Evidence mapPaperPMID 40458228Full record

ReviewInternational journal of general medicine2025

The Dual Role and Therapeutic Implications of the Wnt/β-Catenin Pathway in Diabetic Kidney Disease.

Yilinuer Adeerjiang, Xiao-Xue Gan, Wen-Ting Li, Qin-Tian Li, Yi-Qi Jiang, Xia Zhu, Chen-Ming Hu, Pan-Xia Wang, Sheng Jiang

Abstract readReview
In one paragraph

Review in International journal of general medicine, 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. Review
  2. Review
  3. Review
  4. Article
  5. Multi-Omics Integration IdentifiesInternational journal of molecular sciences · 2025
    Article
  6. Review
  7. Article
  8. Article
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

9 authors.

Yilinuer AdeerjiangDepartment of Endocrinology, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, People's Republic of China.ORCID 0009-0003-9402-8601
Xiao-Xue GanDepartment of Endocrinology, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, People's Republic of China.
Wen-Ting LiFirst Clinical Medical College of Xinjiang Medical University, Urumqi, People's Republic of China.
Qin-Tian LiFirst Clinical Medical College of Xinjiang Medical University, Urumqi, People's Republic of China.
Yi-Qi JiangFirst Clinical Medical College of Xinjiang Medical University, Urumqi, People's Republic of China.
Xia ZhuFirst Clinical Medical College of Xinjiang Medical University, Urumqi, People's Republic of China.
Chen-Ming HuFirst Clinical Medical College of Xinjiang Medical University, Urumqi, People's Republic of China.ORCID 0009-0002-0632-7832
Pan-Xia WangDepartment of Endocrinology, People's Hospital of Kashgar, Kashgar, People's Republic of China.
Sheng JiangDepartment of Endocrinology, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diabetic kidney disease (DKD), a major microvascular complication of diabetes, affects 30-40% of patients and is the leading cause of end-stage renal disease. The Wnt/β-catenin signaling pathway plays a dual role in DKD pathogenesis: its moderate activation protects against hyperglycemia-induced mesangial apoptosis, while chronic overactivation exacerbates renal fibrosis, podocyte injury, and tubular dysfunction. This review synthesizes current evidence on the pathway's context-dependent mechanisms. Emerging therapeutic strategies-including small-molecule inhibitors (eg, Dickkopf-1), monoclonal antibodies, and natural compounds like curcumin and Salvia miltiorrhiza extracts-show preclinical promise in modulating Wnt/β-catenin activity. However, clinical translation faces challenges such as pathway redundancy, off-target effects, and the need for precise dosing to balance protective and injurious outcomes. Recent advances in biomarker discovery (eg, urinary β-catenin) and ongoing clinical trials highlight the pathway's potential as a therapeutic target. Future research must prioritize patient stratification, combination therapies (eg, Wnt inhibitors + RAAS blockers), and mechanistic studies to address unresolved controversies in Wnt signaling dynamics. This work underscores the therapeutic implications of targeting Wnt/β-catenin in DKD while advocating for a nuanced approach to harness its protective roles.

Indexed as

diabetic kidney diseasetherapyWnt/β-catenin pathway

Identifiers

PMID40458228
PMCPMC12127529

What Socratic holds

Textmetadata
LicenceCC BY-NC
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.