Evidence map›Paper›PMID 42437897›Full record

SynthesisBMC cancer2026

Therapeutic effects of silibinin in preclinical animal models of gastrointestinal cancers: a systematic review and meta‑analysis.

Davood Mohammadi, Amir Hossein Aghayan, Diba Mohammadi, Zahra Jamalpoor

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in BMC cancer, 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

4 authors.

Davood MohammadiDepartment of Medical Genetics, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Amir Hossein AghayanStudents' Scientific Research Center, Tehran University of Medical Sciences, Tehran, Iran. amirhaghayan2022@gmail.com.
Diba MohammadiDepartment of Immunology, School of Medicine, Babol University of Medical Sciences, Babol, Iran.
Zahra JamalpoorTrauma and Surgery Research Center, Aja University of Medical Sciences, Tehran, Iran. z_jamalpoor2000@yahoo.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGastrointestinal (GI) cancers represent a leading cause of cancer-related mortality worldwide. Silibinin, the primary active constituent of milk thistle, possesses anti-proliferative, pro-apoptotic, and anti-inflammatory properties. This study systematically evaluates the therapeutic effects of silibinin in preclinical animal models of GI cancers.

methodsPubMed, Embase, Web of Science, and Scopus were searched following PRISMA 2020 guidelines. Studies were selected based on PICOS criteria, and risk of bias was assessed using the SYRCLE tool. Outcomes were pooled using a random-effects model and reported as standardized mean differences (SMDs) with 95% confidence intervals. Subgroup and sensitivity analyses were performed to address heterogeneity.

resultsFourteen studies met inclusion criteria. Silibinin significantly reduced tumor volume (SMD = -2.72) and tumor weight (SMD = -1.86), demonstrating promising antitumor efficacy. Notably, body weight was not significantly altered (SMD = 0.53, 95% CI: -0.41 to 1.48) and diet consumption showed a significant increase (SMD = 1.09), together indicating that silibinin exerts its anticancer effects without compromising nutritional status suggesting preliminary tolerability in animal models. At the molecular level, PCNA expression was significantly suppressed (SMD = -4.31), reflecting a consistent reduction in cellular proliferation, while apoptosis was significantly elevated (SMD = 6.00), confirming pro-apoptotic activity across GI cancer models.

conclusionSilibinin significantly suppresses tumor growth and promotes apoptosis in preclinical GI cancer models while demonstrating encouraging preliminary tolerability. These findings support its potential as an adjunctive anticancer agent; however, further clinical studies are warranted to validate these results and enable more definitive conclusions regarding its therapeutic efficacy.

Indexed as

Gastrointestinal NeoplasmsSilybinAnimalsApoptosisCell ProliferationDisease Models, AnimalTumor BurdenSilybinAntineoplastic AgentsGastrointestinal NeoplasmsMeta-AnalysisPreclinical StudiesSilibininTumor volume

Identifiers

PMID42437897
PMCPMC13644050

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.