Evidence map›Paper›PMID 42234050›Full record

ReviewMolecular biology reports2026

Quercetin as a multi-targeted therapeutic candidate in oral cancers: molecular mechanisms and preclinical evidence.

Qamar Abuhassan, Omer Qutaiba B Allela, Wadhah Hasan Alkhazali, Jalpa R Patel, K V Jamuna, Vandana Tripathi, Samir Sahoo, Neeraj Bainsal, Malika Akhrorova, Hayder Naji Sameer and 3 more

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In one paragraph

Review in Molecular biology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Qamar AbuhassanDepartment of Pharmaceutics and Pharmaceutical Technology, School of Pharmacy, University of Jordan, Amman, 11942, Jordan.
Omer Qutaiba B AllelaCollege of Pharmacy, Alnoor University, Mosul, Iraq. omerallela@alnoor.edu.iq.
Wadhah Hasan AlkhazaliAhl al bayt University, Kerbala, Iraq.
Jalpa R PatelDepartment of Pharmacy, Faculty of Pharmacy, Gokul Global University, Sidhpur, Gujarat, India.
K V JamunaDepartment of Forensic Science, School of Sciences, JAIN (Deemed to be University), Bangalore, Karnataka, India.
Vandana TripathiDepartment of Pharmacy, Sharda School of Pharmacy, Sharda University, Greater Noida, India.
Samir SahooDepartment of General Medicine, IMS and SUM Hospital, Siksha 'O' Anusandhan (Deemed to be University), Bhubaneswar, Odisha, India.
Neeraj BainsalUniversity Institute of Pharma Sciences, Chandigarh University, Mohali, Punjab, India.
Malika AkhrorovaDepartment of Pediatric Dentistry, Samarkand State Medical University, 18 Amir Temur Street, Samarkand, Uzbekistan.
Hayder Naji SameerCollage of Pharmacy, National University of Science and Technology, Dhi Qar, 64001, Iraq.
Ahmed YaseenGilgamesh Ahliya University, Baghdad, Iraq.
Zainab H AthabDepartment of Pharmacy, Al-Zahrawi University College, Karbala, Iraq.
Mohaned AdilPharmacy college, Al-Farahidi University, Baghdad, Iraq.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Carcinoma, Squamous CellMouth NeoplasmsQuercetinAnimalsAntineoplastic AgentsAntioxidantsApoptosisCell ProliferationEpithelial-Mesenchymal TransitionHumansReactive Oxygen SpeciesSignal TransductionAntineoplastic AgentsAntioxidantsQuercetinReactive Oxygen SpeciesApoptosisHead and Neck CancersMetastasisOral CancerOral Squamous Cell CarcinomaQuercetin

Identifiers

What Socratic holds

Textmetadata
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.