Evidence map›Paper›PMID 28411557›Full record

ReviewRedox biology2017

Controversy about pharmacological modulation of Nrf2 for cancer therapy.

Lidija Milkovic, Neven Zarkovic, Luciano Saso

Open access · goldAbstract readReview
In one paragraph

Review in Redox biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed, 1 pooled it
7.7field-weighted citation impact, top 2% 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

80 citing papers in PubMed, 1 synthesis or guideline pooled it, 140 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
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  5. Article
  6. Review
  7. Review
  8. Article
  9. Antioxidants: a comprehensive review.Archives of toxicology · 2025
    Review
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  11. Review
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  18. Expected and Unexpected Effects of Pharmacological Antioxidants.International journal of molecular sciences · 2023
    Review
  19. Review
  20. Article

20 more citing papers are in PubMed but not listed here.

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

3 authors at 2 institutions in 2 countries.

Lidija MilkovicLaboratory for Oxidative Stress, LabOS, Rudjer Boskovic Institute, Bijenicka 54, HR-10000 Zagreb, Croatia. Electronic address: lidija.milkovic@irb.hr.
Neven ZarkovicLaboratory for Oxidative Stress, LabOS, Rudjer Boskovic Institute, Bijenicka 54, HR-10000 Zagreb, Croatia. Electronic address: zarkovic@irb.hr.
Luciano SasoDepartment of Physiology and Pharmacology "Vittorio Erspamer", Sapienza University of Rome, Piazzale Aldo Moro 5, 00185 Rome, Italy. Electronic address: luciano.saso@uniroma1.it.
Rudjer Boskovic Institute · HRSapienza University of Rome · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Conventional anticancer therapies such as radiotherapy and chemotherapies are associated with oxidative stress generating reactive oxygen species (ROS) and reactive aldehydes like 4-hydroxynonenal in cancer cells that govern them to die. The main mechanism activated due to exposure of the cell to these reactive species is the Nrf2-Keap1 pathway. Although Nrf2 was firstly perceived as a tumor suppressor that inhibits tumor initiation and cancer metastasis, more recent data reveal its role also as a pro-oncogenic factor. Discovery of the upregulation of Nrf2 in different types of cancer supports such undesirable pathophysiological roles of Nrf2. The upregulation of Nrf2 leads to activation of cytoprotective genes thus helping malignant cells to withstand high levels of ROS and to avoid apoptosis, eventually becoming resistant to conventional anticancer therapy. Therefore, new treatment strategies are needed for eradication of cancer and in this review, we will explore two opposing approaches for modulation of Nrf2 in cancer treatments.

Indexed as

AnimalsAntineoplastic AgentsGene Expression Regulation, NeoplasticHumansKelch-Like ECH-Associated Protein 1Molecular Targeted TherapyNeoplasmsNF-E2-Related Factor 2Reactive Oxygen SpeciesSignal TransductionUp-RegulationAntineoplastic AgentsKEAP1 protein, humanKelch-Like ECH-Associated Protein 1NFE2L2 protein, humanNF-E2-Related Factor 2Reactive Oxygen Species4-hydroxynonenalCancerCancer therapyGrowth regulationNrf2Oxidative stress

Identifiers

PMID28411557
PMCPMC5393166
OpenAlexW2604612121

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.