Evidence map›Paper›PMID 36323699›Full record

ArticleNature communications2022

Phosphorylation of 17β-hydroxysteroid dehydrogenase 13 at serine 33 attenuates nonalcoholic fatty liver disease in mice.

Wen Su, Sijin Wu, Yongliang Yang, Yanlin Guo, Haibo Zhang, Jie Su, Lei Chen, Zhuo Mao, Rongfeng Lan, Rong Cao and 15 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

25 citing papers in PubMed, 47 citations in OpenAlex.

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  11. Liver lipid droplet cholesterol content is a key determinant of metabolic dysfunction-associated steatohepatitis.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  12. Article
  13. Article
  14. Genetics of Metabolic Dysfunction-associated Steatotic Liver Disease: The State of the Art Update.Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · 2024
    Review
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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

25 authors at 8 institutions in 1 country.

Wen SuDepartment of Pathophysiology, Shenzhen University, Shenzhen, 518060, China. suwen@szu.edu.cn.ORCID 0000-0001-5576-1286
Sijin WuState Key Laboratory of Molecular Reaction Dynamics, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, 116024, China.
Yongliang YangLaboratoy of Innovative Drug Discovery, School of Bioengineering, Dalian University of Technology, Dalian, 116023, China.ORCID 0000-0003-0449-0599
Yanlin GuoHealth Science Center, East China Normal University, Shanghai, 200241, China.ORCID 0000-0003-4422-3954
Haibo ZhangAdvanced Institute for Medical Sciences, Dalian Medical University, Dalian, 116044, China.ORCID 0000-0003-1755-1813
Jie SuDepartment of Pathophysiology, Shenzhen University, Shenzhen, 518060, China.
Lei ChenDepartment of Pathophysiology, Shenzhen University, Shenzhen, 518060, China.ORCID 0000-0001-5395-5909
Zhuo MaoShenzhen University Health Science Center, Shenzhen University, Shenzhen, 518060, China.
Rongfeng LanShenzhen University Health Science Center, Shenzhen University, Shenzhen, 518060, China.ORCID 0000-0003-2124-7232
Rong CaoDepartment of Nephrology, The First Affiliated Hospital of Shenzhen University, Shenzhen, 518035, China.
Chunjiong WangDepartment of Physiology and Pathophysiology, The Province and Ministry Co-sponsored Collaborative Innovation Center for Medical Epigenetics, Tianjin Medical University, Tianjin, China.
Hu XuAdvanced Institute for Medical Sciences, Dalian Medical University, Dalian, 116044, China.
Cong ZhangAdvanced Institute for Medical Sciences, Dalian Medical University, Dalian, 116044, China.ORCID 0000-0003-4284-938X
Sha LiMedical College, Hebei University of Engineering, Handan, China.
Min GaoShenzhen University Health Science Center, Shenzhen University, Shenzhen, 518060, China.ORCID 0000-0003-2147-331X
Xiaocong ChenShenzhen University Health Science Center, Shenzhen University, Shenzhen, 518060, China.ORCID 0000-0003-1963-2369
Zhiyou ZhengShenzhen University Health Science Center, Shenzhen University, Shenzhen, 518060, China.ORCID 0000-0002-7351-0955
Bing WangAdvanced Institute for Medical Sciences, Dalian Medical University, Dalian, 116044, China.
Yi'ao LiuShenzhen University Health Science Center, Shenzhen University, Shenzhen, 518060, China.ORCID 0000-0003-1857-1023
Zuojun LiuShenzhen University Health Science Center, Shenzhen University, Shenzhen, 518060, China.
Zimei WangShenzhen University Health Science Center, Shenzhen University, Shenzhen, 518060, China.
Baohua LiuShenzhen University Health Science Center, Shenzhen University, Shenzhen, 518060, China.ORCID 0000-0002-1599-8059
Xinmin FanDepartment of Pathophysiology, Shenzhen University, Shenzhen, 518060, China.
Xiaoyan ZhangHealth Science Center, East China Normal University, Shanghai, 200241, China. wserien@163.com.ORCID 0000-0002-4060-2423
Youfei GuanAdvanced Institute for Medical Sciences, Dalian Medical University, Dalian, 116044, China. guanyf@dmu.edu.cn.ORCID 0000-0002-5231-0209
Shenzhen University Health Science Center · CNDalian Medical University · CNShenzhen University · CNEast China Normal University · CNDalian Institute of Chemical Physics · CNDalian University of Technology · CNHebei University of Engineering · CNTianjin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

17β-hydroxysteroid dehydrogenase-13 is a hepatocyte-specific, lipid droplet-associated protein. A common loss-of-function variant of HSD17B13 (rs72613567: TA) protects patients against non-alcoholic fatty liver disease with underlying mechanism incompletely understood. In the present study, we identify the serine 33 of 17β-HSD13 as an evolutionally conserved PKA target site and its phosphorylation facilitates lipolysis by promoting its interaction with ATGL on lipid droplets. Targeted mutation of Ser33 to Ala (S33A) decreases ATGL-dependent lipolysis in cultured hepatocytes by reducing CGI-58-mediated ATGL activation. Importantly, a transgenic knock-in mouse strain carrying the HSD17B13 S33A mutation (HSD17B13

Indexed as

Non-alcoholic Fatty Liver Disease17-Hydroxysteroid DehydrogenasesAnimalsHepatocytesLiverMicePhosphorylationSerine17-Hydroxysteroid Dehydrogenases3 (or 17)-beta-hydroxysteroid dehydrogenaseSerine

Identifiers

PMID36323699
PMCPMC9630536
OpenAlexW4308149416

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.