Evidence map›Paper›PMID 33510050›Full record

ArticleMolecules and cells2021

Transforming Growth Factor β Inhibits MUC5AC Expression by Smad3/HDAC2 Complex Formation and NF-κB Deacetylation at K310 in NCI-H292 Cells.

Su Ui Lee, Mun-Ock Kim, Myung-Ji Kang, Eun Sol Oh, Hyunju Ro, Ro Woon Lee, Yu Na Song, Sunin Jung, Jae-Won Lee, Soo Yun Lee and 3 more

Open access · diamondAbstract read
In one paragraph

Article in Molecules and cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Multifaceted mechanistic exploration ofFrontiers in cell and developmental biology · 2026
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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

13 authors at 2 institutions in 1 country.

Su Ui LeeNatural Medicine Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Cheongju 28116, Korea.ORCID https://orcid.org/0000-0002-6455-5414
Mun-Ock KimNatural Medicine Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Cheongju 28116, Korea.ORCID https://orcid.org/0000-0003-3722-5724
Myung-Ji KangNatural Medicine Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Cheongju 28116, Korea.ORCID https://orcid.org/0000-0003-0326-2156
Eun Sol OhNatural Medicine Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Cheongju 28116, Korea.ORCID https://orcid.org/0000-0002-0313-4747
Hyunju RoDepartment of Biological Sciences, College of Bioscience and Biotechnology, Chungnam National University, Daejeon 34134, Korea.ORCID https://orcid.org/0000-0002-0829-9639
Ro Woon LeeNatural Medicine Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Cheongju 28116, Korea.ORCID https://orcid.org/0000-0002-3195-9762
Yu Na SongNatural Medicine Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Cheongju 28116, Korea.ORCID https://orcid.org/0000-0001-7056-9428
Sunin JungNatural Medicine Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Cheongju 28116, Korea.ORCID https://orcid.org/0000-0003-0731-1613
Jae-Won LeeNatural Medicine Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Cheongju 28116, Korea.ORCID https://orcid.org/0000-0003-0438-6732
Soo Yun LeeImmunotherapy Research Center, KRIBB, Daejeon 34141, Korea.ORCID https://orcid.org/0000-0002-0020-9467
Taeyeol BaeImmunotherapy Research Center, KRIBB, Daejeon 34141, Korea.ORCID https://orcid.org/0000-0001-9499-236X
Sung-Tae HongDepartment of Anatomy & Cell Biology, Department of Medical Science, Chungnam National University College of Medicine, Daejeon 35015, Korea.ORCID https://orcid.org/0000-0001-5981-4859
Tae-Don KimImmunotherapy Research Center, KRIBB, Daejeon 34141, Korea.ORCID https://orcid.org/0000-0002-5910-4264
Korea Research Institute of Bioscience and Biotechnology · KRChungnam National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Airway mucus secretion is an essential innate immune response for host protection. However, overproduction and hypersecretion of mucus, mainly composed of the gel- forming MUC5AC protein, are significant risk factors for patients with asthma and chronic obstructive pulmonary disease (COPD). The transforming growth factor β (TGFβ) signaling pathway negatively regulates MUC5AC expression; however, the underlying molecular mechanism is not fully understood. Here, we showed that TGFβ significantly reduces the expression of

Indexed as

AcetylationCell Line, TumorGene Expression Regulation, NeoplasticHistone Deacetylase 2HumansLysineModels, BiologicalMucin 5ACNF-kappa BPromoter Regions, GeneticSmad3 ProteinTransforming Growth Factor betaHDAC2 protein, humanHistone Deacetylase 2LysineMucin 5ACNF-kappa BSmad3 ProteinTransforming Growth Factor betaHDAC2MUC5ACNF-κBSmad3transforming growth factor β

Identifiers

PMID33510050
PMCPMC7854180
OpenAlexW3121133264

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

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.