Evidence map›Paper›PMID 23029430›Full record

ArticlePloS one2012

Prognostic role of host cyclooxygenase and cytokine genotypes in a Caucasian cohort of patients with gastric adenocarcinoma.

María Asunción García-González, David Nicolás-Pérez, Angel Lanas, Luis Bujanda, Patricia Carrera, Rafael Benito, Mark Strunk, Federico Sopeña, Santos Santolaria, Elena Piazuelo and 13 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 20% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 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

23 authors at 15 institutions in 1 country.

María Asunción García-GonzálezInstituto de Investigación Sanitaria Aragón (IIS Aragón), Zaragoza, Spain. asgarcia@unizar.es
David Nicolás-Pérez
Angel Lanas
Luis Bujanda
Patricia Carrera
Rafael Benito
Mark Strunk
Federico Sopeña
Santos Santolaria
Elena Piazuelo
Pilar Jiménez
Rafael Campo
Jesús Espinel
Marisa Manzano
Fernando Geijo
María Pellisé
Ferrán González-Huix
Jorge Espinós
Manuel Zaballa
Llúcia Titó
Luis Barranco
Roberto Pazo
Enrique Quintero
Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas · ESHospital Universitario de Canarias · ESInstituto de Investigación Sanitaria Aragón · ESDeleted InstitutionHospital Clínic de Barcelona · ESHospital de Cruces · ESHospital de León · ESHospital Del Mar · ESHospital de Mataró · ESHospital General San Jorge · ESHospital Universitari de Girona Doctor Josep Trueta · ESHospital Universitario Miguel Servet · ESResearch Institute Hospital 12 de Octubre · ESUniversidad de Zaragoza · ESUniversity Hospital Mútua de Terrassa · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGenetic factors influencing the prognosis of gastric adenocarcinoma (GAC) are not well known. Given the relevance of cytokines and other pro-inflammatory mediators in cancer progression and invasiveness, we aimed to assess the prognostic role of several functional cytokine and cyclooxygenase gene polymorphisms in patients with GAC. METHODOLOGY: Genomic DNA from 380 Spanish Caucasian patients with primary GAC was genotyped for 23 polymorphisms in pro-inflammatory (IL1B, TNFA, LTA, IL6, IL12p40), anti-inflammatory (IL4, IL1RN, IL10, TGFB1) cytokine, and cyclooxygenase (PTGS1 and PTGS2) genes by PCR, RFLP and TaqMan assays. Clinical and histological information was collected prospectively. Survival curves were estimated by the Kaplan-Meier method and compared using the log rank test. Outcome was determined by analysis of Cox proportional hazards, adjusting for confounding factors.

resultsThe median follow-up period and median overall survival (OS) time were 9.9 months (range 0.4-120.3) and 10.9 months (95% CI: 8.9-14.1), respectively. Multivariate analysis identified tumor stages III (HR, 3.23; 95% CI:2-5.22) and IV (HR, 5.5; 95% CI: 3.51-8.63) as independent factors associated with a significantly reduced OS, whereas surgical treatment (HR: 0.44; 95%CI: 0.3-0.6) was related to a better prognosis of the disease. Concerning genetic factors, none of the 23 polymorphisms evaluated in the current study did influence survival. Moreover, no gene-environment interactions on GAC prognosis were observed.

conclusionsOur results show that, in our population, the panel of selected pro- and anti-inflammatory cytokine, and cyclooxygenase gene polymorphisms are not relevant in determining the prognosis of gastric adenocarcinoma.

Indexed as

White PeopleAdenocarcinomaAgedAged, 80 and overCohort StudiesCyclooxygenase 1Cyclooxygenase 2CytokinesFemaleGene-Environment InteractionGenotypeHumansMaleMiddle AgedNeoplasm StagingPolymorphism, Restriction Fragment LengthCyclooxygenase 1Cyclooxygenase 2CytokinesPTGS1 protein, humanPTGS2 protein, human

Identifiers

PMID23029430
PMCPMC3460851
OpenAlexW1989139331

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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.