Evidence map›Paper›PMID 36994476›Full record

ReviewMolecules and cells2023

The Multi-Faceted Consequences of NRF2 Activation throughout Carcinogenesis.

Christopher J Occhiuto, Jessica A Moerland, Ana S Leal, Kathleen A Gallo, Karen T Liby

Open access · diamondAbstract readReview
In one paragraph

Review in Molecules and cells, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
5.5field-weighted citation impact, top 4% 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

28 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
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  9. Review
  10. Decoding the NRF2-NOTCH Crosstalk in Lung Cancer-An Update.Antioxidants (Basel, Switzerland) · 2025
    Review
  11. Article
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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

5 authors at 1 institution in 1 country.

Christopher J OcchiutoDepartment of Pharmacology and Toxicology, Michigan State University, East Lansing, MI 48824, USA.ORCID https://orcid.org/0000-0002-2218-4504
Jessica A MoerlandDepartment of Pharmacology and Toxicology, Michigan State University, East Lansing, MI 48824, USA.ORCID https://orcid.org/0000-0002-8085-3470
Ana S LealDepartment of Pharmacology and Toxicology, Michigan State University, East Lansing, MI 48824, USA.ORCID https://orcid.org/0000-0001-6472-2879
Kathleen A GalloDepartment of Physiology, Michigan State University, East Lansing, MI 48824, USA.ORCID https://orcid.org/0000-0002-9194-3498
Karen T LibyDepartment of Pharmacology and Toxicology, Michigan State University, East Lansing, MI 48824, USA.ORCID https://orcid.org/0000-0003-3317-3437
Michigan State University · US

Funding

Integrative Pharmacological Sciences Training Program (IPSTP)T32GM142521 · NIGMS · MICHIGAN STATE UNIVERSITY · PI ANNE M. DORRANCE, Gina Marie Leinninger · 2021 to 2026
$2.4M
Nrf2, immune cells and lung cancerR01CA226690 · NCI · MICHIGAN STATE UNIVERSITY · PI LIBY, KAREN T. · 2019 to 2023
$1.6M
NCI NIH HHS R01 CA226690NIGMS NIH HHS T32 GM142521
6 · The paper itself

Abstract

The oxidative balance of a cell is maintained by the Kelch-like ECH-associated protein 1 (KEAP1)/nuclear factor erythroid 2-related factor 2 (NRF2) pathway. This cytoprotective pathway detoxifies reactive oxygen species and xenobiotics. The role of the KEAP1/NRF2 pathway as pro-tumorigenic or anti-tumorigenic throughout stages of carcinogenesis (including initiation, promotion, progression, and metastasis) is complex. This mini review focuses on key studies describing how the KEAP1/NRF2 pathway affects cancer at different phases. The data compiled suggest that the roles of KEAP1/NRF2 in cancer are highly dependent on context; specifically, the model used (carcinogen-induced vs genetic), the tumor type, and the stage of cancer. Moreover, emerging data suggests that KEAP1/NRF2 is also important for regulating the tumor microenvironment and how its effects are amplified either by epigenetics or in response to co-occurring mutations. Further elucidation of the complexity of this pathway is needed in order to develop novel pharmacological tools and drugs to improve patient outcomes.

Indexed as

NeoplasmsNF-E2-Related Factor 2CarcinogenesisHumansKelch-Like ECH-Associated Protein 1Signal TransductionTumor MicroenvironmentKelch-Like ECH-Associated Protein 1NFE2L2 protein, humanNF-E2-Related Factor 2cancerinitiationmetastasisNRF2promotiontransformation

Identifiers

PMID36994476
PMCPMC10070161
OpenAlexW4361276114

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.