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Oleocanthal as a Multifunctional Anti-Cancer Agent: Mechanistic Insights, Advanced Delivery Strategies, and Synergies
Shirin Jannati1, Adiba Patel2, Rajashree Patnaik1
1Department of Basic Medical Sciences, College of Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai Health, Dubai P.O. Box 505055, United Arab Emirates.
Abstract:
Oleocanthal (OC), a secoiridoid phenolic compound exclusive to extra virgin olive oil (EVOO), has emerged as a promising nutraceutical with multifaceted anti-cancer properties. Despite its well-characterized anti-inflammatory and antioxidant effects, the mechanistic breadth and translational potential of OC in oncology remain underexplored and fragmented across the literature. This comprehensive review synthesizes and critically analyzes recent advances in the molecular, pharmacological, and translational landscape of OC's anti-cancer activities, providing an integrative framework to bridge preclinical evidence with future clinical application. We delineate the pleiotropic mechanisms by which OC modulates cancer hallmarks, including lysosomal membrane permeabilization (LMP)-mediated apoptosis, the inhibition of key oncogenic signaling pathways (c-MET/STAT3, PAR-2/TNF-α, COX-2/mPGES-1), the suppression of epithelial-to-mesenchymal transition (EMT), angiogenesis, and metabolic reprogramming. Furthermore, this review uniquely highlights the emerging role of OC in modulating drug resistance mechanisms by downregulating efflux transporters and sensitizing tumors to chemotherapy, targeted therapies, and immunotherapies. We also examine OC's bidirectional interaction with gut microbiota, underscoring its systemic immunometabolic effects. A major unmet need addressed by this review is the lack of consolidated knowledge regarding OC's pharmacokinetic limitations and drug-drug interaction potential in the context of polypharmacy in oncology. We provide an in-depth analysis of OC's poor bioavailability, extensive first-pass metabolism, and pharmacogenomic interactions, and systematically compile preclinical evidence on advanced delivery platforms-including nanocarriers, microneedle systems, and peptide-drug conjugates-designed to overcome these barriers. By critically evaluating the mechanistic, pharmacological, and translational dimensions of OC, this review advances the field beyond isolated mechanistic studies and offers a strategic blueprint for its integration into precision oncology. It also identifies key research gaps and outlines the future directions necessary to transition OC from a nutraceutical of dietary interest to a viable adjunctive therapeutic agent in cancer treatment.
Insights
Oleocanthal (OC), a compound from olive oil, shows broad anti-cancer effects by targeting multiple cancer pathways and overcoming drug resistance. Further research is needed to improve its delivery and clinical use in oncology.
Area of Science:
- Oncology
- Pharmacology
- Nutraceuticals
Background:
- Oleocanthal (OC), a secoiridoid from extra virgin olive oil (EVOO), exhibits promising anti-cancer properties.
- Existing research on OC's anti-cancer mechanisms and translational potential is fragmented.
- A comprehensive review is needed to synthesize OC's molecular, pharmacological, and translational oncology data.
Purpose of the Study:
- To comprehensively review and analyze OC's anti-cancer activities.
- To provide an integrative framework for OC's preclinical evidence and clinical application.
- To identify research gaps and future directions for OC in precision oncology.
Main Methods:
- Literature synthesis and critical analysis of recent advances in OC's anti-cancer research.
- Delineation of OC's mechanisms modulating cancer hallmarks (apoptosis, signaling pathways, EMT, angiogenesis, metabolism).
- Examination of OC's role in drug resistance, gut microbiota interactions, and pharmacokinetic limitations.
Main Results:
- OC modulates key cancer hallmarks via lysosomal membrane permeabilization (LMP)-mediated apoptosis and inhibition of oncogenic pathways.
- OC suppresses epithelial-to-mesenchymal transition (EMT), angiogenesis, and alters metabolic reprogramming.
- OC sensitizes tumors to therapies by downregulating efflux transporters and shows potential in overcoming drug resistance.
Conclusions:
- OC demonstrates pleiotropic anti-cancer effects and potential in overcoming drug resistance.
- Pharmacokinetic limitations (bioavailability, metabolism) and delivery strategies (nanocarriers) require further investigation.
- OC holds promise as an adjunctive therapeutic agent in precision oncology, necessitating further research for clinical translation.
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