Evidence map›Paper›PMID 30728376›Full record

ArticleScientific reports2019

Network-based integrated analysis of omics data reveal novel players of TGF-β1-induced EMT in human peritoneal mesothelial cells.

Soo Min Han, Hye-Myung Ryu, Jinjoo Suh, Kong-Joo Lee, Soon-Youn Choi, Sangdun Choi, Yong-Lim Kim, Joo Young Huh, Hunjoo Ha

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 20% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
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  5. Review
  6. WT1 in Adipose Tissue: From Development to Adult Physiology.Frontiers in cell and developmental biology · 2022
    Review
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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 at 4 institutions in 1 country.

Soo Min HanGraduate School of Pharmaceutical Sciences, College of Pharmacy, Ewha Womans University, Seoul, Republic of Korea.
Hye-Myung RyuDepartment of Internal Medicine, School of Medicine, Kyungpook National University, Seoul, Republic of Korea.
Jinjoo SuhGraduate School of Pharmaceutical Sciences, College of Pharmacy, Ewha Womans University, Seoul, Republic of Korea.
Kong-Joo LeeGraduate School of Pharmaceutical Sciences, College of Pharmacy, Ewha Womans University, Seoul, Republic of Korea.
Soon-Youn ChoiDepartment of Internal Medicine, School of Medicine, Kyungpook National University, Seoul, Republic of Korea.
Sangdun ChoiDepartment of Molecular Science and Technology, Ajou University, Suwon, Republic of Korea.
Yong-Lim KimDepartment of Internal Medicine, School of Medicine, Kyungpook National University, Seoul, Republic of Korea. ylkim@knu.ac.kr.
Joo Young HuhCollege of Pharmacy, Chonnam National University, Gwangju, Republic of Korea. jooyhuh@jnu.ac.kr.
Hunjoo HaGraduate School of Pharmaceutical Sciences, College of Pharmacy, Ewha Womans University, Seoul, Republic of Korea.
Ewha Womans University · KRKyungpook National University · KRAjou University · KRChonnam National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long-term peritoneal dialysis is associated with progressive fibrosis of the peritoneum. Epithelial-mesenchymal transition (EMT) of mesothelial cells is an important mechanism involved in peritoneal fibrosis, and TGF-β1 is considered central in this process. However, targeting currently known TGF-β1-associated pathways has not proven effective to date. Therefore, there are still gaps in understanding the mechanisms underlying TGF-β1-associated EMT and peritoneal fibrosis. We conducted network-based integrated analysis of transcriptomic and proteomic data to systemically characterize the molecular signature of TGF-β1-stimulated human peritoneal mesothelial cells (HPMCs). To increase the power of the data, multiple expression datasets of TGF-β1-stimulated human cells were employed, and extended based on a human functional gene network. Dense network sub-modules enriched with differentially expressed genes by TGF-β1 stimulation were prioritized and genes of interest were selected for functional analysis in HPMCs. Through integrated analysis, ECM constituents and oxidative stress-related genes were shown to be the top-ranked genes as expected. Among top-ranked sub-modules, TNFAIP6, ZC3H12A, and NNT were validated in HPMCs to be involved in regulation of E-cadherin, ZO-1, fibronectin, and αSMA expression. The present data shows the validity of network-based integrated analysis in discovery of novel players in TGF-β1-induced EMT in peritoneal mesothelial cells, which may serve as new prognostic markers and therapeutic targets for peritoneal dialysis patients.

Indexed as

ActinsAntigens, CDCadherinsCells, CulturedEpithelial CellsEpithelial-Mesenchymal TransitionEpitheliumFibronectinsHumansPeritoneal DialysisPeritoneal FibrosisPeritoneumProteomicsRepublic of KoreaSignal TransductionTransforming Growth Factor beta1ACTA2 protein, humanActinsAntigens, CDCadherinsCDH1 protein, humanFibronectinsFN1 protein, humanTransforming Growth Factor beta1

Identifiers

PMID30728376
PMCPMC6365569
OpenAlexW2914723063

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.