Evidence map›Paper›PMID 29409457›Full record

ArticleBMC cancer2018

The potential predictive value of DEK expression for neoadjuvant chemoradiotherapy response in locally advanced rectal cancer.

J Martinez-Useros, I Moreno, M J Fernandez-Aceñero, M Rodriguez-Remirez, A Borrero-Palacios, A Cebrian, T Gomez Del Pulgar, L Del Puerto-Nevado, W Li, A Puime-Otin and 3 more

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
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  4. Potential ofMolecular and clinical oncology · 2022
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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

13 authors at 4 institutions in 1 country.

J Martinez-UserosTranslational Oncology Division, OncoHealth Institute, Health Research Institute - University Hospital "Fundación Jiménez Díaz"-UAM, Av. Reyes Católicos 2, 28040, Madrid, Spain. javier.museros@oncohealth.eu.
I MorenoTranslational Oncology Division, OncoHealth Institute, Health Research Institute - University Hospital "Fundación Jiménez Díaz"-UAM, Av. Reyes Católicos 2, 28040, Madrid, Spain.
M J Fernandez-AceñeroDepartment of Pathology, Clinico San Carlos University Hospital, Madrid, Spain.
M Rodriguez-RemirezTranslational Oncology Division, OncoHealth Institute, Health Research Institute - University Hospital "Fundación Jiménez Díaz"-UAM, Av. Reyes Católicos 2, 28040, Madrid, Spain.
A Borrero-PalaciosTranslational Oncology Division, OncoHealth Institute, Health Research Institute - University Hospital "Fundación Jiménez Díaz"-UAM, Av. Reyes Católicos 2, 28040, Madrid, Spain.
A CebrianTranslational Oncology Division, OncoHealth Institute, Health Research Institute - University Hospital "Fundación Jiménez Díaz"-UAM, Av. Reyes Católicos 2, 28040, Madrid, Spain.
T Gomez Del PulgarTranslational Oncology Division, OncoHealth Institute, Health Research Institute - University Hospital "Fundación Jiménez Díaz"-UAM, Av. Reyes Católicos 2, 28040, Madrid, Spain.
L Del Puerto-NevadoTranslational Oncology Division, OncoHealth Institute, Health Research Institute - University Hospital "Fundación Jiménez Díaz"-UAM, Av. Reyes Católicos 2, 28040, Madrid, Spain.
W LiTranslational Oncology Division, OncoHealth Institute, Health Research Institute - University Hospital "Fundación Jiménez Díaz"-UAM, Av. Reyes Católicos 2, 28040, Madrid, Spain.
A Puime-OtinDepartment of Pathology, University Hospital "Fundación Jiménez Díaz"-UAM, Madrid, Spain.
N PerezDepartment of Pathology, University Hospital "Fundación Jiménez Díaz"-UAM, Madrid, Spain.
M S SoengasMelanoma Research Group, Spanish National Cancer Research Centre, Madrid, Spain.
J Garcia-FoncillasTranslational Oncology Division, OncoHealth Institute, Health Research Institute - University Hospital "Fundación Jiménez Díaz"-UAM, Av. Reyes Católicos 2, 28040, Madrid, Spain. jgfoncillas@gmail.com.
Universidad Autónoma de Madrid · ESHospital Universitario Fundación Jiménez Díaz · ESHospital Clínico San Carlos · ESSpanish National Cancer Research Centre · ES

Funding

Instituto de Salud Carlos III-FEDER PI16/01468RNA-Reg CONSOLIDER Network CSD2009-00080
6 · The paper itself

Abstract

backgroundLimited data are available regarding the ability of biomarkers to predict complete pathological response to neoadjuvant chemoradiotherapy in locally advanced rectal cancer. Complete response translates to better patient survival. DEK is a transcription factor involved not only in development and progression of different types of cancer, but is also associated with treatment response. This study aims to analyze the role of DEK in complete pathological response following chemoradiotherapy for locally advanced rectal cancer.

methodsPre-treated tumour samples from 74 locally advanced rectal-cancer patients who received chemoradiation therapy prior to total mesorectal excision were recruited for construction of a tissue microarray. DEK immunoreactivity from all samples was quantified by immunohistochemistry. Then, association between positive stained tumour cells and pathologic response to neoadjuvant treatment was measured to determine optimal predictive power.

resultsDEK expression was limited to tumour cells located in the rectum. Interestingly, high percentage of tumour cells with DEK positiveness was statistically associated with complete pathological response to neoadjuvant treatment based on radiotherapy and fluoropyrimidine-based chemotherapy and a marked trend toward significance between DEK positiveness and absence of treatment toxicity. Further analysis revealed an association between DEK and the pro-apoptotic factor P38 in the pre-treated rectal cancer biopsies.

conclusionsThese data suggest DEK as a potential biomarker of complete pathological response to treatment in locally advanced rectal cancer.

Indexed as

AgedAged, 80 and overBiomarkers, TumorChemoradiotherapyChromosomal Proteins, Non-HistoneFemaleHumansImmunohistochemistryMaleMiddle AgedNeoadjuvant TherapyOncogene ProteinsPoly-ADP-Ribose Binding ProteinsPredictive Value of TestsPrognosisRectal NeoplasmsBiomarkers, TumorChromosomal Proteins, Non-HistoneDEK protein, humanOncogene ProteinsPoly-ADP-Ribose Binding ProteinsChemoradiotherapyComplete pathological responseDEKNeoadjuvant treatmentPredictive biomarkerRectal cancer

Identifiers

PMID29409457
PMCPMC5801838
OpenAlexW2804763998

What OpenQuestion holds

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Registered trials

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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.