Evidence map›Paper›PMID 35440754›Full record

ArticleExperimental & molecular medicine2022

Grem1 accelerates nucleus pulposus cell apoptosis and intervertebral disc degeneration by inhibiting TGF-β-mediated Smad2/3 phosphorylation.

Shunlun Chen, Linchuan Lei, Zemin Li, Fan Chen, Yuming Huang, Guowei Jiang, Xingyu Guo, Zhuoyang Zhao, Hui Liu, Hua Wang and 3 more

Open access · goldAbstract read
In one paragraph

Article in Experimental & molecular medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
13.5field-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

63 citing papers in PubMed, 102 citations in OpenAlex.

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3 more citing papers are in PubMed but not listed here.

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

13 authors at 2 institutions in 1 country.

Shunlun Chen *Department of Spine Surgery, The First Affiliated Hospital of Sun Yat-sen University, 510080, Guangzhou, China.
Linchuan Lei *Department of Spine Surgery, The First Affiliated Hospital of Sun Yat-sen University, 510080, Guangzhou, China.
Zemin Li *Department of Spine Surgery, The First Affiliated Hospital of Sun Yat-sen University, 510080, Guangzhou, China.
Fan ChenDepartment of Spine Surgery, The First Affiliated Hospital of Sun Yat-sen University, 510080, Guangzhou, China.
Yuming HuangDepartment of Spine Surgery, The First Affiliated Hospital of Sun Yat-sen University, 510080, Guangzhou, China.
Guowei JiangDepartment of Spine Surgery, The First Affiliated Hospital of Sun Yat-sen University, 510080, Guangzhou, China.
Xingyu GuoDepartment of Spine Surgery, The First Affiliated Hospital of Sun Yat-sen University, 510080, Guangzhou, China.
Zhuoyang ZhaoDepartment of Spine Surgery, The First Affiliated Hospital of Sun Yat-sen University, 510080, Guangzhou, China.
Hui LiuDepartment of Spine Surgery, The First Affiliated Hospital of Sun Yat-sen University, 510080, Guangzhou, China.
Hua WangDepartment of Spine Surgery, The First Affiliated Hospital of Sun Yat-sen University, 510080, Guangzhou, China.ORCID http://orcid.org/0000-0002-2605-5697
Caijun LiuDepartment of Spine Surgery, The Third Affiliated Hospital of Guangzhou University of Traditional Chinese Medicine, 510378, Guangzhou, China.
Zhaomin ZhengDepartment of Spine Surgery, The First Affiliated Hospital of Sun Yat-sen University, 510080, Guangzhou, China. zhzhaom@mail.sysu.edu.cn.
Jianru WangDepartment of Spine Surgery, The First Affiliated Hospital of Sun Yat-sen University, 510080, Guangzhou, China. wangjru@mail.sysu.edu.cn.ORCID http://orcid.org/0000-0002-9747-0652
Sun Yat-sen University · CNThe Third Affiliated Hospital of Guangzhou University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intervertebral disc degeneration (IVDD) is a main cause of low back pain, and inflammatory factors play key roles in its pathogenesis. Gremlin-1 (Grem1) was reported to induce an inflammatory response in other fields. This study aimed to investigate the mechanisms of Grem1 in the degenerative process of intervertebral discs. Dysregulated genes were determined by analyzing microarray profiles. The expression of Grem1 in 17 human disc samples (male:female = 9:8) and rat models (n = 5 each group) was measured by western blotting (WB), real-time quantitative PCR (RT-qPCR), and immunohistochemistry (IHC). The regulatory effects of Grem1 on apoptosis were examined using siRNAs, flow cytometry, immunofluorescence (IF), and WB. The therapeutic effect was evaluated by locally injecting specific Grem1 siRNA into IVDD rats. The expression of Grem1 was significantly increased in human degenerative intervertebral discs; furthermore, the expression of Grem1 positively correlated with the level of intervertebral disc degeneration. Grem1 was significantly overexpressed in tumor necrosis factor (TNF)-α-induced degenerative NP cells. Apoptosis in degenerative NP cells transfected with siRNA targeting Grem1 was significantly lower than that in the control group. Specific Grem1 siRNA markedly repressed the development of IVDD in surgery-induced IVDD rats. These results indicated that the expression of Grem1 was positively correlated with the severity of intervertebral disc degeneration, and Grem1 siRNA could inhibit Grem1-induced apoptosis and extracellular matrix alterations by mediating the TGF-β/Smad signaling pathway. This study may provide a therapeutic strategy for alleviating inflammation-induced apoptosis associated with intervertebral disc degeneration.

Indexed as

Intervertebral Disc DegenerationNucleus PulposusAnimalsApoptosisCytokinesFemaleMalePhosphorylationRatsRNA, Small InterferingTumor Necrosis Factor-alphaCytokinesGrem1 protein, ratRNA, Small InterferingTumor Necrosis Factor-alpha

Identifiers

PMID35440754
PMCPMC9076866
OpenAlexW4224296098

What Socratic holds

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LicenceCC BY
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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 Socratic graph.