Evidence map›Paper›PMID 25580640›Full record

ArticleCancer science2015

Overexpression of chemokine receptor CXCR2 and ligand CXCL7 in liver metastases from colon cancer is correlated to shorter disease-free and overall survival.

Thibault Desurmont, Nicolas Skrypek, Alain Duhamel, Nicolas Jonckheere, Guillaume Millet, Emmanuelle Leteurtre, Pierre Gosset, Belinda Duchene, Nassima Ramdane, Mohamed Hebbar and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 5% 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

47 citing papers in PubMed, 1 synthesis or guideline pooled it, 71 citations in OpenAlex.

  1. Pooled it
  2. Chemokine receptor CXCR2 and plasminogen activator inhibitor-1 expression in colorectal adenocarcinoma are associated with prognostic features.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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  10. Expression ofTranslational cancer research · 2022
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  18. Regulation and functional roles of chemokines in liver diseases.Nature reviews. Gastroenterology & hepatology · 2021
    Review
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  20. 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

14 authors at 5 institutions in 1 country.

Thibault DesurmontInserm, U837, Team-5 (Mucins, Epithelial Differentiation, and Carcinogenesis), Jean-Pierre Aubert Research Centre, Université Lille, France; Department of Digestive and Visceral Surgery, GHICL, Saint-Vincent de Paul Hospital, Lille, France.
Nicolas Skrypek
Alain Duhamel
Nicolas Jonckheere
Guillaume Millet
Emmanuelle Leteurtre
Pierre Gosset
Belinda Duchene
Nassima Ramdane
Mohamed Hebbar
Isabelle Van Seuningen
François-René Pruvot
Guillemette Huet
Stéphanie Truant
Centre de Recherche Jean Pierre Aubert · FRCentre Hospitalier Universitaire de Lille · FRInserm · FRGroupe Hospitalier de l'Institut Catholique de Lille · FRUniversité Lille Nord de France · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Our aim was to analyze the potential role of chemokine receptors CXCR2 and CXCR4 signalling pathways in liver metastatic colorectal cancer (CRC) relapse. CXCR2, CXCR4, and their chemokine ligands were evaluated in liver metastases of colorectal cancer in order to study their correlation with overall and disease-free survival of patients having received, or not received, a neoadjuvant chemotherapy regimen. Quantitative RT-PCR and CXCR2 immunohistochemical staining were carried out using CRC liver metastasis samples. Expression levels of CXCR2, CXCR4, and their ligands were statistically analyzed according to treatment with neoadjuvant chemotherapy and patients' outcome. CXCR2 and CXCL7 overexpression are correlated to shorter overall and disease-free survival. By multivariate analysis, CXCR2 and CXCL7 expressions are independent factors of overall and disease-free survival. Neoadjuvant chemotherapy increases significantly the expression of CXCR2: treated group 1.89 (0.02-50.92) vs 0.55 (0.07-3.22), P = 0.016. CXCL7 was overexpressed close to significance, 0.40 (0.00-7.85) vs 0.15 (0.01-7.88), P = 0.12. We show the involvement of CXCL7/CXCR2 signalling pathways as a predictive factor of poor outcome in metastatic CRC. 5-Fluorouracil-based chemotherapy regimens increase the expression of these genes in liver metastasis, providing one explanation for aggressiveness of relapsed drug-resistant tumors. Selective blockage of CXCR2/CXCL7 signalling pathways could provide new potential therapeutic opportunities.

Indexed as

Antineoplastic Combined Chemotherapy Protocolsbeta-ThromboglobulinCamptothecinCapecitabineColonic NeoplasmsDeoxycytidineDisease-Free SurvivalFemaleFluorouracilHumansLeucovorinLiver NeoplasmsMaleMiddle AgedNeoadjuvant TherapyNeoplasm Recurrence, Localbeta-ThromboglobulinCamptothecinCapecitabineCXCR4 protein, humanDeoxycytidineFluorouracilLeucovorinOrganoplatinum CompoundsPPBP protein, humanReceptors, CXCR4Receptors, Interleukin-8B5FU-based chemotherapycolorectal cancerCXCL7CXCR2liver metastasis

Identifiers

PMID25580640
PMCPMC4376434
OpenAlexW2010740201

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.