Evidence map›Paper›PMID 25527274›Full record

ArticleBreast cancer research : BCR2014

Cancer progression by breast tumors with Pit-1-overexpression is blocked by inhibition of metalloproteinase (MMP)-13.

Juan Sendon-Lago, Samuel Seoane, Noemi Eiro, Maria A Bermudez, Manuel Macia, Tomas Garcia-Caballero, Francisco J Vizoso, Roman Perez-Fernandez

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Breast cancer research : BCR, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Juan Sendon-LagoDepartment of Physiology- Center for Research in Molecular Medicine and Chronic Diseases (CIMUS), School of Medicine, University of Santiago de Compostela, Praza do Obradoiro, Santiago de Compostela, 15782, Spain. bautistax@hotmail.com.
Samuel SeoaneDepartment of Physiology- Center for Research in Molecular Medicine and Chronic Diseases (CIMUS), School of Medicine, University of Santiago de Compostela, Praza do Obradoiro, Santiago de Compostela, 15782, Spain. samuel.seoane@usc.es.
Noemi EiroUnidad de Investigación, Fundacion Hospital de Jove, Avenida Eduardo Castro, Gijón, 33290, Spain. investigacion@hospitaldejove.com.
Maria A BermudezDepartment of Physiology- Center for Research in Molecular Medicine and Chronic Diseases (CIMUS), School of Medicine, University of Santiago de Compostela, Praza do Obradoiro, Santiago de Compostela, 15782, Spain. maria.bermudez@usc.es.
Manuel MaciaDepartments of Obstetrics and Gynecology, School of Medicine, University of Santiago de Compostela, Praza do Obradoiro, Santiago de Compostela, 15782, Spain. manuelmaciac@msn.com.
Tomas Garcia-CaballeroDepartments of Morphological Sciences, School of Medicine, University of Santiago de Compostela, Praza do Obradoiro, Santiago de Compostela, 15782, Spain. tomas.garcia-caballero@usc.es.
Francisco J VizosoUnidad de Investigación, Fundacion Hospital de Jove, Avenida Eduardo Castro, Gijón, 33290, Spain. franvizoso@gmail.com.
Roman Perez-FernandezDepartment of Physiology- Center for Research in Molecular Medicine and Chronic Diseases (CIMUS), School of Medicine, University of Santiago de Compostela, Praza do Obradoiro, Santiago de Compostela, 15782, Spain. roman.perez.fernandez@usc.es.
Center for Research in Molecular Medicine and Chronic Diseases · ESFundación Hospital de Jove · ESUniversidade de Santiago de Compostela · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe POU class 1 homeobox 1 transcription factor (POU1F1, also known as Pit-1) is expressed in the mammary gland and its overexpression induces profound phenotypic changes in proteins involved in cell proliferation, apoptosis, and invasion. Patients with breast cancer and elevated expression of Pit-1 show a positive correlation with the occurrence of distant metastasis. In this study we evaluate the relationship between Pit-1 and two collagenases: matrix metalloproteinase-1 (MMP-1) and matrix metalloproteinase-13 (MMP-13), which have been related to metastasis in breast cancer.

methodsWe began by transfecting the MCF-7 and MDA-MB-231 human breast adenocarcinoma cell lines with the Pit-1 overexpression vector (pRSV-hPit-1). Afterward, the mRNA, protein, and transcriptional regulation of both MMP-1 and MMP-13 were evaluated by real-time PCR, Western blot, chromatin immunoprecipitation (ChIP), and luciferase reporter assays. We also evaluated Pit-1 overexpression with MMP-1 and MMP-13 knockdown in a severe combined immunodeficiency (SCID) mouse tumor xenograft model. Finally, by immunohistochemistry we correlated Pit-1 with MMP-1 and MMP-13 protein expression in 110 human breast tumors samples.

resultsOur data show that Pit-1 increases mRNA and protein of both MMP-1 and MMP-13 through direct transcriptional regulation. In SCID mice, knockdown of MMP-13 completely blocked lung metastasis in Pit-1-overexpressing MCF-7 cells injected into the mammary fat pad. In breast cancer patients, expression of Pit-1 was found to be positively correlated with the presence of both MMP-1 and MMP-13.

conclusionsOur data indicates that Pit-1 regulates MMP-1 and MMP-13, and that inhibition of MMP-13 blocked invasiveness to lung in Pit-1-overexpressed breast cancer cells.

Indexed as

Gene Expression Regulation, NeoplasticAdenocarcinomaAnimalsApoptosisBreast NeoplasmsCell Line, TumorCell ProliferationFemaleHumansLung NeoplasmsMatrix Metalloproteinase 1Matrix Metalloproteinase 13MCF-7 CellsMiceNeoplasm InvasivenessNeoplasm MetastasisMatrix Metalloproteinase 1Matrix Metalloproteinase 13MMP13 protein, humanMMP1 protein, humanPOU1F1 protein, humanRNA, MessengerTranscription Factor Pit-1

Identifiers

PMID25527274
PMCPMC4305241
OpenAlexW1975161794

What OpenQuestion holds

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LicenceCC BY
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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.