Evidence map›Paper›PMID 40018013›Full record

ReviewFood science & nutrition2025

Exploring Punicalagin Potential Against Cancers: A Comprehensive Review.

Muhammad Hammad Ul Hassan, Muhammad Shahbaz, Ushna Momal, Hammad Naeem, Muhammad Imran, Mohamed A Abdelgawad, Mohammed M Ghoneim, Ehab M Mostafa, Ahmed H El-Ghorab, Suliman A Alsagaby and 3 more

Abstract readReview
In one paragraph

Review in Food science & nutrition, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
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  8. 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

13 authors.

Muhammad Hammad Ul HassanDepartment of Food Science and Technology Muhammad Nawaz Shareef University of Agriculture Multan Multan Pakistan.
Muhammad ShahbazDepartment of Food Science and Technology Muhammad Nawaz Shareef University of Agriculture Multan Multan Pakistan.
Ushna MomalDepartment of Food Science and Technology Muhammad Nawaz Shareef University of Agriculture Multan Multan Pakistan.
Hammad NaeemDepartment of Food Science and Technology Muhammad Nawaz Shareef University of Agriculture Multan Multan Pakistan.
Muhammad ImranDepartment of Food Science and Technology University of Narowal Pakistan.
Mohamed A AbdelgawadDepartment of Pharmaceutical Chemistry College of Pharmacy, Jouf University Sakaka Aljouf Saudi Arabia.
Mohammed M GhoneimDepartment of Pharmacy Practice College of Pharmacy, AlMaarefa University Riyadh Saudi Arabia.
Ehab M MostafaDepartment of Pharmacognosy College of Pharmacy, Jouf University Saudi Arabia.
Ahmed H El-GhorabDepartment of Chemistry College of Science, Jouf University Saudi Arabia.
Suliman A AlsagabyDepartment of Medical Laboratory Sciences College of Applied Medical Sciences, Majmaah University Saudi Arabia.
Waleed Al AbdulmonemDepartment of Pathology College of Medicine, Qassim University Buraidah Kingdom of Saudi Arabia.
Muzzamal HussainDepartment of Food Sciences Government College University Faisalabad Faisalabad Pakistan.
Tadesse Fenta YehualaFaculty of Chemical and Food Engineering, Bahir Dar Institute of Technology, Bahir Dar University Ethiopia.ORCID https://orcid.org/0000-0001-9241-0266

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Punicalagin, being a bioactive polyphenol, has gained significant interest owing to its potential anticancer effects. Researchers are studying punicalagin to determine its ability to inhibit cancer cell proliferation. This paper focuses on highlighting the therapeutic potential of punicalagin against tumors and cancers. Punicalagin inhibits tumor growth within the body through various cellular pathway interactions. This compound effectively eliminates tumor cells from the liver, stomach, prostate, and lungs. Different animal model studies have demonstrated the potential of punicalagin in blocking the MAPK/ERK and PI3K/AKT/mTOR signaling pathways, fighting against cancer. Through the inhibition of cell division, punicalagin may be capable of eradicating breast cancer cells. Punicalagin strongly inhibits the activities of vascular endothelial growth factor (VEGF), matrix metalloproteinase-9 (MMP-9), and uPA. Punicalagin effectively inhibits the androgen receptor (AR), a protein essential for the development and metastasis of prostate cancer. Lung cancer cells can be eliminated by initiating the caspase cascade and inhibiting protein synthesis, which is facilitated by punicalagin. In numerous animal models, punicalagin significantly reduces metastasis. Cyclokinase B1 and cyclin-dependent kinase 2 promote colon cancer; when colon cancer cells reach the G2/M phase, punicalagin induces apoptosis by inhibiting the action of these proteins. Punicalagin inhibits tumor development and cancer propagation by inhibiting blood vessel proliferation. There is still a need for further clinical trials and studies to fully reveal punicalagin's potential as well as its safety; despite the fact that it may decrease the threat of increasing tumors and provide an alternative treatment for many cancers.

Indexed as

androgen receptoranticancerantitumorcancerscell proliferationcolon cancerphytochemicalpunicalagin

Identifiers

PMID40018013
PMCPMC11866048

What OpenQuestion holds

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Registered trials

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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.