Evidence map›Paper›PMID 42799458›Full record

ReviewDrug design, development and therapy2026

Curcumin in Fibrosis Treatment: A Review.

Ling Deng, Xiaoqin Liu, Haoyue Feng, Boxun Zhang, Rensong Yue

Abstract readReview
In one paragraph

Review in Drug design, development and therapy, 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

5 authors.

Ling Deng *Department of Endocrinology and Metabolism, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan, People's Republic of China.ORCID 0009-0004-1660-3823
Xiaoqin Liu *Department of Endocrinology and Metabolism, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan, People's Republic of China.
Haoyue FengDepartment of Endocrinology and Metabolism, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan, People's Republic of China.
Boxun ZhangDepartment of Endocrinology and Metabolism, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan, People's Republic of China.
Rensong YueDepartment of Endocrinology and Metabolism, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fibrosis, marked by excessive accumulation of extracellular matrix (ECM) components, ultimately leads to dysfunction and failure of multiple organs, yet effective therapeutic options remain scarce. Curcumin (CUR), a naturally occurring polyphenol with diverse biological activities, has emerged as a promising candidate for anti-fibrotic intervention. Its designation as Generally Recognized as Safe (GRAS) and widespread use as a food additive offer distinct advantages for its incorporation into functional foods or clinical formulations. Nevertheless, its therapeutic translation is significantly limited by poor aqueous solubility and low systemic bioavailability. In response, a range of advanced drug delivery platforms-such as liposomes, nanoparticles, solid dispersions, and self-microemulsifying drug delivery systems (SMEDDS)-have been developed, markedly improving the solubility, stability, and in vivo bioavailability of CUR. This narrative review systematically summarizes the mechanistic, pharmacokinetic, and safety profiles of CUR in preclinical models of hepatic fibrosis (HF), myocardial fibrosis (MF), pulmonary fibrosis (PF), and renal fibrosis (RF) over the past two decades, focusing on core cellular effectors and signaling pathways. We further highlight recent progress in formulation strategies that potentiate CUR's anti-fibrotic efficacy, as well as key translational challenges: the pathological divergence between preclinical animal and in-vitro cell models and human fibrotic lesions, plus regulatory barriers limiting clinical adoption. Notably, most available mechanistic observations are derived from short-term pre-clinical experiments, and cannot be directly extrapolated to human chronic fibrotic disease. Despite these hurdles, cumulative preclinical evidence validates CUR's therapeutic potential as a natural anti-fibrotic agent in experimental settings. Combined with continuous innovation in delivery technology, CUR shows great prospects for developing anti-fibrotic functional foods and clinical therapeutics, yet high-quality human clinical trials are still urgently needed to confirm its real-world efficacy.

Indexed as

CurcuminFibrosisLiver CirrhosisAnimalsDrug Delivery SystemsHumansCurcuminanti-inflammationcurcuminfibrosisnatural productpharmacological mechanism

Identifiers

PMID42799458
PMCPMC13614314

What Socratic 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 Socratic graph.