Evidence map›Paper›PMID 33936382›Full record

ArticleOxidative medicine and cellular longevity2021

Follistatin-Like 1 Attenuation Suppresses Intervertebral Disc Degeneration in Mice through Interacting with TNF-

Shaoyi Wang, Jianlu Wei, Jie Shi, Qiting He, Xiaocong Zhou, Ximei Gao, Lei Cheng

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
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  9. Identification of miRNA-mRNA Pairs in Relation to TNF-Evidence-based complementary and alternative medicine : eCAM · 2022
    Article
  10. Article
  11. Article
  12. Naringin protects human nucleus pulposus cells against TNF-Oxidative medicine and cellular longevity · 2022
    Article
  13. 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

7 authors at 2 institutions in 1 country.

Shaoyi WangDepartment of Orthopedic, Qilu Hospital, Cheeloo College of Medicine of Shandong University, Jinan, China.
Jianlu WeiDepartment of Orthopedic, Qilu Hospital, Cheeloo College of Medicine of Shandong University, Jinan, China.
Jie ShiDepartment of Orthopedic, Qilu Hospital, Cheeloo College of Medicine of Shandong University, Jinan, China.
Qiting HeDepartment of Orthopedic, Qilu Hospital, Cheeloo College of Medicine of Shandong University, Jinan, China.
Xiaocong ZhouShandong Qianfoshan Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China.
Ximei GaoDepartment of International Medicine, Qilu Hospital of Shandong University, Jinan, China.ORCID https://orcid.org/0000-0002-1080-9618
Lei ChengDepartment of Orthopedic, Qilu Hospital, Cheeloo College of Medicine of Shandong University, Jinan, China.ORCID https://orcid.org/0000-0002-5948-1342
Shandong University · CNQilu Hospital of Shandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInflammation plays an important role in intervertebral disc degeneration (IDD). The protein follistatin-like 1 (FSTL1) plays a proinflammatory role in a variety of inflammatory diseases.

objectivesThe purpose of this study was to investigate whether IDD could be delayed by inhibiting FSTL-1 expression.

methodsWe established a puncture-induced IDD model in wild-type and FSTL-1+/- mice and collected intervertebral discs (IVDs) from the mice. Safranin O staining was used to detect cartilage loss of IVD tissue, and HE staining was used to detect morphological changes of IVD tissue. We measured the expression of FSTL-1 and related inflammatory indicators in IVD tissues by immunohistochemical staining, real-time PCR, and Western blotting.

resultsIn the age-induced model of IDD, the level of FSTL-1 increased with the exacerbation of degeneration. In the puncture-induced IDD model, FSTL-1-knockdown mice showed a reduced degree of degeneration compared with that of wild-type mice. Further experiments showed that FSTL-1 knockdown also significantly reduced the level of related inflammatory factors in IVD. In vitro experiments showed that FSTL-1 knockdown significantly reduced TNF-

conclusionKnockdown of FSTL-1 attenuated inflammation by inhibiting the TNF-

Indexed as

AnimalsApoptosis Regulatory ProteinsDisease Models, AnimalFollistatinHumansIntervertebral Disc DegenerationMaleMiceMitochondrial ProteinsSignal TransductionTumor Necrosis Factor-alphaApoptosis Regulatory ProteinsDIABLO protein, humanFollistatinMitochondrial ProteinsTumor Necrosis Factor-alpha

Identifiers

PMID33936382
PMCPMC8055391
OpenAlexW3155293044

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Registered trials

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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.