Evidence map›Paper›PMID 28767070›Full record

ArticleInternational journal of molecular sciences2017

Various Mechanisms Involve the Nuclear Factor (Erythroid-Derived 2)-Like (NRF2) to Achieve Cytoprotection in Long-Term Cisplatin-Treated Urothelial Carcinoma Cell Lines.

Margaretha A Skowron, Günter Niegisch, Philipp Albrecht, Gommert van Koeveringe, Andrea Romano, Peter Albers, Wolfgang A Schulz, Michèle J Hoffmann

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.6field-weighted citation impact, top 34% 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, 14 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Epigenetic Priming and Development of New Combination Therapy Approaches.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
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  8. Article
  9. Stimulated upregulation ofOncology letters · 2019
    Article
  10. Review
  11. Article
  12. 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 2 countries.

Margaretha A SkowronDepartment of Urology, Medical Faculty, Heinrich-Heine-University, Duesseldorf 40225, Germany. Margaretha.Skowron@hhu.de.
Günter NiegischDepartment of Urology, Medical Faculty, Heinrich-Heine-University, Duesseldorf 40225, Germany. Guenter.Niegisch@hhu.de.
Philipp AlbrechtDepartment of Neurology, Medical Faculty, Heinrich-Heine-University, Duesseldorf 40225, Germany. phil.albrecht@gmail.com.
Gommert van KoeveringeDepartment of Urology, Maastricht University Medical Centre, Maastricht 6202AZ, The Netherlands. g.van.koeveringe@mumc.nl.
Andrea RomanoDepartment of Obstetrics and Gynaecology, GROW-School for Oncology & Developmental Biology, Maastricht University Medical Centre, Maastricht 6229HX, The Netherlands. a.romano@maastrichtuniversity.nl.
Peter AlbersDepartment of Urology, Medical Faculty, Heinrich-Heine-University, Duesseldorf 40225, Germany. peter.albers@med.uni-duesseldorf.de.
Wolfgang A SchulzDepartment of Urology, Medical Faculty, Heinrich-Heine-University, Duesseldorf 40225, Germany. Wolfgang.Schulz@hhu.de.
Michèle J HoffmannDepartment of Urology, Medical Faculty, Heinrich-Heine-University, Duesseldorf 40225, Germany. Michele.Hoffmann@hhu.de.
Heinrich Heine University Düsseldorf · DEMaastricht University Medical Centre · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Therapeutic efficacy of cisplatin-based chemotherapy for advanced-stage urothelial carcinoma (UC) is limited by drug resistance. The nuclear factor (erythroid-derived 2)-like 2 (NRF2) pathway is a major regulator of cytoprotective responses. We investigated its involvement in cisplatin resistance in long-term cisplatin treated UC cell lines (LTTs). Expression of NRF2 pathway components and targets was evaluated by qRT-PCR and western blotting in LTT sublines from four different parental cells. NRF2 transcriptional activity was determined by reporter assays and total glutathione (GSH) was quantified enzymatically. Effects of siRNA-mediated NRF2 knockdown on chemosensitivity were analysed by viability assays, γH2AX immunofluorescence, and flow cytometry. Increased expression of NRF2, its positive regulator p62/SQSTM1, and elevated NRF2 activity was observed in 3/4 LTTs, which correlated with KEAP1 expression. Expression of cytoprotective enzymes and GSH concentration were upregulated in some LTTs. NRF2 knockdown resulted in downregulation of cytoprotective enzymes and resensitised 3/4 LTTs towards cisplatin as demonstrated by reduced IC

Indexed as

Cell Line, TumorCisplatinCytoprotectionDrug Resistance, NeoplasmHumansNeoplasm ProteinsNF-E2-Related Factor 2Urinary Bladder NeoplasmsUrotheliumCisplatinNeoplasm ProteinsNFE2L2 protein, humanNF-E2-Related Factor 2cisplatin resistancecytoprotectionglutathionehippo pathwayKelch-like ECH-associated protein 1 (KEAP1)nuclear factor (erythroid-derived 2)-like 2 (NRF2)nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) pathwaysequestosome 1 (p62/SQSTM1)urothelial carcinoma (UC)

Identifiers

PMID28767070
PMCPMC5578070
OpenAlexW2740143797

What OpenQuestion holds

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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.