Evidence map›Paper›PMID 32988635›Full record

ReviewTrends in genetics : TIG2021

Trash Talk: Mammalian Proteasome Regulation at the Transcriptional Level.

Hatem Elif Kamber Kaya, Senthil K Radhakrishnan

Open access · greenAbstract readReview
In one paragraph

Review in Trends in genetics : TIG, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

16 citing papers in PubMed, 30 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

2 authors at 1 institution in 1 country.

Hatem Elif Kamber KayaDepartment of Pathology, Virginia Commonwealth University, Richmond, VA, USA.
Senthil K RadhakrishnanDepartment of Pathology, Virginia Commonwealth University, Richmond, VA, USA. Electronic address: senthil.radhakrishnan@vcuhealth.org.
Virginia Commonwealth University · US

Funding

Nrf1-dependent Proteotoxic Stress Response - Diversity SupplementR01GM132396 · NIGMS · VIRGINIA COMMONWEALTH UNIVERSITY · PI RADHAKRISHNAN, SENTHIL KUMAR · 2019 to 2023
$1.9M
NIGMS NIH HHS R01 GM132396
6 · The paper itself

Abstract

The key to a healthy mammalian cell lies in properly functioning proteolytic machineries called proteasomes. The proteasomes are multisubunit complexes that catalyze the degradation of unwanted proteins and also control half-lives of key cellular regulatory factors. Aberrant proteasome activity is often associated with human diseases such as cancer and neurodegeneration, and so an in-depth understanding of how it is regulated has implications for potential disease interventions. Transcriptional regulation of the proteasome can dictate its abundance and also influence its function, assembly, and location. This ensures proper proteasomal activity in response to developmental cues and to physiological conditions such as starvation and oxidative stress. In this review, we highlight and discuss the roles of the transcription factors that are involved in the regulation of the mammalian proteasome.

Indexed as

AnimalsHumansMammalsNeoplasmsOxidative StressProteasome Endopeptidase ComplexProteinsProteolysisTranscription FactorsTranscription, GeneticProteasome Endopeptidase ComplexProteinsTranscription Factorsproteasome expressiontranscriptional regulationtranscription factors

Identifiers

PMID32988635
PMCPMC7856062
OpenAlexW3088207188

What OpenQuestion holds

Textmetadata
LicenceTDM
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.