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Review Article

Critical Reviews on Anti-Cancer Effects of Edible and Medicinal Mushroom Phellinus linteus and Its Molecular Mechanisms

, , & ORCID Icon
Pages 1118-1137 | Published online: 13 May 2023
 

ABSTRACT

Phellinus linteus is a valuable edible and medicinal mushroom. Since the early 1990s, it has drawn significant attention from consumers due to its potential functional and medicinal benefits. P. linteus and its bioactive compounds have demonstrated various biological activities, such as antioxidant, anti-inflammatory, anticancer, and hepatoprotective agents. This review systematically summarized the anticancer effects of the edible and medicinal mushroom, P. linteus, and its molecular mechanisms. These findings are obtained from the databases of Web of Science, Google Scholar, PubMed, Scopus, and ResearchGate. Anticancer activities and their underlying mechanisms were mainly based on cancer cell proliferation inhibition, cell cycle arrest and apoptosis regulation, cell metastasis suppression, and immune cell activation. These effects are attributed to its bioactive components, viz. atractylenolide I, hispolon, and hispidin present in the mycelium and fruiting body. Based on our findings from the available literature, it is concluded that further comprehensive studies are required to identify all the bioactive compounds and the relationship between their structure and anticancer properties. Further, it is necessary to analyze its clinical use, safety, and efficacy alone as well as in combination with anticancer drugs.

Disclosure statement

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Abbreviation

AKT=

Protein kinase B

CDC2=

Cyclin-dependent kinase 2

CDK2=

cyclin-dependent kinase 2

CDK4=

cyclin-dependent kinase 4

CXCR4=

C-X-C motif chemokine receptor 4

EGFR=

epidermal growth factor receptor

EMT=

epithelial-mesenchymal transition

FAK,=

focal adhesion kinase

IFN-γ=

interferon gamma

IL-12=

interleukin 12

KRAS=

v-ki-ras2 Kirsten rat sarcoma viral oncogene homolog

LDH=

lactate dehydrogenase

MAPK=

mitogen-activated protein kinase

MMP-2=

matrix metalloproteinase-2

MMP-9=

matrix metalloproteinase-9

MTT=

3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2 H-tetrazolium bromide

MyD88=

myeloid differential factor

NK cells=

natural killer cells

Nrf2=

nuclear factor erythroid 2–related factor 2

PARP=

poly (ADP-ribose) polymerase;

PGE2=

prostaglandin E2

PI3K=

phosphoinositide 3-kinases;

SCID=

severe combined immunodeficiency

TCF/LEF=

T-cell factor/lymphoid enhancer factor

TNF-α=

tumor necrosis factor-alpha

VCAM1=

vascular cell adhesion molecule 1

VEGF=

Vascular endothelial growth factor

Additional information

Funding

This study is supported by a research grant 202107 from BNU-HKBU United International College

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