Therapeutic Potential of Emodin for Gastrointestinal Cancers

Sierra J. McDonald(University of South Carolina), Brandon N. VanderVeen(University of South Carolina), Kandy T. Velázquez(University of South Carolina), Reilly T. Enos(University of South Carolina), Ciaran M. Fairman(University of South Carolina), Thomas D. Cardaci(University of South Carolina), Daping Fan(University of South Carolina), E. Angela Murphy(University of South Carolina)
Integrative Cancer Therapies
January 1, 2022
Cited by 32Open Access
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Abstract

Gastrointestinal (GI) cancers cause one-third of all cancer-related deaths worldwide. Natural compounds are emerging as alternative or adjuvant cancer therapies given their distinct advantage of manipulating multiple pathways to both suppress tumor growth and alleviate cancer comorbidities; however, concerns regarding efficacy, bioavailability, and safety are barriers to their development for clinical use. Emodin (1,3,8-trihydroxy-6-methylanthraquinone), a Chinese herb-derived anthraquinone, has been shown to exert anti-tumor effects in colon, liver, and pancreatic cancers. While the mechanisms underlying emodin's tumoricidal effects continue to be unearthed, recent evidence highlights a role for mitochondrial mediated apoptosis, modulated stress and inflammatory signaling pathways, and blunted angiogenesis. The goals of this review are to (1) highlight emodin's anti-cancer properties within GI cancers, (2) discuss the known anti-cancer mechanisms of action of emodin, (3) address emodin's potential as a treatment complementary to standard chemotherapeutics, (4) assess the efficacy and bioavailability of emodin derivatives as they relate to cancer, and (5) evaluate the safety of emodin.


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