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Embelin: A multifaceted anticancer agent with translational potential in targeting tumor progression and metastasis. | LitMetric

AI Article Synopsis

  • Embelin is a natural compound from the Embelia plant, known for its use in traditional medicine and pharmacological effects due to its unique chemical structure.
  • Recent studies highlight Embelin's role as a small inhibitor of XIAP, showing promising anticancer properties through mechanisms like apoptosis, cell cycle arrest, and autophagy across various cancer types.
  • The review emphasizes Embelin's ability to influence various signaling pathways (NF-κB, PI3Kinase/AKT, STAT3) to inhibit cancer cell growth, suggesting its potential clinical applications based on a decade of scientific research.

Article Abstract

Embelin, a natural para-benzoquinone product, is derived from plants of the Embelia genus, particularly Burm.f. A staple in traditional medicinal formulations for centuries, Embelin's pharmacological actions are attributed to the hydroxyl benzoquinone present in its structure. Its therapeutic potential is bolstered by unique physical and chemical properties. Recently, Embelin, recognized as a non-peptidic, cell-permeable small inhibitor of the X-linked inhibitor of apoptosis protein (XIAP), has garnered significant attention for its anticancer activity. It demonstrates various anticancer mechanisms, such as apoptosis induction, cell cycle arrest, and autophagy, in different cancer types. Additionally, Embelin modulates several signal transduction pathways, including NF-κB, PI3Kinase/AKT, and STAT3, effectively inhibiting the proliferation of diverse cancer cell lines. This literature review illuminates the anticancer potential of Embelin, detailing its mechanisms of action and prospective clinical applications, based on relevant scientific literature from the past decade sourced from various electronic databases. See also the Graphical abstract(Fig. 1).

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10792175PMC
http://dx.doi.org/10.17179/excli2023-6590DOI Listing

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