as popular raw materials of numerous functional foods have been extensively investigated. In this study, five pairs of meroterpenoid enantiomers beyond well-known triterpenoids and polysaccharides, dayaolingzhiols I-M (1-5), were characterized from Ganoderma lucidum. Their structures were identified using spectroscopic and computational methods. Structurally, compound 1 features a novel dioxabicyclo[2.2.2]octan-3-one motif in the side chain. Ethnoknowledge-derived biological evaluation found that (+)-5 could activate Akt and AMPK phosphorylation in insulin-stimulated C2C12 cells, and (+)-5 could activate glucose uptake dose dependently in C2C12 cells. Furthermore, we found that (+)-1 (+)-4, and (-)-4 could significantly inhibit cell migration of the MDA-MB-231 cell line, of which (+)-4 showed significant inhibitory effects against cell migration of the MDA-MB-231 cell line in a dose-dependent manner. These findings revealed the meroterpenoidal composition of G. lucidum and its roles in the prevention of chronic diseases such as diabetes mellitus and triple-negative breast cancer.

SUBMITTER: Zhang JJ 

PROVIDER: S-EPMC8595597 | biostudies-literature | 2021

REPOSITORIES: biostudies-literature

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Meroterpenoids From <i>Ganoderma lucidum</i> Mushrooms and Their Biological Roles in Insulin Resistance and Triple-Negative Breast Cancer.

Zhang Jiao-Jiao JJ   Wang Dai-Wei DW   Cai Dan D   Lu Qing Q   Cheng Yong-Xian YX  

Frontiers in chemistry 20211103


<i>Ganoderma</i> fungi as popular raw materials of numerous functional foods have been extensively investigated. In this study, five pairs of meroterpenoid enantiomers beyond well-known triterpenoids and polysaccharides, dayaolingzhiols I-M (<b>1</b>-<b>5</b>), were characterized from <i>Ganoderma lucidum.</i> Their structures were identified using spectroscopic and computational methods. Structurally, compound <b>1</b> features a novel dioxabicyclo[2.2.2]octan-3-one motif in the side chain. Eth  ...[more]

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