Evidence map›Paper›PMID 30820705›Full record

ArticleClinical and experimental medicine2019

Comparison between clinical significance of serum CXCL-8 and classical tumor markers in oesophageal cancer (OC) patients.

Marta Łukaszewicz-Zając, Sara Pączek, Paweł Muszyński, Mirosław Kozłowski, Barbara Mroczko

Open access · hybridAbstract readEvaluation Study
In one paragraph

Article in Clinical and experimental medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.5field-weighted citation impact, top 16% 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

28 citing papers in PubMed, 31 citations in OpenAlex.

  1. Trial
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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

5 authors at 1 institution in 1 country.

Marta Łukaszewicz-ZającDepartment of Biochemical Diagnostics, Medical University of Białystok, ul. Waszyngtona 15 a, 15-269, Białystok, Poland. marta.lukaszewicz-zajac@umb.edu.pl.ORCID http://orcid.org/0000-0002-0185-7327
Sara PączekDepartment of Biochemical Diagnostics, Medical University of Białystok, ul. Waszyngtona 15 a, 15-269, Białystok, Poland.
Paweł MuszyńskiDepartment of Neurodegeneration Diagnostics, Medical University of Białystok, Białystok, Poland.
Mirosław KozłowskiDepartment of Thoracic Surgery, Medical University of Białystok, Białystok, Poland.
Barbara MroczkoDepartment of Biochemical Diagnostics, Medical University of Białystok, ul. Waszyngtona 15 a, 15-269, Białystok, Poland.
Medical University of Białystok · PL

Funding

Uniwersytet Medyczny w Bialymstoku (N/ST/ZB/17/009/2207)
6 · The paper itself

Abstract

C-X-C motif chemokine 8 (CXCL-8), known as interleukin-8, is a pro-inflammatory cytokine which acts as a chemotactic factor, mainly for leukocytes. CXCL-8 is produced by malignant cells, and therefore it can stimulate the growth and progression of various neoplasms, including oesophageal cancer (OC). The aim of the current study was to measure serum concentrations of chemokine CXCL-8 in OC patients and establish whether this protein might be considered a potential candidate for a tumor marker in the diagnosis and progression of OC. The study included 50 OC subjects (32 patients with squamous cell carcinoma of oesophagus-OSCC, 18 patients with adenocarcinoma-OAC) and 26 healthy volunteers. Serum CXCL-8 concentrations were measured using immunoenzymatic assay (ELISA). CRP levels were determined by immunoturbidimetric method, while classical tumor marker levels were measured using chemiluminescent immunoassay. CXCL-8 concentrations were significantly higher in OC patients compared to healthy controls. We demonstrated significant differences between CXCL-8 concentrations and depth of tumor invasion (T factor) in OC patients and OSCC subgroup. In addition, CXCL-8 levels were found to correlate positively with T factor and CRP concentrations. The diagnostic sensitivity, negative predictive value and the area under ROC curve (AUC) of CXCL-8 were higher than those of classical tumor markers. Our findings suggest the potential usefulness of CXCL-8 in the diagnosis and progression of OC. However, due to the non-specific nature of this chemokine, further research is needed to clarify the usefulness of CXCL-8 as a tumor marker of OC.

Indexed as

AdenocarcinomaAdultAgedAged, 80 and overBiomarkers, TumorCarcinoma, Squamous CellDiagnostic Tests, RoutineEsophageal NeoplasmsFemaleHumansImmunoassayInterleukin-8MaleMiddle AgedPredictive Value of TestsROC CurveBiomarkers, TumorCXCL8 protein, humanInterleukin-8ChemokinesCXCL8OesophagealTumor

Identifiers

PMID30820705
PMCPMC6469833
OpenAlexW2919000860

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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.