Evidence map›Paper›PMID 40500471›Full record

ReviewMedical oncology (Northwood, London, England)2025

Procyanidins as potential anticancer agents: mechanisms of action, bioavailability challenges and therapeutic opportunities.

Adedayo O Ademiluyi, Olubukola H Oyeniran, María Luisa Del Prado-Audelo, Alejandra Romero-Montero, Gerardo Leyva-Gómez, Irene Dini, Solomon Habtemariam, William N Setzer, Javad Sharifi-Rad, Daniela Calina

Abstract readReview
PubMed Publisher
In one paragraph

Review in Medical oncology (Northwood, London, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Fractionation-Based Modeling of Hawthorn (Molecules (Basel, Switzerland) · 2026
    Article
  2. Localization and Biological Activities of Bioflavonoids fromInternational journal of molecular sciences · 2026
    Article
  3. Review
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

10 authors.

Adedayo O AdemiluyiFunctional Foods and Nutraceuticals Unit, Department of Biochemistry, Federal University of Technology, Akure, 340252, Nigeria.
Olubukola H OyeniranDepartment of Biochemistry, Federal University, Oye-Ekiti, Nigeria.
María Luisa Del Prado-AudeloTecnologico de Monterrey, Campus Ciudad de México, 14380, Mexico City, Mexico.
Alejandra Romero-MonteroDepartamento de Farmacia, Facultad de Química, Universidad Nacional Autónoma de México, 04510, Mexico City, Mexico.
Gerardo Leyva-GómezDepartamento de Farmacia, Facultad de Química, Universidad Nacional Autónoma de México, 04510, Mexico City, Mexico. leyva@quimica.unam.mx.
Irene DiniDepartment of Pharmacy, University of Naples Federico II, Via Domenico Montesano 49, 80131, Naples, Italy. irdini@unina.it.
Solomon HabtemariamPharmacognosy Research & Herbal Analysis Services UK, Central Avenue, Chatham-Maritime, KEN, ME4 4TB, UK.
William N SetzerAromatic Plant Research Center, 230 N 1200 E, Suite 100, Lehi, UT, 84043, USA.
Javad Sharifi-RadUniversidad Espíritu Santo, Samborondón, 092301, Ecuador. javad.sharifirad@gmail.com.
Daniela CalinaDepartment of Clinical Pharmacy, University of Medicine and Pharmacy of Craiova, 200349, Craiova, Romania. calinadaniela@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Procyanidins (PCs), dietary polyphenols found in fruits, vegetables, and beverages, exhibit potent anticancer properties. Their mechanisms of action involve modulating oxidative stress, inhibiting angiogenesis, inducing apoptosis, and preventing tumor progression. Despite promising preclinical and clinical findings, their therapeutic potential remains underexplored. This review aims to provide a comprehensive analysis of the anticancer properties of PCs, including their bioavailability, pharmacokinetics, and safety. A systematic literature search was conducted across databases such as PubMed, Scopus, and Web of Science, utilizing Medical Subject Headings (MeSH) terms and specific keywords. Studies were selected based on predefined inclusion criteria, focusing on in vitro, in vivo, and clinical evidence. PCs demonstrate anticancer effects through multiple pathways, including inhibition of pro-inflammatory cytokines, suppression of the phosphoinositide 3-kinase/protein kinase B/mammalian target of rapamycin (PI3K/AKT/mTOR) and mitogen-activated protein kinase/extracellular signal-regulated kinase (MAPK/ERK) pathways, and regulation of apoptosis-related proteins such as BCL2-associated X protein (BAX), B-cell lymphoma 2 (BCL-2), and caspases. PCs demonstrate anticancer effects through multiple pathways, including inhibition of pro-inflammatory cytokines, suppression of the PI3K/AKT/mTOR and MAPK/ERK pathways, and regulation of apoptosis-related proteins such as BAX, BCL-2, and caspases. However, their low oral bioavailability and metabolic instability pose challenges for clinical application. Current research highlights the need for novel delivery systems, such as nanoparticles and liposomes, to enhance systemic absorption and therapeutic efficacy. Ongoing clinical trials are investigating the potential of PCs as adjuvants in cancer therapy, either alone or in combination with chemotherapeutic agents. Future studies should focus on optimizing their pharmacokinetics, exploring synergistic effects with existing treatments, and conducting large-scale clinical trials to validate their efficacy and safety. PCs hold promise as natural anticancer agents, with the potential to complement conventional therapies and improve patient outcomes.

Indexed as

Antineoplastic AgentsNeoplasmsProanthocyanidinsAnimalsApoptosisBiological AvailabilityHumansAntineoplastic AgentsProanthocyanidinsAntioxidantsBioavailabilityCancer preventionDrug resistanceFlavonoidsMetastasis inhibition

Identifiers

PMID40500471

What OpenQuestion holds

Textmetadata
Read underepoch 390

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 OpenQuestion graph.