Evidence map›Paper›PMID 40881348›Full record

ReviewFrontiers in cell and developmental biology2025

Protein lactylation in kidney diseases.

Yelei Xu, Xinming Li, Zhiguo Mao, Cheng Xue

Abstract readReview
In one paragraph

Review in Frontiers in cell and developmental biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Lactate Metabolism and Protein Lactylation in Diabetic Kidney Disease: A Narrative Review.Diabetes, metabolic syndrome and obesity : targets and therapy · 2026
    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

4 authors.

Yelei XuNaval Medical University (Second Military Medical University), Shanghai, China.
Xinming LiNaval Medical University (Second Military Medical University), Shanghai, China.
Zhiguo MaoDivision of Nephrology, Shanghai Changzheng Hospital, Second Affiliated Hospital of Naval Medical University (Second Military Medical University), Shanghai, China.
Cheng XueDivision of Nephrology, Shanghai Changzheng Hospital, Second Affiliated Hospital of Naval Medical University (Second Military Medical University), Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Post-translational modifications (PTMs) regulate protein function and structure through covalent modifications, participating in various physiological and pathological processes. Lysine lactylation is an emerging PTM discovered in recent years, which regulates gene expression, metabolism, and cell signaling by adding a lactyl group to lysine residues. As a by-product of glycolysis, lactate not only influences cellular metabolism but also contributes to the development and progression of kidney diseases through lactylation. This review focuses on the discovery and regulatory mechanisms of lysine lactylation, particularly its role in kidney diseases such as acute kidney injury, chronic kidney disease, and diabetic kidney disease. Lactylation influences the metabolic state, inflammatory response, and fibrosis of renal cells by modulating protein function and key gene transcription. With continued research, lactylation is expected to become a novel target for understanding the metabolic-epigenetic regulation of kidney diseases and could offer new strategies for treatment.

Indexed as

acute kidney injurychronic kidney diseasediabetic kidney diseaselactatelactylationpost-translational modification

Identifiers

PMID40881348
PMCPMC12380805

What OpenQuestion holds

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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.