NRF2 and Primary Cilia: An Emerging Partnership.

NRF2 autophagy cancer ciliogenesis ciliopathy hedgehog signaling mTOR non-small cell lung cancer (NSCLC) primary cilia

Journal

Antioxidants (Basel, Switzerland)
ISSN: 2076-3921
Titre abrégé: Antioxidants (Basel)
Pays: Switzerland
ID NLM: 101668981

Informations de publication

Date de publication:
02 Jun 2020
Historique:
received: 30 04 2020
revised: 30 05 2020
accepted: 31 05 2020
entrez: 6 6 2020
pubmed: 6 6 2020
medline: 6 6 2020
Statut: epublish

Résumé

When not dividing, many cell types target their centrosome to the plasma membrane, where it nucleates assembly of a primary cilium, an antenna-like signaling structure consisting of nine concentric microtubule pairs surrounded by membrane. Primary cilia play important pathophysiological roles in many tissues, their dysfunction being associated with cancer and ciliopathies, a diverse group of congenital human diseases. Several recent studies have unveiled functional connections between primary cilia and NRF2 (nuclear factor erythroid 2-related factor 2), the master transcription factor orchestrating cytoprotective responses to oxidative and other cellular stresses. These NRF2-cilia relationships are reciprocal: primary cilia, by promoting autophagy, downregulate NRF2 activity. In turn, NRF2 transcriptionally regulates genes involved in ciliogenesis and Hedgehog (Hh) signaling, a cilia-dependent pathway with major roles in embryogenesis, stem cell function and tumorigenesis. Nevertheless, while we found that NRF2 stimulates ciliogenesis and Hh signaling, a more recent study reported that NRF2 negatively affects these processes. Herein, we review the available evidence linking NRF2 to primary cilia, suggest possible explanations to reconcile seemingly contradictory data, and discuss what the emerging interplay between primary cilia and NRF2 may mean for human health and disease.

Identifiants

pubmed: 32498260
pii: antiox9060475
doi: 10.3390/antiox9060475
pmc: PMC7346227
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Subventions

Organisme : Ministerio de Economía y Competitividad, Gobierno de España
ID : SAF2015-66568-R (MINECO/FEDER)
Organisme : Ministerio de Economía y Competitividad, Gobierno de España
ID : RYC2013-14887

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Auteurs

Ana Martin-Hurtado (A)

Instituto de Investigaciones Biomédicas Alberto Sols (IIBM), UAM-CSIC, 28029 Madrid, Spain.
Departamento de Bioquímica, Facultad de Medicina, Universidad Autónoma de Madrid (UAM), 28029 Madrid, Spain.
Instituto de Investigación del Hospital Universitario de La Paz (IdiPAZ), 28047 Madrid, Spain.

Isabel Lastres-Becker (I)

Instituto de Investigaciones Biomédicas Alberto Sols (IIBM), UAM-CSIC, 28029 Madrid, Spain.
Departamento de Bioquímica, Facultad de Medicina, Universidad Autónoma de Madrid (UAM), 28029 Madrid, Spain.
Instituto de Investigación del Hospital Universitario de La Paz (IdiPAZ), 28047 Madrid, Spain.
Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), ISCIII, 28013 Madrid, Spain.

Antonio Cuadrado (A)

Instituto de Investigaciones Biomédicas Alberto Sols (IIBM), UAM-CSIC, 28029 Madrid, Spain.
Departamento de Bioquímica, Facultad de Medicina, Universidad Autónoma de Madrid (UAM), 28029 Madrid, Spain.
Instituto de Investigación del Hospital Universitario de La Paz (IdiPAZ), 28047 Madrid, Spain.
Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), ISCIII, 28013 Madrid, Spain.

Francesc R Garcia-Gonzalo (FR)

Instituto de Investigaciones Biomédicas Alberto Sols (IIBM), UAM-CSIC, 28029 Madrid, Spain.
Departamento de Bioquímica, Facultad de Medicina, Universidad Autónoma de Madrid (UAM), 28029 Madrid, Spain.
Instituto de Investigación del Hospital Universitario de La Paz (IdiPAZ), 28047 Madrid, Spain.

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