Evidence map›Paper›PMID 32184357›Full record

ArticleThe Journal of biological chemistry2020

The mRNA levels of heat shock factor 1 are regulated by thermogenic signals via the cAMP-dependent transcription factor ATF3.

Narendra Verma, Luce Perie, Elisabetta Mueller

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

10 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
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  3. Thermogenic Adipose ADH5 Counteracts Age-related Metabolic Decline.bioRxiv : the preprint server for biology · 2025
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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

3 authors at 1 institution in 1 country.

Narendra VermaDivision of Endocrinology, Diabetes and Metabolism, Department of Medicine, New York University, New York, New York 10016.
Luce PerieDivision of Endocrinology, Diabetes and Metabolism, Department of Medicine, New York University, New York, New York 10016.
Elisabetta MuellerDivision of Endocrinology, Diabetes and Metabolism, Department of Medicine, New York University, New York, New York 10016. Electronic address: Elisabetta.Mueller@nyumc.org.
New York University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Heat shock factor 1 (HSF1) regulates cellular adaptation to challenges such as heat shock and oxidative and proteotoxic stresses. We have recently reported a previously unappreciated role for HSF1 in the regulation of energy metabolism in fat tissues; however, whether HSF1 is differentially expressed in adipose depots and how its levels are regulated in fat tissues remain unclear. Here, we show that HSF1 levels are higher in brown and subcutaneous fat tissues than in those in the visceral depot and that HSF1 is more abundant in differentiated, thermogenic adipocytes. Gene expression experiments indicated that HSF1 is transcriptionally regulated in fat by agents that modulate cAMP levels, by cold exposure, and by pharmacological stimulation of β-adrenergic signaling. An

Indexed as

Signal TransductionThermogenesisActivating Transcription Factor 3AdipocytesAnimalsCyclic AMPFemaleHeat-Shock ResponseHeat Shock Transcription FactorsHEK293 CellsHumansMaleMicePromoter Regions, GeneticRNA, MessengerActivating Transcription Factor 3ATF3 protein, humanCyclic AMPHeat Shock Transcription FactorsHsf1 protein, mouseRNA, Messengeractivating transcription factor 3 (ATF3)beta-adrenergic stimulibrown fat/beige fatgene regulationHeat shock factor protein 1 (HSF1)lipid metabolismobesitythermogenesisuncoupling proteinuncoupling protein 1 (UCP1)

Identifiers

PMID32184357
PMCPMC7196654
OpenAlexW3011850089

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.