Evidence map›Paper›PMID 33714987›Full record

ArticleOncogene2021

POU1F1 transcription factor induces metabolic reprogramming and breast cancer progression via LDHA regulation.

Anxo Martínez-Ordoñez, Samuel Seoane, Leandro Avila, Noemi Eiro, Manuel Macía, Efigenia Arias, Fabio Pereira, Tomas García-Caballero, Noemi Gómez-Lado, Pablo Aguiar and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Oncogene, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.8field-weighted citation impact, top 5% 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

32 citing papers in PubMed, 55 citations in OpenAlex.

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  19. Transcription factors in fibroblast plasticity and CAF heterogeneity.Journal of experimental & clinical cancer research : CR · 2023
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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

12 authors at 2 institutions in 2 countries.

Anxo Martínez-OrdoñezDepartment of Physiology-Center for Research in Molecular Medicine and Chronic Diseases (CIMUS), University of Santiago de Compostela, Santiago de Compostela, Spain.
Samuel SeoaneDepartment of Physiology-Center for Research in Molecular Medicine and Chronic Diseases (CIMUS), University of Santiago de Compostela, Santiago de Compostela, Spain.
Leandro AvilaDepartment of Physiology-Center for Research in Molecular Medicine and Chronic Diseases (CIMUS), University of Santiago de Compostela, Santiago de Compostela, Spain.
Noemi EiroResearch Unit, Hospital Fundación de Jove, Gijón, Spain.
Manuel MacíaDepartment of Obstetrics and Gynecology, Health Research Institute of Santiago de Compostela (IDIS)-University of Santiago de Compostela, Santiago de Compostela, Spain.
Efigenia AriasDepartment of Obstetrics and Gynecology, Health Research Institute of Santiago de Compostela (IDIS)-University of Santiago de Compostela, Santiago de Compostela, Spain.
Fabio PereiraDepartment of Radiation Oncology, Health Research Institute of Santiago de Compostela (IDIS)-University of Santiago de Compostela, Santiago de Compostela, Spain.
Tomas García-CaballeroDepartment of Morphological Sciences, Health Research Institute of Santiago de Compostela (IDIS)-University of Santiago de Compostela, Santiago de Compostela, Spain.
Noemi Gómez-LadoMolecular Imaging Group. Department of Psychiatry, Radiology, Public Health, Nursing and Medicine, and Health Research Institute of Santiago de Compostela (IDIS). University of Santiago de Compostela, Santiago de Compostela, Spain.
Pablo AguiarMolecular Imaging Group. Department of Psychiatry, Radiology, Public Health, Nursing and Medicine, and Health Research Institute of Santiago de Compostela (IDIS). University of Santiago de Compostela, Santiago de Compostela, Spain.
Francisco VizosoResearch Unit, Hospital Fundación de Jove, Gijón, Spain.
Román Perez-FernandezDepartment of Physiology-Center for Research in Molecular Medicine and Chronic Diseases (CIMUS), University of Santiago de Compostela, Santiago de Compostela, Spain. roman.perez.fernandez@usc.es.ORCID http://orcid.org/0000-0002-5894-0615
Universidade de Santiago de Compostela · ESFundación Hospital de Jove · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metabolic reprogramming is considered hallmarks of cancer. Aerobic glycolysis in tumors cells has been well-known for almost a century, but specific factors that regulate lactate generation and the effects of lactate in both cancer cells and stroma are not yet well understood. In the present study using breast cancer cell lines, human primary cultures of breast tumors, and immune deficient murine models, we demonstrate that the POU1F1 transcription factor is functionally and clinically related to both metabolic reprogramming in breast cancer cells and fibroblasts activation. Mechanistically, we demonstrate that POU1F1 transcriptionally regulates the lactate dehydrogenase A (LDHA) gene. LDHA catalyzes pyruvate into lactate instead of leading into the tricarboxylic acid cycle. Lactate increases breast cancer cell proliferation, migration, and invasion. In addition, it activates normal-associated fibroblasts (NAFs) into cancer-associated fibroblasts (CAFs). Conversely, LDHA knockdown in breast cancer cells that overexpress POU1F1 decreases tumor volume and [

Indexed as

AnimalsCellular ReprogrammingDisease ProgressionHeterograftsHumansL-Lactate DehydrogenaseMCF-7 CellsMiceMice, Inbred BALB CMice, NudeTranscription Factor Pit-1TransfectionLDHA protein, humanL-Lactate DehydrogenasePOU1F1 protein, humanTranscription Factor Pit-1

Identifiers

PMID33714987
PMCPMC8049871
OpenAlexW3137115587

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.