Evidence map›Paper›PMID 31835715›Full record

ArticleAntioxidants (Basel, Switzerland)2019

Chronic Oxidative Stress Promotes Molecular Changes Associated with Epithelial Mesenchymal Transition, NRF2, and Breast Cancer Stem Cell Phenotype.

Ana Čipak Gašparović, Lidija Milković, Nadia Dandachi, Stefanie Stanzer, Iskra Pezdirc, Josip Vrančić, Sanda Šitić, Christoph Suppan, Marija Balic

Open access · goldAbstract read
In one paragraph

Article in Antioxidants (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.9field-weighted citation impact, top 12% 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

20 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
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  6. Review
  7. Plants (Basel, Switzerland) · 2023
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  11. Review
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  15. Article
  16. Elk-1 transcriptionally regulates ZC3H4 expression to promote silica-induced epithelial-mesenchymal transition.Laboratory investigation; a journal of technical methods and pathology · 2020
    Article
  17. Review
  18. Free Radical Research in Cancer.Antioxidants (Basel, Switzerland) · 2020
    Article
  19. Article
  20. 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

9 authors at 4 institutions in 3 countries.

Ana Čipak GašparovićDivision of Molecular Medicine, Ruđer Bošković Institute, HR-10000 Zagreb, Croatia.ORCID 0000-0003-2000-8950
Lidija MilkovićDivision of Molecular Medicine, Ruđer Bošković Institute, HR-10000 Zagreb, Croatia.ORCID 0000-0002-4484-039X
Nadia DandachiDepartment of Internal Medicine, Division of Oncology, Medical University, Graz 8036, Austria.ORCID 0000-0001-9093-0743
Stefanie StanzerDepartment of Internal Medicine, Division of Oncology, Medical University, Graz 8036, Austria.
Iskra PezdircOuthospital Emergency Medicine Department of Krapina Zagorje County, HR-49000 Krapina, Croatia.
Josip VrančićInstitute of Cancer Sciences, University of Glasgow, Glasgow G12 8QQ, UK.
Sanda ŠitićSestre milosrdnice University Hospital Centre, University Hospital for Tumors, HR-10000 Zagreb, Croatia.
Christoph SuppanDepartment of Internal Medicine, Division of Oncology, Medical University, Graz 8036, Austria.
Marija BalicDepartment of Internal Medicine, Division of Oncology, Medical University, Graz 8036, Austria.
Medical University of Graz · ATRuđer Bošković Institute · HRCancer Research UK Scotland Institute · GBUniversity Hospital Centre Zagreb · HR

Funding

Croatian-Austrian bilateral project WTZ HR 01/12OENB No´14001
6 · The paper itself

Abstract

Oxidative stress plays a role in carcinogenesis, but it also contributes to the modulation of tumor cells and microenvironment caused by chemotherapeutics. One of the consequences of oxidative stress is lipid peroxidation, which can, through reactive aldehydes such as 4-hydroxy-2-nonenal (HNE), affect cell signaling pathways. On the other hand, cancer stem cells (CSC) are now recognized as a major factor of malignancy by causing metastasis, relapse, and therapy resistance. Here, we evaluated whether oxidative stress and HNE modulation of the microenvironment can influence CSC growth, modifications of the epithelial to mesenchymal transition (EMT) markers, the antioxidant system, and the frequency of breast cancer stem cells (BCSC). Our results showed that oxidative changes in the microenvironment of BCSC and particularly chronic oxidative stress caused changes in the proliferation and growth of breast cancer cells. In addition, changes associated with EMT, increase in glutathione (GSH) and Nuclear factor erythroid 2-related factor 2 (NRF2) were observed in breast cancer cells grown on HNE pretreated collagen and under chronic oxidative stress. Our results suggest that chronic oxidative stress can be a bidirectional modulator of BCSC fate. Low levels of HNE can increase differentiation markers in BCSC, while higher levels increased GSH and NRF2 as well as certain EMT markers, thereby increasing therapy resistance.

Indexed as

4-hydroxy-2-nonenalbreast cancer stem cellsextracellular matrixNRF2

Identifiers

PMID31835715
PMCPMC6943739
OpenAlexW2996259073

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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.