Evidence map›Paper›PMID 32411720›Full record

ArticleFrontiers in molecular biosciences2020

Molecular Mechanism of Mesenchyme Homeobox 1 in Transforming Growth Factor β1-Induced

Zhiyuan Wei, Chao Han, Haisheng Li, Weifeng He, Junyi Zhou, Hui Dong, Yuzhang Wu, Yi Tian, Gaoxing Luo

Abstract read
In one paragraph

Article in Frontiers in molecular biosciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

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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

9 authors.

Zhiyuan WeiInstitute of Burn Research, PLA, State Key Laboratory of Trauma, Burn and Combined Injury, The First Affiliated Hospital of Third Military Medical University (Army Medical University), Chongqing, China.
Chao HanInstitute of Immunology, PLA, Third Military Medical University (Army Medical University), Chongqing, China.
Haisheng LiInstitute of Burn Research, PLA, State Key Laboratory of Trauma, Burn and Combined Injury, The First Affiliated Hospital of Third Military Medical University (Army Medical University), Chongqing, China.
Weifeng HeInstitute of Burn Research, PLA, State Key Laboratory of Trauma, Burn and Combined Injury, The First Affiliated Hospital of Third Military Medical University (Army Medical University), Chongqing, China.
Junyi ZhouInstitute of Burn Research, PLA, State Key Laboratory of Trauma, Burn and Combined Injury, The First Affiliated Hospital of Third Military Medical University (Army Medical University), Chongqing, China.
Hui DongInstitute of Immunology, PLA, Third Military Medical University (Army Medical University), Chongqing, China.
Yuzhang WuInstitute of Immunology, PLA, Third Military Medical University (Army Medical University), Chongqing, China.
Yi TianInstitute of Immunology, PLA, Third Military Medical University (Army Medical University), Chongqing, China.
Gaoxing LuoInstitute of Burn Research, PLA, State Key Laboratory of Trauma, Burn and Combined Injury, The First Affiliated Hospital of Third Military Medical University (Army Medical University), Chongqing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Organ fibrosis is characterized by excessive fibroblast, and extracellular matrix and the molecular basis are not fully elucidated. Recent studies have proven that P311, an 8-kDa conserved protein, could promote various organ fibrosis, such as skin, kidney, liver, and lung, partially through upregulating transforming growth factor β1 (TGF-β1) translation. However, the upstream regulators and mechanism of P311 gene regulation remain unclear, although we previously found that cytokines, hypoxia, and TGF-β1 could upregulate P311 transcription. Here, we aimed to elucidate the molecular mechanism of TGF-β1-induced P311 transcriptional regulation, focusing on mesenchyme homeobox 1 (Meox1). In this article, we identified the core promoter of P311 through bioinformatics analysis and luciferase reporter assays. Moreover, we demonstrated that Meox1, induced by TGF-β1, could bind to the promoter of P311 and promote its transcriptional activity. Furthermore, the effect of Meox1 on P311 transcriptional expression contributed to altered migration and proliferation in human dermal fibroblast cells. In conclusion, we identified Meox1 as a novel transcription factor of P311 gene, providing a new clue of the pathogenesis in fibrosis.

Indexed as

fibrosisMeox1P311promotertranscription factor

Identifiers

PMID32411720
PMCPMC7199492

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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.