Evidence map›Paper›PMID 36157258›Full record

ArticleKidney diseases (Basel, Switzerland)2022

Treatment of Membranous Nephropathy by Disulfiram through Inhibition of Podocyte Pyroptosis.

Daoyuan Lv, Song Jiang, Mingchao Zhang, Xiaodong Zhu, Fan Yang, Hui Wang, Shen Li, Feng Liu, Caihong Zeng, Weisong Qin and 2 more

Abstract read
In one paragraph

Article in Kidney diseases (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
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  3. Review
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  5. Article
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  7. Review
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  11. Review
  12. Article
  13. Regulated cell death pathways in kidney disease.Nature reviews. Nephrology · 2023
    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

12 authors.

Daoyuan LvDepartment of Nephrology, Jinling Hospital, The First School of Clinical Medicine, Southern Medical University, Nanjing, China.
Song JiangNational Clinical Research Center of Kidney Diseases, Jinling Hospital, Nanjing, China.
Mingchao ZhangNational Clinical Research Center of Kidney Diseases, Jinling Hospital, Nanjing, China.
Xiaodong ZhuNational Clinical Research Center of Kidney Diseases, Jinling Hospital, Nanjing, China.
Fan YangNational Clinical Research Center of Kidney Diseases, Jinling Hospital, Nanjing, China.
Hui WangNational Clinical Research Center of Kidney Diseases, Jinling Hospital, Nanjing, China.
Shen LiNational Clinical Research Center of Kidney Diseases, Jinling Hospital, Nanjing, China.
Feng LiuNational Clinical Research Center of Kidney Diseases, Jinling Hospital, Nanjing, China.
Caihong ZengNational Clinical Research Center of Kidney Diseases, Jinling Hospital, Nanjing, China.
Weisong QinNational Clinical Research Center of Kidney Diseases, Jinling Hospital, Nanjing, China.
Limin LiSchool of Life Science and Technology, China Pharmaceutical University, Nanjing, China.
Zhihong LiuDepartment of Nephrology, Jinling Hospital, The First School of Clinical Medicine, Southern Medical University, Nanjing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Membranous nephropathy (MN) is a common chronic kidney disease in adults and a major challenge of clinical practice for its treatment. Despite major advances, since the discovery of the phospholipase A2 receptor as the major autoantigen of podocytes in MN, the mechanisms leading to glomerular damage remain elusive. Pyroptosis, a newly discovered type of programed necrotic cell death mainly mediated by gasdermin, was found to be responsible for podocyte injury in MN in our recent work. Objectives: The aim of this study was to explore the therapeutic effect of an FDA-approved drug, disulfiram (DSF), in the treatment of MN by inhibiting pyroptosis. Methods and Results: DSF significantly alleviated C3a/C5a-induced podocyte injury in vitro and renal lesions in passive Heymann nephritis (PHN) rats, as reflected by the decreased percentage of propidium iodide staining podocytes, decreased lactate dehydrogenase release from cultured podocytes and improvement in 24-h urine protein, serum albumin, serum creatinine, abnormal alterations of podocyte injury markers Desmin and WT-1 and podocyte foot process fusion in PHN rats. The protective effect of DSF on podocyte injury in vitro and in vivo can be ascribed to its inhibition of the activation and membrane translocation of the pyroptosis executor gasdermin D (GSDMD) in podocytes. DSF also inhibited the increase and activation of the pyroptosis signaling pathway NLRP3-ASC-Caspase-1/IL-18/GSDMD in C3a/C5a-treated podocytes and renal tissue of PHN rats. Conclusion: DSF is a potential drug for MN treatment, and its clinical application needs to be further investigated.

Indexed as

DisulfiramMembranous nephropathyPodocytePyroptosis

Identifiers

PMID36157258
PMCPMC9386405

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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.