Evidence map›Paper›PMID 38656405›Full record

ArticleThe Journal of cell biology2024

Transcription factor Nrf1 regulates proteotoxic stress-induced autophagy.

Madison A Ward, Janakiram R Vangala, Hatem Elif Kamber Kaya, Holly A Byers, Nayyerehalsadat Hosseini, Antonio Diaz, Ana Maria Cuervo, Susmita Kaushik, Senthil K Radhakrishnan

Open access · hybridAbstract read
In one paragraph

Article in The Journal of cell biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

14 citing papers in PubMed, 15 citations in OpenAlex.

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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

9 authors at 2 institutions in 1 country.

Madison A Ward *Department of Pathology, Virginia Commonwealth University, Richmond, VA, USA.ORCID 0009-0002-5389-9702
Janakiram R Vangala *Department of Pathology, Virginia Commonwealth University, Richmond, VA, USA.ORCID 0000-0001-8494-8461
Hatem Elif Kamber Kaya *Department of Pathology, Virginia Commonwealth University, Richmond, VA, USA.ORCID 0000-0002-2366-9837
Holly A ByersDepartment of Pathology, Virginia Commonwealth University, Richmond, VA, USA.ORCID 0000-0003-4975-3364
Nayyerehalsadat HosseiniDepartment of Pathology, Virginia Commonwealth University, Richmond, VA, USA.ORCID 0000-0003-0443-9371
Antonio DiazDepartment of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, NY, USA.ORCID 0000-0001-7871-0828
Ana Maria CuervoDepartment of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, NY, USA.ORCID 0000-0002-0771-700X
Susmita KaushikDepartment of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, NY, USA.ORCID 0000-0002-6096-5387
Senthil K RadhakrishnanDepartment of Pathology, Virginia Commonwealth University, Richmond, VA, USA.ORCID 0000-0002-5211-9498
Virginia Commonwealth University · USAlbert Einstein College of Medicine · US

Funding

Virus Vector Shared ResourceP30CA016059 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI Kim Felder Rhoads · 1985 to 2026
$51.0M
Nrf1-dependent Proteotoxic Stress Response - Diversity SupplementR01GM132396 · NIGMS · VIRGINIA COMMONWEALTH UNIVERSITY · PI RADHAKRISHNAN, SENTHIL KUMAR · 2019 to 2023
$1.9M
Integrative Training Program in Cancer BiologyT32CA272382 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI Paula Daniela Bos · 2023 to 2026
$1.3M
NCI NIH HHS P30 CA016059NCI NIH HHS T32 CA272382NIGMS NIH HHS R01 GM132396NIH HHS R01GM132396
6 · The paper itself

Abstract

Cells exposed to proteotoxic stress invoke adaptive responses aimed at restoring proteostasis. Our previous studies have established a firm role for the transcription factor Nuclear factor-erythroid derived-2-related factor-1 (Nrf1) in responding to proteotoxic stress elicited by inhibition of cellular proteasome. Following proteasome inhibition, Nrf1 mediates new proteasome synthesis, thus enabling the cells to mitigate the proteotoxic stress. Here, we report that under similar circumstances, multiple components of the autophagy-lysosomal pathway (ALP) were transcriptionally upregulated in an Nrf1-dependent fashion, thus providing the cells with an additional route to cope with proteasome insufficiency. In response to proteasome inhibitors, Nrf1-deficient cells displayed profound defects in invoking autophagy and clearance of aggresomes. This phenomenon was also recapitulated in NGLY1 knockout cells, where Nrf1 is known to be non-functional. Conversely, overexpression of Nrf1 induced ALP genes and endowed the cells with an increased capacity to clear aggresomes. Overall, our results significantly expand the role of Nrf1 in shaping the cellular response to proteotoxic stress.

Indexed as

AutophagyNF-E2-Related Factor 1Proteotoxic StressAnimalsHumansLysosomesMiceNuclear Respiratory Factor 1Proteasome Endopeptidase ComplexProteasome InhibitorsProteostasisStress, PhysiologicalNfe2L1 protein, mouseNF-E2-Related Factor 1NRF1 protein, humanNuclear Respiratory Factor 1Proteasome Endopeptidase ComplexProteasome Inhibitors

Identifiers

PMID38656405
PMCPMC11040505
OpenAlexW4395063844

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.