Evidence map›Paper›PMID 37815699›Full record

ArticleScience China. Life sciences2024

Melatonin decreases GSDME mediated mesothelial cell pyroptosis and prevents peritoneal fibrosis and ultrafiltration failure.

Hongxia Ruan, Xuejuan Li, Lina Zhou, Zihan Zheng, Rulin Hua, Xu Wang, Yuan Wang, Yujie Fan, Shuwen Guo, Lihua Wang and 17 more

Abstract read
PubMed Publisher
In one paragraph

Article in Science China. Life sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.8field-weighted citation impact, top 14% of its field
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

10 citing papers in PubMed, 12 citations in OpenAlex.

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  10. Calcium signaling-mediated transcriptional reprogramming during abiotic stress response in plants.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2023
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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

27 authors at 6 institutions in 1 country.

Hongxia Ruan *Advanced Institute for Medical Sciences, Dalian Medical University, Dalian, 116044, China.
Xuejuan Li *Department of Nephrology, Second Hospital, Dalian Medical University, Dalian, 116023, China. clairesnow@126.com.
Lina Zhou *CAS Key Laboratory of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, 116023, China.
Zihan ZhengChongqing International Institute for Immunology, Chongqing, 401320, China.
Rulin HuaAdvanced Institute for Medical Sciences, Dalian Medical University, Dalian, 116044, China.
Xu WangDepartment of Nephrology, Shenzhen Hospital, Southern Medical University, Shenzhen, 518101, China.
Yuan WangAdvanced Institute for Medical Sciences, Dalian Medical University, Dalian, 116044, China.
Yujie FanAdvanced Institute for Medical Sciences, Dalian Medical University, Dalian, 116044, China.
Shuwen GuoAdvanced Institute for Medical Sciences, Dalian Medical University, Dalian, 116044, China.
Lihua WangDepartment of Nephrology, Second Hospital, Dalian Medical University, Dalian, 116023, China.
Shafiq Ur RahmanAdvanced Institute for Medical Sciences, Dalian Medical University, Dalian, 116044, China.
Ziwei WangAdvanced Institute for Medical Sciences, Dalian Medical University, Dalian, 116044, China.
Yuyuan WeiAdvanced Institute for Medical Sciences, Dalian Medical University, Dalian, 116044, China.
Shuangyan YuDepartment of Nephrology, Second Hospital, Dalian Medical University, Dalian, 116023, China.
Rongzhi ZhangDepartment of Nephrology, Second Hospital, Dalian Medical University, Dalian, 116023, China.
Qian ChengDepartment of Nephrology, Second Hospital, Dalian Medical University, Dalian, 116023, China.
Jie ShengDepartment of Nephrology, Second Hospital, Dalian Medical University, Dalian, 116023, China.
Xue LiDepartment of Nephrology, Second Hospital, Dalian Medical University, Dalian, 116023, China.
Xiaoyan LiuDepartment of Nephrology, Second Hospital, Dalian Medical University, Dalian, 116023, China.
Ruqiang YuanAdvanced Institute for Medical Sciences, Dalian Medical University, Dalian, 116044, China.
Xiaoyan ZhangWuhu Hospital and Health Science Center, East China Normal University, Shanghai, 200241, China.
Lihong ChenAdvanced Institute for Medical Sciences, Dalian Medical University, Dalian, 116044, China.
Guowang XuCAS Key Laboratory of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, 116023, China.
Youfei GuanAdvanced Institute for Medical Sciences, Dalian Medical University, Dalian, 116044, China.
Jing NiePeking University First Hospital, Peking University, Beijing, 100034, China.
Hongqiang QinCAS Key Laboratory of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, 116023, China. qinhq@dicp.ac.cn.
Feng ZhengAdvanced Institute for Medical Sciences, Dalian Medical University, Dalian, 116044, China. zhengfeng@dmu.edu.cn.
Dalian Medical University · CNChinese Academy of Sciences · CNEast China Normal University · CNSecond Affiliated Hospital of Dalian Medical University · CNDalian Institute of Chemical Physics · CNPeking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peritoneal fibrosis together with increased capillaries is the primary cause of peritoneal dialysis failure. Mesothelial cell loss is an initiating event for peritoneal fibrosis. We find that the elevated glucose concentrations in peritoneal dialysate drive mesothelial cell pyroptosis in a manner dependent on caspase-3 and Gasdermin E, driving downstream inflammatory responses, including the activation of macrophages. Moreover, pyroptosis is associated with elevated vascular endothelial growth factor A and C, two key factors in vascular angiogenesis and lymphatic vessel formation. GSDME deficiency mice are protected from high glucose induced peritoneal fibrosis and ultrafiltration failure. Application of melatonin abrogates mesothelial cell pyroptosis through a MT1R-mediated action, and successfully reduces peritoneal fibrosis and angiogenesis in an animal model while preserving dialysis efficacy. Mechanistically, melatonin treatment maintains mitochondrial integrity in mesothelial cells, meanwhile activating mTOR signaling through an increase in the glycolysis product dihydroxyacetone phosphate. These effects together with quenching free radicals by melatonin help mesothelial cells maintain a relatively stable internal environment in the face of high-glucose stress. Thus, Melatonin treatment holds some promise in preserving mesothelium integrity and in decreasing angiogenesis to protect peritoneum function in patients undergoing peritoneal dialysis.

Indexed as

MelatoninPeritoneal FibrosisAnimalsEpithelial CellsFibrosisGlucoseHumansMicePyroptosisUltrafiltrationVascular Endothelial Growth Factor AGlucoseMelatoninVascular Endothelial Growth Factor AGSDMEmelatoninmitochondriamTORperitoneal fibrosispyroptosis

Identifiers

PMID37815699
OpenAlexW4387473053

What OpenQuestion 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 OpenQuestion graph.