Evidence map›Paper›PMID 35046894›Full record

ArticleFrontiers in endocrinology2021

Upregulation of T Cell Receptor Signaling Pathway Components in Gestational Diabetes Mellitus Patients: Joint Analysis of mRNA and circRNA Expression Profiles.

Yan-Ming Chen, Qiong Zhu, Jie Cai, Zhi-Jia Zhao, Bin-Bin Yao, Li-Ming Zhou, Lin-Dan Ji, Jin Xu

Open access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

  1. Trial
  2. Article
  3. Longitudinal associations between PMFrontiers in cellular and infection microbiology · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Circular RNA hsa_circ_0002268 (International journal of molecular sciences · 2024
    Article
  9. Article
  10. Review
  11. Article
  12. Integrated bioinformatics andFrontiers in nutrition · 2022
    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

8 authors at 1 institution in 1 country.

Yan-Ming ChenDepartment of Science and Education, Affiliated People's Hospital of Ningbo University, Ningbo, China.
Qiong ZhuDepartment of Pediatrics, Affiliated People's Hospital of Ningbo University, Ningbo, China.
Jie CaiDepartment of Reproductive Medicine, Ningbo Women and Children's Hospital, Ningbo, China.
Zhi-Jia ZhaoDepartment of Preventive Medicine, School of Medicine, Ningbo University, Ningbo, China.
Bin-Bin YaoDepartment of Preventive Medicine, School of Medicine, Ningbo University, Ningbo, China.
Li-Ming ZhouDepartment of Reproductive Medicine, Ningbo Women and Children's Hospital, Ningbo, China.
Lin-Dan JiDepartment of Science and Education, Affiliated People's Hospital of Ningbo University, Ningbo, China.
Jin XuDepartment of Preventive Medicine, School of Medicine, Ningbo University, Ningbo, China.
Ningbo University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Gestational diabetes mellitus (GDM) is one of the most common complications of pregnancy, and its pathogenesis is still unclear. Studies have shown that circular RNAs (circRNAs) can regulate blood glucose levels by targeting mRNAs, but the role of circRNAs in GDM is still unknown. Therefore, a joint microarray analysis of circRNAs and their target mRNAs in GDM patients and healthy pregnant women was carried out. Methods: In this study, microarray analyses of mRNA and circRNA in 6 GDM patients and 6 healthy controls were conducted to identify the differentially expressed mRNA and circRNA in GDM patients, and some of the discovered mRNAs and circRNAs were further validated in additional 56 samples by quantitative realtime PCR (qRT-PCR) and droplet digital PCR (ddPCR). Results: Gene ontology and pathway analyses showed that the differentially expressed genes were significantly enriched in T cell immune-related pathways. Cross matching of the differentially expressed mRNAs and circRNAs in the top 10 KEGG pathways identified 4 genes ( Conclusion: Upregulation of T cell receptor signaling pathway components may represent the major pathological mechanism underlying GDM, thus providing a potential approach for the prevention and treatment of GDM.

Indexed as

Signal TransductionDiabetes, GestationalFemaleGene OntologyHumansMicroarray AnalysisPregnancyReceptors, Antigen, T-CellRNA, CircularRNA, MessengerUp-RegulationReceptors, Antigen, T-CellRNA, CircularRNA, MessengercircRNAgestational diabetes mellitusmicroarray analysismRNAT cell receptor signaling pathway

Identifiers

PMID35046894
PMCPMC8763273
OpenAlexW4205818454

What OpenQuestion holds

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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.