Evidence map›Paper›PMID 24040446›Full record

ArticleInternational journal of clinical and experimental pathology2013

Cellular retinol binding protein 1 could be a tumor suppressor gene in cervical cancer.

Mónica Mendoza-Rodriguez, Hugo Arreola, Alejandra Valdivia, Raúl Peralta, Humberto Serna, Vanessa Villegas, Pablo Romero, Beatriz Alvarado-Hernández, Lucero Paniagua, Daniel Marrero-Rodríguez and 2 more

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

11 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Coronary artery disease-associated immune geneFrontiers in cardiovascular medicine · 2023
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  8. Review
  9. Review
  10. Article
  11. Methylation of PRDM2, PRDM5 and PRDM16 genes in lung cancer cells.International journal of clinical and experimental pathology · 2014
    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 1 institution in 1 country.

Mónica Mendoza-RodriguezLaboratorio de Oncogenómica, Unidad de Investigación Médica en Enfermedades Oncológicas, UMAE Hospital de Oncología CMN SXXI, IMSS Av. Cuauhtémoc 330, Col. Doctores, México D.F. 06720 ; Departamento de Biomedicina Molecular, Centro de Investigación y de Estudios Avanzados IPN, México ; Actual address: AV, Centro Interdisciplinario de Ciencias de la Salud, Unidad Milpa Alta, Instituto Politécnico Nacional Méx.
Hugo Arreola
Alejandra Valdivia
Raúl Peralta
Humberto Serna
Vanessa Villegas
Pablo Romero
Beatriz Alvarado-Hernández
Lucero Paniagua
Daniel Marrero-Rodríguez
Marco A Meraz
Mauricio Salcedo
Instituto Politécnico Nacional · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsCervical Cancer (CC) is one of the most important health problems in women. It frequently presents genetic changes at chromosome region 3q21. This region contains the Cellular Retinol Binding Protein 1 gene (CRBP1) which has been implicated as an important element in the development of other types of cancer. The main goal of the present work was to determine the molecular alterations of CRBP1 and its relationship to CC.

methodsTo determine the molecular alterations of CRBP1 gene in CC; twenty-six CC and twenty-six healthy cervix samples were evaluated for: 1) Copy number gain by real-time PCR analysis, 2) expression levels by an immunohistochemistry assay on tissue microarray, and 3) the methylation status of the CRBP1 promoter region.

resultsThe increase in CRBP1 copy number was observed in 10 out of the 26 CC samples analyzed, while healthy cervices samples showed no changes in the copy number. In addition, there was a lack of expression of the CRBP1 gene in an important number of the CC samples (17/26), and the CRBP1 gene promoter was methylated in 15/26 of the CC samples. Interestingly, there was a significant association between the lack of expression of the CRBP1 gene and its methylation status.

conclusionsThe data indicates that, both activating and inactivating changes in the CRBP1 gene could be significant events in the development and progression of CC, and the lack of expression of the CRBP1 protein could be related with to the development of CC. We believe that there is enough evidence to consider to CRBP1 gene as a tumor suppressor gene for CC.

Indexed as

Genes, Tumor SuppressorBiomarkers, TumorCarcinoma, Squamous CellCase-Control StudiesDNA Copy Number VariationsDNA MethylationFemaleGene DosageGene Expression Regulation, NeoplasticGenetic Predisposition to DiseaseHeLa CellsHumansMiddle AgedPhenotypePromoter Regions, GeneticRetinol-Binding Proteins, CellularBiomarkers, TumorRBP1 protein, humanRetinol-Binding Proteins, CellularCervical cancercopy numberCRBP1expressionsuppressor gene

Identifiers

PMID24040446
PMCPMC3759488
OpenAlexW1522623738

What OpenQuestion holds

Textmetadata
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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.