Evidence map›Paper›PMID 26818832›Full record

ArticleVirchows Archiv : an international journal of pathology2016

Expression of the CXCR4 ligand SDF-1/CXCL12 is prognostically important for adenocarcinoma and large cell carcinoma of the lung.

William Sterlacci, Shereen Saker, Bettina Huber, Michael Fiegl, Alexandar Tzankov

Abstract read
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In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
1.6field-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

12 citing papers in PubMed, 2 syntheses or guidelines pooled it, 19 citations in OpenAlex.

  1. Pooled it
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  11. Alcohol-Mediated Organ Damages: Heart and Brain.Frontiers in pharmacology · 2018
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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 3 institutions in 3 countries.

William SterlacciInstitute of Pathology, Hospital Bayreuth, Preuschwitzerstrasse 101, Bayreuth, 95445, Germany. william.sterlacci@klinikum-bayreuth.de.
Shereen SakerInstitute of Pathology, Hospital Bayreuth, Preuschwitzerstrasse 101, Bayreuth, 95445, Germany.
Bettina HuberInstitute of Pathology, University Hospital Basel, Schoenbeinstrasse 40, Basel, 4031, Switzerland.
Michael FieglDepartment of Internal Medicine, Oncology and Geriatrics, Hospital Hochrum, Lärchenstrasse 41, Rum bei Innsbruck, 6063, Austria.
Alexandar TzankovInstitute of Pathology, University Hospital Basel, Schoenbeinstrasse 40, Basel, 4031, Switzerland.
Bayreuth Medical Center · DEUniversity Hospital of Basel · CHInnsbruck Medical University · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The SDF-1/CXCR4 axis is associated with tumor progression and has been reported as a prognostic parameter, although with conflicting data for non-small cell lung cancer (NSCLC). This study examines a large cohort of clinically and pathologically well-characterized NSCLC patients and includes the activated form of CXCR4 (pCXCR4), which has not been studied in this context so far. SDF-1, CXCR4, and pCXCR4 were assessed immunohistochemically in 371 surgically resected NSCLC using a standardized tissue microarray platform. Extensive clinical and pathological data and a postoperative follow-up period of 17 years enabled detailed correlations. CXCR4 and pCXCR4 were frequently expressed on squamous cell carcinoma. Membranous expression of SDF-1 was a marker of poor prognosis and proved to be an independent prognostic parameter for the entire cohort and for patients with adenocarcinoma (ACA) and large cell carcinoma (LCC). Targeted cancer therapies blocking SDF-1/CXCR4 interaction already exist, and our data suggest that expression of SDF-1, especially on poorer prognosis subgroups of LCC and ACA, indicates patients that might benefit more than others. This should be taken into account when assessing the effectiveness of such targeted approaches for NSCLC patients and could lead to important implications.

Indexed as

AdenocarcinomaAdenocarcinoma of LungAgedBiomarkers, TumorCarcinoma, Large CellChemokine CXCL12Disease-Free SurvivalFemaleHumansImmunohistochemistryKaplan-Meier EstimateLung NeoplasmsMaleMiddle AgedPrognosisProportional Hazards ModelsBiomarkers, TumorChemokine CXCL12CXCL12 protein, humanCXCR4Non-small cell lung cancerPrognosisSDF-1

Identifiers

PMID26818832
OpenAlexW2253193571

What OpenQuestion holds

Textmetadata
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.