Evidence map›Paper›PMID 24194920›Full record

ArticlePloS one2013

Overexpression of COL11A1 by cancer-associated fibroblasts: clinical relevance of a stromal marker in pancreatic cancer.

Carmen García-Pravia, José A Galván, Natalia Gutiérrez-Corral, Lorena Solar-García, Eva García-Pérez, Marcos García-Ocaña, Jokin Del Amo-Iribarren, Primitiva Menéndez-Rodríguez, Juan García-García, Juan R de Los Toyos and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
1.7field-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

54 citing papers in PubMed, 93 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

12 authors at 4 institutions in 1 country.

Carmen García-PraviaPathological Anatomy Service, Hospital Universitario Central de Asturias (HUCA), Oviedo, Spain ; Instituto Universitario de Oncología del Principado de Asturias (IUOPA), Oviedo, Spain.
José A Galván
Natalia Gutiérrez-Corral
Lorena Solar-García
Eva García-Pérez
Marcos García-Ocaña
Jokin Del Amo-Iribarren
Primitiva Menéndez-Rodríguez
Juan García-García
Juan R de Los Toyos
Laureano Simón-Buela
Luis Barneo
Hospital Universitario Central de Asturias · ESUniversidad de Oviedo · ESInstituto de Investigación Sanitaria del Principado de Asturias · ESOncomatryx (Spain) · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe collagen11A1 (COL11A1) gene is overexpressed in pancreatic cancer. The expression of COL11A1 protein could be involved in desmoplastic events in pancreatic cancer, but an antibody that specifically stains the COL11A1 protein is not currently available. METHODS AND

findingsA total of 54 pancreatic ductal adenocarcinomas (PDAC), 23 chronic pancreatitis (CP) samples, and cultured peritumoral stromal cells of PDAC (passages 3-6) were studied. Normal human pancreas tissue samples were obtained through a cadaveric organ donation program. 1) Validation of COL11A1 gene overexpression by q-RT-PCR.

findingsthe expression of COL11A1 gene is significantly increased in PDAC samples vs. normal and CP samples. 2) Analysis of COL11A1 by immunohistochemistry using highly specific anti-proCOL11A1 antibodies.

findingsanti-proCOL11A1 stains stromal cells/cancer-associated fibroblasts (CAFs) of PDAC but it does not stain chronic benign condition (chronic pancreatitis) stromal cells, epithelial cells, or normal fibroblasts. 3) Evaluation of the discrimination ability of the antibody.

findingsanti-proCOL11A1 immunostaining accurately discriminates between PDAC and CP (AUC 0.936, 95% CI 0.851, 0.981). 4) Phenotypic characterization of proCOL11A1+ stromal cells co-staining with mesenchymal, epithelial and stellate cell markers on pancreatic tissue samples and cultured peritumoral pancreatic cancer stromal cells.

findingsProCOL11A1+ cells present co-staining with mesenchymal, stellate and epithelial markers (EMT phenotype) in different proportions. CONCLUSIONS/SIGNIFICANCE: Detection of proCOL11A1 through immunostaining with this newly-developed antibody allows for a highly accurate distinction between PDAC and CP. Unlike other available antibodies commonly used to detect CAFs, anti-proCOL11A1 is negative in stromal cells of the normal pancreas and almost absent in benign inflammation. These results strongly suggest that proCOL11A1 is a specific marker for CAFs, and thus, anti-proCOL11A1 is a powerful new tool for cancer research and clinical diagnostics.

Indexed as

AnimalsAntibodies, MonoclonalArea Under CurveBiomarkers, TumorCarcinoma, Pancreatic DuctalCollagen Type XIDNA PrimersGene Expression Regulation, NeoplasticHumansImmunohistochemistryMiceMicroscopy, FluorescencePancreatic NeoplasmsReal-Time Polymerase Chain ReactionROC CurveStromal CellsAntibodies, MonoclonalBiomarkers, TumorCOL11A1 protein, humanCollagen Type XIDNA Primers

Identifiers

PMID24194920
PMCPMC3808536
OpenAlexW1496645584

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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.