Evidence map›Paper›PMID 30227835›Full record

ArticleBMC cancer2018

Diagnostic role of circulating extracellular matrix-related proteins in non-small cell lung cancer.

Francesca Andriani, Elena Landoni, Mavis Mensah, Federica Facchinetti, Rosalba Miceli, Elda Tagliabue, Marta Giussani, Maurizio Callari, Loris De Cecco, Mario Paolo Colombo and 3 more

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 9% 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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 52 citations in OpenAlex.

  1. Pooled it
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  12. LC-MS/MS method for proline-glycine-proline and acetylated proline-glycine-proline in human plasma.Journal of chromatography. B, Analytical technologies in the biomedical and life sciences · 2023
    Article
  13. Plasma SPARC Elevation in Delayed Cerebral Ischemia After Aneurysmal Subarachnoid Hemorrhage.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2023
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 2 institutions in 2 countries.

Francesca AndrianiDepartment of Research, Tumor Genomics Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Via Venezian 1, 20133, Milan, Italy.
Elena LandoniDepartment of Applied Research and Technical Development, Medical Statistics and Biometry Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Mavis MensahDepartment of Research, Tumor Genomics Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Via Venezian 1, 20133, Milan, Italy.
Federica FacchinettiDepartment of Research, Tumor Genomics Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Via Venezian 1, 20133, Milan, Italy.
Rosalba MiceliDepartment of Applied Research and Technical Development, Medical Statistics and Biometry Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Elda TagliabueDepartment of Research, Molecular Targeting Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Marta GiussaniDepartment of Research, Molecular Targeting Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Maurizio CallariDepartment of Applied Research and Technical Development, Biomarkers, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Loris De CeccoDepartment of Applied Research and technical Development, Genomics, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Mario Paolo ColomboDepartment of Research, Molecular Immunology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, 20133, Milan, Italy.
Luca RozDepartment of Research, Tumor Genomics Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Via Venezian 1, 20133, Milan, Italy.
Ugo PastorinoDepartment of Surgery, Thoracic Surgery Unit Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Gabriella SozziDepartment of Research, Tumor Genomics Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Via Venezian 1, 20133, Milan, Italy. gabriella.sozzi@istitutotumori.mi.it.ORCID http://orcid.org/0000-0001-9360-6914
Fondazione IRCCS Istituto Nazionale dei Tumori · ITUniversity of Cambridge · GB

Funding

Associazione Italiana per la Ricerca sul Cancro 12162Associazione Italiana per la Ricerca sul Cancro 14318Associazione Italiana per la Ricerca sul Cancro 16847Associazione Italiana per la Ricerca sul Cancro 18812
6 · The paper itself

Abstract

backgroundInteractions between cancer cells and the surrounding microenvironment are crucial determinants of cancer progression. During this process, bi-directional communication among tumor cells and cancer associated fibroblasts (CAF) regulate extracellular matrix (ECM) deposition and remodeling. As a result of this dynamic process, soluble ECM proteins can be released into the bloodstream and may represent novel circulating biomarkers useful for cancer diagnosis. The aim of the present study was to measure the levels of three circulating ECM related proteins (COL11A1, COL10A1 and SPARC) in plasma samples of lung cancer patients and in healthy heavy-smokers controls and test whether such measurements have diagnostic or prognostic value.

methodsGene expression profiling of lung fibroblasts isolated from paired normal and cancer tissue of NSCLC patients was performed by gene expression microarrays. The prioritization of the candidates for the study of circulating proteins in plasma was based on the most differentially expressed genes in cancer associated fibroblasts. Soluble ECM proteins were assessed by western blot in the conditioned medium of lung fibroblasts and by ELISA assays in plasma samples.

resultsPlasma samples from lung cancer patients and healthy heavy-smokers controls were tested for levels of COL11A1 and COL10A1 (n = 57 each) and SPARC (n = 90 each). Higher plasma levels of COL10A1 were detected in patients (p ≤ 0.001), a difference that was driven specifically by females (p < 0.001). No difference in COL11A1 levels between patients and controls was found. SPARC levels were also higher in plasma patients than controls (p < 0.001) with good performance in discriminating the two groups (AUC = 0.744). No significant association was observed between plasma proteins levels and clinicopathological features or survival.

conclusionSoluble factors related to proficient tumor-stroma cross-talk are detectable in plasma of primary lung cancer patients and may represent a valuable complementary diagnostic tool to discriminate lung cancer patients from healthy heavy-smokers individuals as shown for the SPARC protein.

Indexed as

AgedCarcinoma, Non-Small-Cell LungCirculating Tumor DNACollagen Type XCollagen Type XIDisease-Free SurvivalExtracellular MatrixExtracellular Matrix ProteinsFemaleGene Expression Regulation, NeoplasticHumansMaleMiddle AgedOsteonectinPrognosisSex CharacteristicsCirculating Tumor DNACOL11A1 protein, humanCollagen Type XCollagen Type XIExtracellular Matrix ProteinsOsteonectinSPARC protein, humanCAFCancer associated fibroblastsCirculating biomarkersExtracellular matrix (ECM)Lung cancerSecreted protein acidic and rich in cysteineSPARC

Identifiers

PMID30227835
PMCPMC6145327
OpenAlexW2891227499

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.