Evidence map›Paper›PMID 37026525›Full record

ArticleOncology reports2023

NCoA3 upregulation in breast cancer‑associated adipocytes elicits an inflammatory profile.

María Cecilia Lira, Francisco D Rosa, Ignacio Aiello, Mileni Soares Machado, Alejandra G Palma, Leonardo Paz, María Cecilia Salazar Güemes, Silvia Burlando, Pablo J Azurmendi, Natalia Paladino and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Oncology reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
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

12 authors at 2 institutions in 1 country.

María Cecilia LiraInstitute of Medical Research Alfredo Lanari, School of Medicine, University of Buenos Aires, Ciudad Autónoma de Buenos Aires 1427, Argentina.
Francisco D RosaInstitute of Medical Research Alfredo Lanari, School of Medicine, University of Buenos Aires, Ciudad Autónoma de Buenos Aires 1427, Argentina.
Ignacio AielloLaboratory of Chronobiology, National University of Quilmes, Quilmes, Buenos Aires 1876, Argentina.
Mileni Soares MachadoInstitute of Medical Research Alfredo Lanari, School of Medicine, University of Buenos Aires, Ciudad Autónoma de Buenos Aires 1427, Argentina.
Alejandra G PalmaInstitute of Medical Research Alfredo Lanari, School of Medicine, University of Buenos Aires, Ciudad Autónoma de Buenos Aires 1427, Argentina.
Leonardo PazInstitute of Medical Research Alfredo Lanari, School of Medicine, University of Buenos Aires, Ciudad Autónoma de Buenos Aires 1427, Argentina.
María Cecilia Salazar GüemesInstitute of Medical Research Alfredo Lanari, School of Medicine, University of Buenos Aires, Ciudad Autónoma de Buenos Aires 1427, Argentina.
Silvia BurlandoInstitute of Medical Research Alfredo Lanari, School of Medicine, University of Buenos Aires, Ciudad Autónoma de Buenos Aires 1427, Argentina.
Pablo J AzurmendiInstitute of Medical Research Alfredo Lanari, School of Medicine, University of Buenos Aires, Ciudad Autónoma de Buenos Aires 1427, Argentina.
Natalia PaladinoLaboratory of Chronobiology, National University of Quilmes, Quilmes, Buenos Aires 1876, Argentina.
Mónica A CostasInstitute of Medical Research Alfredo Lanari, School of Medicine, University of Buenos Aires, Ciudad Autónoma de Buenos Aires 1427, Argentina.
María Fernanda RubioInstitute of Medical Research Alfredo Lanari, School of Medicine, University of Buenos Aires, Ciudad Autónoma de Buenos Aires 1427, Argentina.
University of Buenos Aires · ARNational University of Quilmes · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nuclear receptor coactivator 3 (NCoA3) is a transcriptional coactivator of NF‑κB and other factors, which is expressed at relatively low levels in normal cells and is amplified or overexpressed in several types of cancer, including breast tumors. NCoA3 levels have been shown to be decreased during adipogenesis; however, its role in tumor‑surrounding adipose tissue (AT) remains unknown. Therefore, the present study assessed the modulation of NCoA3 in breast cancer‑associated adipocytes and evaluated its association with the expression of inflammatory markers. 3T3‑L1 adipocytes were stimulated with conditioned medium from human breast cancer cell lines and the expression levels of NCoA3 were evaluated by reverse transcription‑quantitative (q)PCR. NF‑κB activation was measured by immunofluorescence, and tumor necrosis factor and monocyte chemoattractant protein 1 levels were analyzed by qPCR and dot blot assays. The results obtained from the

Indexed as

Breast NeoplasmsNuclear Receptor Coactivator 33T3-L1 CellsAdipocytesAnimalsFemaleHumansMiceNF-kappa BUp-RegulationNCOA3 protein, humanNcoa3 protein, mouseNF-kappa BNuclear Receptor Coactivator 3breast cancerinflammationmammary adipose tissueNF‑κBnuclear receptor coactivator 3

Identifiers

PMID37026525
PMCPMC10091077
OpenAlexW4362581576

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.