Honokiol and its analogues as anticancer compounds: Current mechanistic insights and structure-activity relationship

dc.contributor.authorPrasher, Parteek
dc.contributor.authorFatima, Rabab
dc.contributor.authorSharma, Mousmee
dc.contributor.authorTynybekov, Bekzat
dc.contributor.authorAlshahrani, Asma M.
dc.contributor.authorAtessahin, Dilek Arslan
dc.contributor.authorCalina, Daniela
dc.date.accessioned2026-08-12T18:08:42Z
dc.date.issued2023
dc.departmentFırat Üniversitesi
dc.description.abstractLignans are plant-derived polyphenolic compounds with a plethora of biological applications. Also, regarded as phytoestrogens, the lignans offer a variety of health benefits of which the anti-cancer effects are the most attractive. Honokiol is a lignan isolated from various parts of trees belonging to the genus Magnolia. The bioactivity of honokiol is attributed to its characteristic physical properties, which include small size and the presence of two phenolic groups that may interact with proteins in cell membranes via hydrophobic interactions, aromatic pi orbital co-valency, and hydrogen bonding. The hydrophobicity of honokiol enables its rapid dissolution in lipids and the crossing of physiological barriers, including the blood-brain barrier and cerebrospinal fluid. These factors contribute towards the high bioavailability of honokiol which further support its candidature in medicinal research. Therefore, the anticancer properties of honokiol are of particular interest as many of the contemporary anticancer drugs suffer from bioavailability drawbacks, which necessitates the identification and development of novel candidate molecules directed as anticancer chemotherapeutics. The antioncogenic profile of honokiol also arises from the regulation of various signalling pathways associated with oncogenesis, arresting of the cell cycle by regulation of cyclic proteins, upregulation of epithelial markers and downregulation of mesenchymal markers leading to the inhibition of epithelial-mesenchymal transition, and preventing the metastasis by restricting cell migration and invasion due to the downregulation of matrix-metalloproteinases. In this review, we discuss the anticancer properties of honokiol.
dc.identifier.doi10.1016/j.cbi.2023.110747
dc.identifier.issn0009-2797
dc.identifier.issn1872-7786
dc.identifier.orcid0000-0002-2628-3622
dc.identifier.orcid0000-0002-7301-8151
dc.identifier.orcid0000-0002-1528-9367
dc.identifier.orcid0009-0003-6176-2113
dc.identifier.pmid37816447
dc.identifier.scopus2-s2.0-85173712635
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://doi.org/10.1016/j.cbi.2023.110747
dc.identifier.urihttps://hdl.handle.net/11508/63196
dc.identifier.volume386
dc.identifier.wosWOS:001094263600001
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherElsevier Ireland Ltd
dc.relation.ispartofChemico-Biological Interactions
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260511
dc.subjectHonokiol
dc.subjectCancer
dc.subjectSignalling pathways
dc.subjectMolecular mechanisms
dc.subjectStructure -anticancer activity relationship
dc.subjectApoptosis
dc.titleHonokiol and its analogues as anticancer compounds: Current mechanistic insights and structure-activity relationship
dc.typeReview Article

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