Evidence map›Paper›PMID 33780118›Full record

ArticleAging cell2021

Declined miR-181a-5p expression is associated with impaired natural killer cell development and function with aging.

Jiao Lu, Shan Li, Xiaopeng Li, Wenming Zhao, Xuefeng Duan, Xiuling Gu, Jianqiao Xu, Bolan Yu, Luis J Sigal, Zhongjun Dong and 2 more

Open access · goldAbstract read
In one paragraph

Article in Aging cell, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

20 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
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  8. Immunosenescence: signaling pathways, diseases and therapeutic targets.Signal transduction and targeted therapy · 2025
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  11. Expert opinion on therapeutic targets · 2024
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  14. Hypertrophic cardiomyopathy inThe journal of cardiovascular aging · 2024
    Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review
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

12 authors at 5 institutions in 2 countries.

Jiao LuCAS Key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China.
Shan LiCAS Key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China.
Xiaopeng LiCAS Key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China.
Wenming ZhaoCAS Key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China.
Xuefeng DuanCAS Key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China.
Xiuling GuCAS Key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China.
Jianqiao XuDepartment of Respiratory Medicine, Chinese PLA General Hospital, Beijing, China.
Bolan YuKey Laboratory for Major Obstetric Diseases of Guangdong Province, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Luis J SigalDepartment of Microbiology and Immunology, Thomas Jefferson University, Philadelphia, PA, USA.ORCID 0000-0001-6642-5472
Zhongjun DongSchool of Medicine, Tsinghua University, Beijing, China.
Lixin XieDepartment of Respiratory Medicine, Chinese PLA General Hospital, Beijing, China.
Min FangCAS Key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China.ORCID 0000-0002-5278-1430
Chinese Academy of Sciences · CNChinese PLA General Hospital · CNThird Affiliated Hospital of Guangzhou Medical University · CNThomas Jefferson University · USTsinghua University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRNAs) regulate gene expression and thereby influence cell development and function. Numerous studies have shown the significant roles of miRNAs in regulating immune cells including natural killer (NK) cells. However, little is known about the role of miRNAs in NK cells with aging. We previously demonstrated that the aged C57BL/6 mice have significantly decreased proportion of mature (CD27

Indexed as

AgingAnimalsCells, CulturedCytotoxicity, ImmunologicGene Expression RegulationHumansK562 CellsKiller Cells, NaturalMiceMice, Inbred C57BLMicroRNAsProtein Serine-Threonine KinasesProto-Oncogene Proteins c-bcl-2Bcl2 protein, mouseMicroRNAsmirn181 microRNA, mouseMIRN223 microRNA, mouseNlk protein, mouseProtein Serine-Threonine KinasesProto-Oncogene Proteins c-bcl-2agingdevelopmentfunctionMiR-181a-5pMiRNomeNK cells

Identifiers

PMID33780118
PMCPMC8135006
OpenAlexW3147125457

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.