Evidence map›Paper›PMID 37483618›Full record

ReviewFrontiers in immunology2023

Sirtuin family in autoimmune diseases.

Zhengjie Tao, Zihan Jin, Jiabiao Wu, Gaojun Cai, Xiaolong Yu

Erratum issuedOpen access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 53 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed, 1 pooled it
11.2field-weighted citation impact, top 1% 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

53 citing papers in PubMed, 1 synthesis or guideline pooled it, 63 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. SIRT3-Dependent Actions of Berberine: From Molecular Therapies to Toxicity.Journal of biochemical and molecular toxicology · 2026
    Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Skin Cancer Prevention and Antiaging: Role of Nicotinamide.International journal of molecular sciences · 2026
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. [Histone deacetylases and alcohol-related liver disease].Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2026
    Review
  15. Article
  16. Article
  17. NMN protects cisplatin-associated AKI via NADFrontiers in immunology · 2026
    Article
  18. Review
  19. Article
  20. Diabetic keratopathy and nuclear proteins (Review).Molecular medicine reports · 2026
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 1 country.

Zhengjie TaoScience and Education Section, Wujin Hospital Affiliated with Jiangsu University, Changzhou, Jiangsu, China.
Zihan JinClinical Lab, Changzhou Second People's Hospital Affiliated to Nanjing Medical University, Changzhou, China.
Jiabiao WuDepartment of Immunology, Wujin Hospital Affiliated with Jiangsu University, Changzhou, Jiangsu, China.
Gaojun CaiCardiology, Wujin Hospital Affiliated with Jiangsu University, Changzhou, Jiangsu, China.
Xiaolong YuScience and Education Section, Wujin Hospital Affiliated with Jiangsu University, Changzhou, Jiangsu, China.
Jiangsu University · CNNanjing Medical University · CNXuzhou Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In recent years, epigenetic modifications have been widely researched. As humans age, environmental and genetic factors may drive inflammation and immune responses by influencing the epigenome, which can lead to abnormal autoimmune responses in the body. Currently, an increasing number of studies have emphasized the important role of epigenetic modification in the progression of autoimmune diseases. Sirtuins (SIRTs) are class III nicotinamide adenine dinucleotide (NAD)-dependent histone deacetylases and SIRT-mediated deacetylation is an important epigenetic alteration. The SIRT family comprises seven protein members (namely, SIRT1-7). While the catalytic core domain contains amino acid residues that have remained stable throughout the entire evolutionary process, the N- and C-terminal regions are structurally divergent and contribute to differences in subcellular localization, enzymatic activity and substrate specificity. SIRT1 and SIRT2 are localized in the nucleus and cytoplasm. SIRT3, SIRT4, and SIRT5 are mitochondrial, and SIRT6 and SIRT7 are predominantly found in the nucleus. SIRTs are key regulators of various physiological processes such as cellular differentiation, apoptosis, metabolism, ageing, immune response, oxidative stress, and mitochondrial function. We discuss the association between SIRTs and common autoimmune diseases to facilitate the development of more effective therapeutic strategies.

Indexed as

Sirtuin 3SirtuinsAgingEpigenesis, GeneticHumansOxidative StressSirtuin 1SIRT6 protein, humanSirtuin 1Sirtuin 3Sirtuinsautoimmune diseasesimmune inflammationoxidative stressreviewsirtuinstreatment

Identifiers

PMID37483618
PMCPMC10357840
OpenAlexW4383377664

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.