Evidence map›Paper›PMID 35347118›Full record

ArticleCell death & disease2022

Hepatic deficiency of selenoprotein S exacerbates hepatic steatosis and insulin resistance.

Lu Qiao, Lili Men, Shanshan Yu, Junjie Yao, Yu Li, Mingming Wang, Ying Yu, Ning Wang, Liyuan Ran, Yingjie Wu and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

30 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. SNRK modulates mTOR-autophagy pathway for liver lipid homeostasis in MAFLD.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  17. MOR23 deficiency exacerbates hepatic steatosis in mice.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article
  18. Article
  19. Review
  20. 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

11 authors at 1 institution in 2 countries.

Lu Qiao *Department of Endocrinology, the First Affiliated Hospital of Dalian Medical University, Dalian, China.ORCID 0000-0002-4119-2585
Lili Men *Department of Endocrinology, the First Affiliated Hospital of Dalian Medical University, Dalian, China.
Shanshan YuDepartment of Endocrinology, the First Affiliated Hospital of Dalian Medical University, Dalian, China.
Junjie YaoDepartment of Endocrinology, the First Affiliated Hospital of Dalian Medical University, Dalian, China.
Yu LiDepartment of Endocrinology, the First Affiliated Hospital of Dalian Medical University, Dalian, China.
Mingming WangDepartment of Endocrinology, the First Affiliated Hospital of Dalian Medical University, Dalian, China.
Ying YuDepartment of Endocrinology, the First Affiliated Hospital of Dalian Medical University, Dalian, China.
Ning WangInstitute for Genome Engineered Animal Models of Human Diseases, Dalian Medical University, Dalian, China.
Liyuan RanInstitute for Genome Engineered Animal Models of Human Diseases, Dalian Medical University, Dalian, China.
Yingjie WuInstitute for Genome Engineered Animal Models of Human Diseases, Dalian Medical University, Dalian, China. yingjiewu@dmu.edu.cn.ORCID 0000-0002-2694-1971
Jianling DuDepartment of Endocrinology, the First Affiliated Hospital of Dalian Medical University, Dalian, China. dujianlingcn@163.com.ORCID 0000-0001-9042-6969
Dalian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nonalcoholic fatty liver disease (NAFLD) is closely associated with insulin resistance (IR) and type 2 diabetes mellitus (T2DM), which are all complex metabolic disorders. Selenoprotein S (SelS) is an endoplasmic reticulum (ER) resident selenoprotein involved in regulating ER stress and has been found to participate in the occurrence and development of IR and T2DM. However, the potential role and mechanism of SelS in NAFLD remains unclear. Here, we analyzed SelS expression in the liver of high-fat diet (HFD)-fed mice and obese T2DM model (db/db) mice and generated hepatocyte-specific SelS knockout (SelS

Indexed as

Diabetes Mellitus, Type 2Insulin ResistanceNon-alcoholic Fatty Liver DiseaseAnimalsDiet, High-FatFatty AcidsInsulinLiverMiceMice, Inbred C57BLFatty AcidsInsulin

Identifiers

PMID35347118
PMCPMC8960781
OpenAlexW4220659020

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.