Evidence map›Paper›PMID 40317955›Full record

ArticleFEBS letters2025

Spot-14 and its paralog Spot-14R regulate expression of metabolic and thermogenic pathway genes in murine brown and beige adipocytes.

Lidia Itzel Castro-Rodríguez, Cristina Velez-delValle, Claudia Patricia Hernández-Mosqueira, Walid Kuri-Harcuch

Abstract read
In one paragraph

Article in FEBS letters, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Lidia Itzel Castro-RodríguezDepartment of Cell Biology, Center for Research and Advanced Studies (Cinvestav), Mexico City, Mexico.
Cristina Velez-delValleDepartment of Cell Biology, Center for Research and Advanced Studies (Cinvestav), Mexico City, Mexico.
Claudia Patricia Hernández-MosqueiraDepartment of Cell Biology, Center for Research and Advanced Studies (Cinvestav), Mexico City, Mexico.
Walid Kuri-HarcuchDepartment of Cell Biology, Center for Research and Advanced Studies (Cinvestav), Mexico City, Mexico.ORCID https://orcid.org/0000-0001-7278-7568

Funding

Consejo Nacional de Humanidades, Ciencias y Tecnologías 2039
6 · The paper itself

Abstract

Spot 14 (S14), encoded by Thrsp, is a thyroid hormone-responsive transcriptional activator that regulates lipogenesis, though its mechanisms remain unclear. We aimed to study the role of S14 on gene expression in adipocytes. We analyzed Thrsp and its paralog Mid1ip1 in brown (EB5), beige (EB7), and white (F442A) adipocytes. Thrsp expression was higher in EB5 and EB7 than in F442A and increased with thyroid hormone T3 in EB5 and EB7 but decreased in F442A. Mid1ip1 expression rose moderately in EB5 and EB7, influencing lipid metabolism genes. Silencing Thrsp upregulated Mid1ip1 in EB7 and reduced thermogenic gene expression in EB5 and EB7. These findings underscore the roles of Thrsp and Mid1ip1 in metabolic and thermogenic pathways, highlighting the responsiveness of S14 to thyroid hormones and nutrient signals. Impact statement This study reveals that Thyroid Hormone-Induced Protein 8 (THRSP), also known as Spot-14, and its paralog Spot-14R, regulate metabolic and thermogenic gene expression differently in brown and beige adipocytes. These findings provide insights into adipocyte metabolism, offering potential targets for obesity and metabolic disorder treatments.

Indexed as

Adipocytes, BeigeAdipocytes, BrownGene Expression RegulationThermogenesisTranscription FactorsAnimalsLipid MetabolismMiceTranscription Factorsadipocytesbrite/beige adipocytesbrown adipocytesSpot14thermogenesisThsrp

Identifiers

PMID40317955
PMCPMC12183620

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.