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Published on: July 25, 2011
Quercetin as a multi-targeted therapeutic candidate in oral cancers: molecular mechanisms and preclinical evidence
Qamar Abuhassan1, Omer Qutaiba B Allela2, Wadhah Hasan Alkhazali3
1Department of Pharmaceutics and Pharmaceutical Technology, School of Pharmacy, University of Jordan, Amman, 11942, Jordan.
Abstract:
Oral malignancies, particularly oral squamous cell carcinoma (OSCC), are among the most prevalent head and neck cancers and remain associated with high morbidity, therapeutic resistance, and frequent recurrence. Despite multimodal treatment approaches, long-term survival remains suboptimal, highlighting the need for novel adjunctive strategies. Quercetin, a naturally occurring dietary flavonoid abundant in fruits and vegetables, has attracted attention due to its antioxidant, anti-inflammatory, and anticancer properties, with growing evidence supporting its relevance in oral cancer. In vitro studies demonstrate that quercetin significantly reduces oral cancer cell viability, proliferation, and clonogenic potential in a dose- and time-dependent manner. These effects are mediated by modulation of key cell-cycle regulators, resulting in arrest at the G1 and G2/M phases. Quercetin also promotes apoptosis through increased intracellular reactive oxygen species (ROS) generation, mitochondrial membrane depolarization, cytochrome c release, and activation of caspase-9 and caspase-3, indicating involvement of the intrinsic pathway. Concurrent activation of Fas/Fas-L signaling and caspase-8 suggests engagement of the extrinsic apoptotic pathway as well. Beyond cytotoxicity, quercetin suppresses migration and invasion by inhibiting epithelial-mesenchymal transition (EMT), characterized by increased E-cadherin and reduced N-cadherin and vimentin expression. It also downregulates MMP-2, MMP-9, and VEGF, thereby limiting extracellular matrix degradation and angiogenesis. In vivo studies further confirm reductions in tumor volume and growth kinetics without significant systemic toxicity. Nonetheless, although these findings underscore quercetin's multi-targeted anticancer potential, clinical translation is limited by poor bioavailability and rapid metabolism. Optimized delivery systems and well-designed clinical trials are necessary to clarify its therapeutic applicability in oral malignancies. This review will summarize current evidence on quercetin's anticancer effects in oral malignancies and highlight the molecular mechanisms underlying its therapeutic potential.
Insights
Quercetin, a natural flavonoid, shows significant anticancer effects against oral squamous cell carcinoma (OSCC) by inducing apoptosis and inhibiting cancer cell growth and spread. Further research is needed to overcome its poor bioavailability for clinical use.
Area of Science:
- Oncology
- Natural Products Chemistry
- Molecular Biology
Background:
- Oral squamous cell carcinoma (OSCC) presents significant challenges in treatment, with high recurrence rates and suboptimal survival.
- Novel therapeutic strategies are crucial to improve outcomes for patients with oral malignancies.
- Quercetin, a dietary flavonoid, exhibits promising antioxidant, anti-inflammatory, and anticancer properties relevant to oral cancer.
Purpose of the Study:
- To review the current evidence on quercetin's anticancer effects in oral malignancies.
- To elucidate the molecular mechanisms underlying quercetin's therapeutic potential against oral cancer.
- To highlight challenges and future directions for clinical translation of quercetin.
Main Methods:
- In vitro studies assessing quercetin's effects on oral cancer cell viability, proliferation, and apoptosis.
- Analysis of cell-cycle regulation, intrinsic and extrinsic apoptotic pathways, and epithelial-mesenchymal transition (EMT) markers.
- In vivo studies evaluating tumor growth and systemic toxicity.
Main Results:
- Quercetin significantly reduced oral cancer cell viability, proliferation, and clonogenic potential.
- Apoptosis was induced via both intrinsic (ROS, mitochondria, caspases) and extrinsic (Fas/Fas-L, caspase-8) pathways.
- Quercetin inhibited migration, invasion, EMT, angiogenesis (VEGF), and matrix degradation (MMP-2, MMP-9).
- In vivo studies showed reduced tumor volume and growth without significant toxicity.
Conclusions:
- Quercetin demonstrates multi-targeted anticancer potential against oral malignancies through various molecular mechanisms.
- Its efficacy in vitro and in vivo suggests therapeutic promise for oral cancer.
- Poor bioavailability and rapid metabolism are key limitations for clinical application, necessitating optimized delivery systems and clinical trials.
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