Evidence map›Paper›PMID 37697316›Full record

ArticleWorld journal of surgical oncology2023

The importance of CXCR4 expression in tumor stroma as a potential biomarker in pancreatic cancer.

Raquel Bodoque-Villar, David Padilla-Valverde, Lucía María González-López, José Ramón Muñoz-Rodríguez, Javier Arias-Pardilla, Clara Villar-Rodríguez, Francisco Javier Gómez-Romero, Gema Verdugo-Moreno, Francisco Javier Redondo-Calvo, Leticia Serrano-Oviedo

Open access · goldAbstract read
In one paragraph

Article in World journal of surgical oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.2field-weighted citation impact, top 18% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Exploring G Protein-Coupled Receptors in Hematological Cancers.ACS pharmacology & translational science · 2024
    Article
  3. Article
  4. Review
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

10 authors at 3 institutions in 1 country.

Raquel Bodoque-VillarTraslational Investigation Unit, University General Hospital of Ciudad Real, SESCAM, Ciudad Real, Spain.
David Padilla-ValverdeTraslational Investigation Unit, University General Hospital of Ciudad Real, SESCAM, Ciudad Real, Spain.
Lucía María González-LópezTraslational Investigation Unit, University General Hospital of Ciudad Real, SESCAM, Ciudad Real, Spain.
José Ramón Muñoz-RodríguezTraslational Investigation Unit, University General Hospital of Ciudad Real, SESCAM, Ciudad Real, Spain.
Javier Arias-PardillaTraslational Investigation Unit, University General Hospital of Ciudad Real, SESCAM, Ciudad Real, Spain.
Clara Villar-RodríguezTraslational Investigation Unit, University General Hospital of Ciudad Real, SESCAM, Ciudad Real, Spain.
Francisco Javier Gómez-RomeroTraslational Investigation Unit, University General Hospital of Ciudad Real, SESCAM, Ciudad Real, Spain.
Gema Verdugo-MorenoTraslational Investigation Unit, University General Hospital of Ciudad Real, SESCAM, Ciudad Real, Spain.
Francisco Javier Redondo-CalvoTraslational Investigation Unit, University General Hospital of Ciudad Real, SESCAM, Ciudad Real, Spain.
Leticia Serrano-OviedoTraslational Investigation Unit, University General Hospital of Ciudad Real, SESCAM, Ciudad Real, Spain. lserranoo@sescam.jccm.es.
Hospital General Universitario de Ciudad Real · ESServicio de Salud de Castilla La Mancha · ESUniversity of Castilla-La Mancha · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPancreatic ductal adenocarcinoma (PDAC) is one of the main causes of cancer mortality in the world. A characteristic feature of this cancer is that a large part of the tumor volume is composed of a stroma with different cells and factors. Among these, we can highlight the cytokines, which perform their function through binding to their receptors. Given the impact of the CXCR4 receptor in the interactions between tumor cells and their microenvironment and its involvement in important signaling pathways in cancer, it is proposed as a very promising prognostic biomarker and as a goal for new targeted therapies. Numerous studies analyze the expression of CXCR4 but we suggest focusing on the expression of CXCR4 in the stroma.

methodsExpression of CXCR4 in specimens from 33 patients with PDAC was evaluated by immunohistochemistry techniques and matched with clinicopathological parameters, overall and disease-free survival rates.

resultsThe percentage of stroma was lower in non-tumor tissue (32.4 ± 5.2) than in tumor pancreatic tissue (67.4 ± 4.8), P-value = 0.001. The level of CXCR4 expression in stromal cells was diminished in non-tumor tissue (8.7 ± 4.6) and higher in tumor pancreatic tissue (23.5 ± 6.1), P-value = 0.022. No significant differences were identified in total cell count and inflammatory cells between non-tumor tissue and pancreatic tumor tissue. No association was observed between CXCR4 expression and any of the clinical or pathological data, overall and disease-free survival rates. Analyzing exclusively the stroma of tumor samples, the CXCR4 expression was associated with tumor differentiation, P-value = 0.05.

conclusionsIn this study, we reflect the importance of CXCR4 expression in the stroma of patients diagnosed with PDAC. Our results revealed a high CXCR4 expression in the tumor stroma, which is related to a poor tumor differentiation. On the contrary, we could not find an association between CXCR4 expression and survival and the rest of the clinicopathological variables. Focusing the study on the CXCR4 expression in the tumor stroma could generate more robust results. Therefore, we consider it key to develop more studies to enlighten the role of this receptor in PDAC and its implication as a possible biomarker.

Indexed as

Carcinoma, Pancreatic DuctalPancreatic NeoplasmsBiomarkers, TumorHumansReceptors, CXCR4Tumor MicroenvironmentBiomarkers, TumorCXCR4 protein, humanReceptors, CXCR4ChemokinesCXCR4/CXCL12ImmunohistochemistryPancreatic ductal adenocarcinoma

Identifiers

PMID37697316
PMCPMC10496205
OpenAlexW4386594470

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.