Evidence map›Paper›PMID 20974733›Full record

ArticleThe journals of gerontology. Series A, Biological sciences and medical sciences2011

Genetic deletion of Nrf2 promotes immortalization and decreases life span of murine embryonic fibroblasts.

Laura Jódar, Evi M Mercken, Julia Ariza, Caitlin Younts, José A González-Reyes, Francisco J Alcaín, Isabel Burón, Rafael de Cabo, José M Villalba

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The journals of gerontology. Series A, Biological sciences and medical sciences, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

22 citing papers in PubMed, 31 citations in OpenAlex.

  1. Adenosine APharmaceuticals (Basel, Switzerland) · 2026
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  11. Proteome Stability as a Key Factor of Genome Integrity.International journal of molecular sciences · 2017
    Review
  12. Article
  13. Article
  14. DNA Damage: A Main Determinant of Vascular Aging.International journal of molecular sciences · 2016
    Review
  15. The role of transcription factor Nrf2 in skin cells metabolism.Archives of dermatological research · 2015
    Review
  16. Article
  17. Sirtuin activation: a role for plasma membrane in the cell growth puzzle.The journals of gerontology. Series A, Biological sciences and medical sciences · 2013
    Article
  18. Disruption of Nrf2 signaling impairs angiogenic capacity of endothelial cells: implications for microvascular aging.The journals of gerontology. Series A, Biological sciences and medical sciences · 2012
    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 2 institutions in 2 countries.

Laura JódarDepartamento de Biología Celular, Fisiología e Inmunología, Facultad de Ciencias, Universidad de Córdoba, Spain.
Evi M Mercken
Julia Ariza
Caitlin Younts
José A González-Reyes
Francisco J Alcaín
Isabel Burón
Rafael de Cabo
José M Villalba
University of Córdoba · ESNational Institutes of Health · US

Funding

NRF2 interactions with SIRT1 and its role on caloric restrictionZIAAG000361 · NIA · NATIONAL INSTITUTE ON AGING · PI DE CABO, RAFAEL · 2009 to 2024
$5.3M
Aging and CR effects on the Plasma Membrane Redox SystemZIAAG000362 · NIA · NATIONAL INSTITUTE ON AGING · PI DE CABO, RAFAEL · 2009 to 2025
$5.0M
6 · The paper itself

Abstract

Nuclear factor E2-related factor-2 (Nrf2) transcription factor is one of the main regulators of intracellular redox balance and a sensor of oxidative and electrophilic stress. Low Nrf2 activity is usually associated with carcinogenesis, but Nrf2 is also considered as an oncogene because it increases survival of transformed cells. Because intracellular redox balance alterations are involved in both senescence and tumorigenesis, we investigated the impact of Nrf2 genetic deletion on cellular immortalization and life span of murine embryonic fibroblasts. We report that Nrf2 genetic deletion promotes immortalization due to an early loss of p53-dependent gene expression. However, compared with control cells, immortalized Nrf2-/- murine embryonic fibroblasts exhibited decreased growth, lower cyclin E levels, and impaired expression of NQO1 and cytochrome b₅ reductase. Moreover, SirT1 was also significantly reduced in immortalized Nrf2-/- murine embryonic fibroblasts, and these cells exhibited shorter life span. Our results underscore the dual role of Nrf2 in protection against carcinogenesis and in the delay of cellular aging.

Indexed as

Gene Expression RegulationAnimalsCellular SenescenceFibroblastsMiceNF-E2-Related Factor 2Sequence DeletionNF-E2-Related Factor 2

Identifiers

PMID20974733
PMCPMC4007826
OpenAlexW2131611717

What OpenQuestion holds

Textmetadata
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.