Evidence map›Paper›PMID 36430487›Full record

ArticleInternational journal of molecular sciences2022

(-)-Epigallocatechin-3-Gallate Prevents IL-1β-Induced uPAR Expression and Invasiveness via the Suppression of NF-κB and AP-1 in Human Bladder Cancer Cells.

Dhiraj Kumar Sah, Pham Ngoc Khoi, Shinan Li, Archana Arjunan, Jae-Uk Jeong, Young Do Jung

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.0field-weighted citation impact, top 8% 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

14 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Cancer chemoprevention: signaling pathways and strategic approaches.Signal transduction and targeted therapy · 2025
    Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
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  11. Reactive Oxygen Species andAntioxidants (Basel, Switzerland) · 2023
    Review
  12. Review
  13. Review
  14. 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

6 authors at 2 institutions in 2 countries.

Dhiraj Kumar SahDepartment of Biochemistry, Chonnam National University Medical School, Hwasun 58128, Republic of Korea.ORCID 0000-0003-1857-6887
Pham Ngoc KhoiFaculty of Basic Medical Sciences, Pham Ngoc Thach University of Medicine, Ho Chi Minh City 740500, Vietnam.
Shinan LiDepartment of Biochemistry, Chonnam National University Medical School, Hwasun 58128, Republic of Korea.
Archana ArjunanDepartment of Biochemistry, Chonnam National University Medical School, Hwasun 58128, Republic of Korea.ORCID 0000-0001-7947-2614
Jae-Uk JeongDepartment of Radiation Oncology, Chonnam National University Medical School, Hwasun 58128, Republic of Korea.
Young Do JungDepartment of Biochemistry, Chonnam National University Medical School, Hwasun 58128, Republic of Korea.ORCID 0000-0003-1209-6786
Chonnam National University Hwasun Hospital · KRPham Ngoc Thach University of Medicine · VN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

(-)-Epigallocatechin-3-O-gallate (EGCG), a primary green tea polyphenol, has powerful iron scavengers, belongs to the family of flavonoids with antioxidant properties, and can be used to prevent cancer. Urokinase-type plasminogen activator receptors (uPARs) are glycosylphosphatidylinositol (GPI)-anchored cell membrane receptors that have crucial roles in cell invasion and metastasis of several cancers including bladder cancer. The mechanism of action of EGCG on uPAR expression has not been reported clearly yet. In this study, we investigated the effect of EGCG on interleukin (IL)-1β-induced cell invasion and uPAR activity in T24 human bladder cancer cells. Interestingly, nuclear factor (NF)-κB and activator protein (AP)-1 transcription factors were critically required for IL-1β-induced high uPAR expression, and EGCG suppressed the transcriptional activity of both the ERK1/2 and JNK signaling pathways with the AP-1 subunit c-Jun. EGCG blocked the IL-1β-stimulated reactive oxygen species (ROS) production, in turn suppressing NF-κB signaling and anti-invasion effects by inhibiting uPAR expression. These results suggest that EGCG may exert at least part of its anticancer effect by controlling uPAR expression through the suppression of ERK1/2, JNK, AP-1, and NF-κB.

Indexed as

Transcription Factor AP-1Urinary Bladder NeoplasmsCatechinHumansNF-kappa BReceptors, Urokinase Plasminogen ActivatorCatechinepigallocatechin gallateNF-kappa BReceptors, Urokinase Plasminogen ActivatorTranscription Factor AP-1AP-1cell invasionEGCGIL-1βNF-κBROSUrokinase-type plasminogen activator receptor (uPAR)

Identifiers

PMID36430487
PMCPMC9697952
OpenAlexW4309007676

What OpenQuestion holds

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LicenceCC BY
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.