Evidence map›Paper›PMID 29531531›Full record

ArticleStem cells international2018

Inflammatory Stimuli Significantly Change the miRNA Profile of Human Adipose-Derived Stem Cells.

Zicheng Wang, Haili Li, Li Cheng, Zhongyuan Zhang, Hao Wang, Tongde Lv, Jian Lin, Liqun Zhou

Open access · goldAbstract read
In one paragraph

Article in Stem cells international, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.1field-weighted citation impact, top 60% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

8 authors at 1 institution in 1 country.

Zicheng WangDepartment of Urology, Peking University First Hospital, Beijing 100034, China.ORCID 0000-0002-1291-2168
Haili LiDepartment of Ophthalmology, Peking University First Hospital, Beijing 100034, China.ORCID 0000-0002-8394-9793
Li ChengDepartment of Urology, Peking University First Hospital, Beijing 100034, China.
Zhongyuan ZhangDepartment of Urology, Peking University First Hospital, Beijing 100034, China.ORCID 0000-0002-8065-0198
Hao WangDepartment of Obstetrics and Gynaecology, Peking University First Hospital, Beijing 100034, China.ORCID 0000-0001-9501-1885
Tongde LvDepartment of Urology, Peking University First Hospital, Beijing 100034, China.ORCID 0000-0002-1660-543X
Jian LinDepartment of Urology, Peking University First Hospital, Beijing 100034, China.ORCID 0000-0003-3476-5792
Liqun ZhouDepartment of Urology, Peking University First Hospital, Beijing 100034, China.ORCID 0000-0002-3862-5319
Peking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHuman adipose-derived stem cells (hASCs) have been shown to have immunoregulatory properties in many studies. However, the mechanisms remain unknown. miRNAs are associated with many cellular processes, including immune responses. Thus, we hypothesized that miRNAs act as immunoregulators when hASCs are stimulated by inflammatory environments.

methodsA set of cytokines was used to stimulate the hASCs in the cytokine group, while no cytokines were used to stimulate the cells in the normal group. A microarray was used to obtain the miRNA expression profile of hASCs, and RT-PCR was used to validate the miRNAs that were differentially expressed between the two groups. Target genes were predicted using online databases, and KEGG analysis was performed to identify the pathways enriched by the target genes of all the differentially expressed miRNAs.

resultsFive miRNAs were significantly upregulated, and 2 miRNAs were downregulated in the cytokine group compared with the normal group. We identified several immune-related pathways that are targeted individually or collectively by those miRNAs.

conclusionInflammatory stimuli changed the miRNA expression profile of hASCs. miRNAs may play a pivotal role in the immune response in hASCs and may be targets through which the immunoregulatory functions of hASCs can be enhanced.

Identifiers

PMID29531531
PMCPMC5829350
OpenAlexW2787829448

What OpenQuestion holds

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LicenceCC BY
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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.