Evidence map›Paper›PMID 25482372›Full record

ArticleEpigenetics2014

Methylation status of IGFBP-3 as a useful clinical tool for deciding on a concomitant radiotherapy.

Olga Pernía, Cristobal Belda-Iniesta, Veronica Pulido, María Cortes-Sempere, Carlos Rodriguez, Olga Vera, Javier Soto, Julia Jiménez, Alvaro Taus, Federico Rojo and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Epigenetics, 2014. 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
0.6field-weighted citation impact, top 31% 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, 20 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. [Research Progress of DNA Methylation in Cisplatin Resistance in Lung Cancer].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2023
    Review
  5. Review
  6. Article
  7. Precision radiotherapy for non-small cell lung cancer.Journal of biomedical science · 2020
    Review
  8. Review
  9. Article
  10. Impact of IGF-1, IGF-1R, and IGFBP-3 promoter methylation on the risk and prognosis of esophageal carcinoma.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
  11. 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

17 authors at 7 institutions in 2 countries.

Olga Perníaa Cancer Epigenetics Laboratory, INGEMM ; University Hospital La Paz ; Madrid , Spain.
Cristobal Belda-Iniesta
Veronica Pulido
María Cortes-Sempere
Carlos Rodriguez
Olga Vera
Javier Soto
Julia Jiménez
Alvaro Taus
Federico Rojo
Edurne Arriola
Ana Rovira
Joan Albanell
M Teresa Macías
Javier de Castro
Rosario Perona
Inmaculada Ibañez de Caceres
Hospital La Paz Institute for Health Research · ESEpigenomics (Germany) · DEMunicipal Institute for Medical Research · ESCentre for Biomedical Network Research on Rare Diseases · ESHospital Del Mar · ESHospital Universitario Fundación Jiménez Díaz · ESHospital Universitario La Paz · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The methylation status of the IGFBP-3 gene is strongly associated with cisplatin sensitivity in patients with non-small cell lung cancer (NSCLC). In this study, we found in vitro evidence that linked the presence of an unmethylated promoter with poor response to radiation. Our data also indicate that radiation might sensitize chemotherapy-resistant cells by reactivating IGFBP-3-expression through promoter demethylation, inactivating the PI3K/AKT pathway. We also explored the IGFBP-3 methylation effect on overall survival (OS) in a population of 40 NSCLC patients who received adjuvant therapy after R0 surgery. Our results indicate that patients harboring an unmethylated promoter could benefit more from a chemotherapy schedule alone than from a multimodality therapy involving radiotherapy and platinum-based treatments, increasing their OS by 2.5 y (p = .03). Our findings discard this epi-marker as a prognostic factor in a patient population without adjuvant therapy, indicating that radiotherapy does not improve survival for patients harboring an unmethylated IGFBP-3 promoter.

Indexed as

Promoter Regions, GeneticAgedAntineoplastic Combined Chemotherapy ProtocolsBiomarkers, TumorCarcinoma, Non-Small-Cell LungCell Line, TumorCell SurvivalCombined Modality TherapyDNA MethylationFemaleHumansInsulin-Like Growth Factor Binding Protein 3Lung NeoplasmsMaleMiddle AgedPhosphorylationBiomarkers, TumorIGFBP3 protein, humanInsulin-Like Growth Factor Binding Protein 3Proto-Oncogene Proteins c-aktATCC, American Type Culture CollectionBS, bisulfite sequencingCDDP cisplatinECACC, European Collection of Cell CultureshypermethylationIGFBP-3IGFBP-3, insulin-like growth factor binding protein-3IGFIR/AKTIR, Ionizing radiationNSCLCNSCLC, non-small cell lung cancerOS, overall survivalqMSP, quantitative methylation specific PCRradiotherapy

Identifiers

PMID25482372
PMCPMC4622698
OpenAlexW2072170172

What OpenQuestion holds

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LicenceCC BY-NC
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.