Evidence map›Paper›PMID 41596631›Full record

ReviewInternational journal of molecular sciences2026

Regulation of Keratin Chemical Modifications: Potential Molecular Mechanisms in Proliferative Diseases.

Xuemei Ma, Xiaoli Jiang, Mengxue Song, Bingbing Bai, Xia Hou, Qingtian Wu

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 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

6 authors.

Xuemei MaDepartment of Basic Medicine, Jiamusi University, Jiamusi 154007, China.
Xiaoli JiangDepartment of Basic Medicine, Jiamusi University, Jiamusi 154007, China.
Mengxue SongDepartment of Clinical Medicine, Jiamusi University, Jiamusi 154007, China.
Bingbing BaiDepartment of Basic Medicine, Jiamusi University, Jiamusi 154007, China.
Xia HouDepartment of Basic Medicine, Jiamusi University, Jiamusi 154007, China.
Qingtian WuDepartment of Basic Medicine, Jiamusi University, Jiamusi 154007, China.

Funding

The team for the national key specialized project, the respiratory and critical care research team GJ202302
6 · The paper itself

Abstract

Keratin, a core structural protein in epithelial cells, is essential for maintaining epithelial tissue integrity. Numerous studies have confirmed its critical role in proliferative disorders, including lung/liver cancer, idiopathic pulmonary fibrosis (IPF), and hepatic fibrosis (HF). Post-translational modification (PTM) regulates protein activity, and keratin undergoes phosphorylation, acetylation, and methylation-modifications that modulate fibrosis and cancer progression by regulating relevant signaling pathways. However, how these modifications reshape keratin's structure and function in these diseases remains understudied, underscoring the necessity for a systematic review. This review first summarizes keratin's classification, physiological functions, and roles in epithelial cells, then focuses on the physiological significance of keratin modifications in fibrosis and cancer, while dissecting the molecular mechanisms by which keratin PTMs drive disease progression to address the knowledge gap regarding modification-related keratin changes. Elucidating the mechanisms of keratin and its PTMs is pivotal for understanding disease progression and developing targeted therapies; meanwhile, keratin-targeted strategies-such as keratin siRNAs and small-molecule compounds that regulate keratin expression or modification-have shown therapeutic potential. In summary, this review synthesizes current research findings and provides novel insights for the treatment of fibrosis and cancer.

Indexed as

KeratinsNeoplasmsProtein Processing, Post-TranslationalAnimalsEpithelial CellsHumansSignal TransductionKeratinsepithelial cellsfibrosis and cancerkeratinprotein modification

Identifiers

PMID41596631
PMCPMC12842078

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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.