Evidence map›Paper›PMID 25134539›Full record

ArticleMolecules and cells2014

Indacaterol inhibits tumor cell invasiveness and MMP-9 expression by suppressing IKK/NF-κB activation.

Su Ui Lee, Kyung-Seop Ahn, Min Hee Sung, Ji-Won Park, Hyung Won Ryu, Hyun-Jun Lee, Sung-Tae Hong, Sei-Ryang Oh

Open access · diamondAbstract read
In one paragraph

Article in Molecules and cells, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
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  3. 2-Phenethylamines in Medicinal Chemistry: A Review.Molecules (Basel, Switzerland) · 2023
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  10. Synergistic Inhibition of Thalidomide and Icotinib on Human Non-Small Cell Lung Carcinomas Through ERK and AKT Signaling.Medical science monitor : international medical journal of experimental and clinical research · 2018
    Article
  11. Review
  12. Article
  13. Article
  14. Triptolide Inhibits Invasion and Tumorigenesis of Hepatocellular Carcinoma MHCC-97H Cells Through NF-κB Signaling.Medical science monitor : international medical journal of experimental and clinical research · 2016
    Article
  15. 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

8 authors at 2 institutions in 1 country.

Su Ui LeeNatural Medicine Research Center, Korea Research Institute of Bioscience and Biotechnology, Chungbuk 363-883, Korea.
Kyung-Seop AhnNatural Medicine Research Center, Korea Research Institute of Bioscience and Biotechnology, Chungbuk 363-883, Korea.
Min Hee SungNatural Medicine Research Center, Korea Research Institute of Bioscience and Biotechnology, Chungbuk 363-883, Korea.
Ji-Won ParkNatural Medicine Research Center, Korea Research Institute of Bioscience and Biotechnology, Chungbuk 363-883, Korea.
Hyung Won RyuNatural Medicine Research Center, Korea Research Institute of Bioscience and Biotechnology, Chungbuk 363-883, Korea.
Hyun-Jun LeeTargeted Medicine Research Center, Korea Research Institute of Bioscience and Biotechnology, Chungbuk 363-883, Korea.
Sung-Tae HongDepartment of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon 305-701, Korea.
Sei-Ryang OhNatural Medicine Research Center, Korea Research Institute of Bioscience and Biotechnology, Chungbuk 363-883, Korea.
Korea Research Institute of Bioscience and Biotechnology · KRKorea Advanced Institute of Science and Technology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The β2 adrenergic receptor (ADRB2) is a G protein-coupled transmembrane receptor expressed in the human respiratory tract and widely recognized as a pharmacological target for treatments of asthma and chronic obstructive pulmonary disorder (COPD). Although a number of ADRB2 agonists have been developed for use in asthma therapy, indacaterol is the only ultra-long-acting inhaled β2-agonist (LABA) approved by the FDA for relieving the symptoms in COPD patients. The precise molecular mechanism underlying the pharmacological effect of indacaterol, however, remains unclear. Here, we show that β-arrestin-2 mediates the internalization of ADRB2 following indacaterol treatment. Moreover, we demonstrate that indacaterol significantly inhibits tumor necrosis factor-α (TNF-α)-induced NF-κB activity by reducing levels of both phosphorylated-IKK and -IκBα, thereby decreasing NF-κB nuclear translocation and the expression of MMP-9, an NF-κB target gene. Subsequently, we show that indacaterol significantly inhibits TNF-α/NF-κB-induced cell invasiveness and migration in a human cancer cell line. In conclusion, we propose that indacaterol may inhibit NF-κB activity in a β-arrestin2-dependent manner, preventing further lung damage and improving lung function in COPD patients.

Indexed as

Gene Expression Regulation, NeoplasticAdrenergic beta-2 Receptor AgonistsArrestinsbeta-Arrestin 2beta-ArrestinsCell MovementGreen Fluorescent ProteinsHeLa CellsHumansI-kappa B KinaseIndansLuciferasesMatrix Metalloproteinase 9NF-kappa BProtein Interaction MappingProtein TransportADRB2 protein, humanAdrenergic beta-2 Receptor AgonistsARRB2 protein, humanArrestinsbeta-Arrestin 2beta-ArrestinsGreen Fluorescent ProteinsI-kappa B KinaseindacaterolIndansLuciferasesMatrix Metalloproteinase 9NF-kappa BQuinolonesReceptors, Adrenergic, beta-2Recombinant Fusion ProteinsADRB2indacaterolinvasionMMP-9NF-κB

Identifiers

PMID25134539
PMCPMC4145369
OpenAlexW2091092534

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.