Evidence map›Paper›PMID 25526434›Full record

ArticleMedicine2014

PROX1 gene is differentially expressed in oral cancer and reduces cellular proliferation.

Maria F S D Rodrigues, Camila de Oliveira Rodini, Flávia C de Aquino Xavier, Katiúcia B Paiva, Patrícia Severino, Raquel A Moyses, Rossana M López, Rafael DeCicco, Lília A Rocha, Marcos B Carvalho and 2 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in Medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

19 citing papers in PubMed, 27 citations in OpenAlex.

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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.

Maria F S D RodriguesFrom the Department of Estomatology (MFSDR, LAR, FDN), School of Dentistry; Department of Biochemistry (KBP), Chemistry Institute; Department of Head and Neck Surgery (RAM), School of Medicine; Department of Epidemiology (RML), Public Health; Department of Genetics and Evolutionary Biology (EHT), Institute of Biosciences, University of São Paulo; Albert Einstein Research and Education Institute (PS), Albert Einstein Israelita Hospital, Center for Experimental Research; Department of Head and Neck Surgery (RDC), Arnaldo Vieira de Carvalho Cancer Institute; Department of Head and Neck Surgery (MBC), Heliopolis Hospital Complex, São Paulo; Department of Estomatology (FCdAX), School of Dentistry, Federal University of Bahia, Salvador; Department of Histology (CdOR), School of Dentistry, University of São Paulo, Bauru; and Department of Molecular Biology (EHT), School of Medicine, São José do Rio Preto, Brazil.
Camila de Oliveira Rodini
Flávia C de Aquino Xavier
Katiúcia B Paiva
Patrícia Severino
Raquel A Moyses
Rossana M López
Rafael DeCicco
Lília A Rocha
Marcos B Carvalho
Eloiza H Tajara
Fabio D Nunes
University of Dental Medicine · MMHospital Israelita Albert Einstein · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Homeobox genes are a family of transcription factors that play a pivotal role in embryogenesis. Prospero homeobox 1 (PROX1) has been shown to function as a tumor suppressor gene or oncogene in various types of cancer, including oral squamous cell carcinoma (OSCC). We have previously identified PROX1 as a downregulated gene in OSCC. The aim of this study is to clarify the underlying mechanism by which PROX1 regulates tumorigenicity of OSCC cells. PROX1 mRNA and protein expression levels were first investigated in 40 samples of OSCC and in nontumor margins. Methylation and amplification analysis was also performed to assess the epigenetic and genetic mechanisms involved in controlling PROX1 expression. OSCC cell line SCC9 was also transfected to stably express the PROX1 gene. Next, SCC9-PROX1-overexpressing cells and controls were subjected to proliferation, differentiation, apoptosis, migration, and invasion assays in vitro. OSCC samples showed reduced PROX1 expression levels compared with nontumor margins. PROX1 amplification was associated with better overall survival. PROX1 overexpression reduces cell proliferation and downregulates cyclin D1. PROX1-overexpressing cells also exhibited reduced CK18 and CK19 expression and transcriptionally altered the expression of WISP3, GATA3, NOTCH1, and E2F1. Our results suggest that PROX1 functions as a tumor suppressor gene in oral carcinogenesis.

Indexed as

Gene Expression Regulation, NeoplasticAdultApoptosisBlotting, WesternCell ProliferationFlow CytometryHomeodomain ProteinsHumansImmunohistochemistryMaleMiddle AgedMouth MucosaMouth NeoplasmsProspero-Related Homeobox 1 ProteinReal-Time Polymerase Chain ReactionRNA, NeoplasmHomeodomain ProteinsProspero-Related Homeobox 1 ProteinRNA, NeoplasmTumor Suppressor Proteins

Identifiers

PMID25526434
PMCPMC4603077
OpenAlexW2052220635

What OpenQuestion holds

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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 OpenQuestion graph.