Evidence map›Paper›PMID 29207990›Full record

ArticleBMC cancer2017

Relevance of matrix metalloproteases in non-small cell lung cancer diagnosis.

Sonia Blanco-Prieto, Leticia Barcia-Castro, María Páez de la Cadena, Francisco Javier Rodríguez-Berrocal, Lorena Vázquez-Iglesias, María Isabel Botana-Rial, Alberto Fernández-Villar, Loretta De Chiara

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 21% 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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 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

8 authors at 2 institutions in 1 country.

Sonia Blanco-PrietoDepartment of Biochemistry, Genetics and Immunology, Universidade de Vigo.Vigo, As Lagoas-Marcosende s/n, 36310, Vigo, Spain.
Leticia Barcia-CastroDepartment of Biochemistry, Genetics and Immunology, Universidade de Vigo.Vigo, As Lagoas-Marcosende s/n, 36310, Vigo, Spain.
María Páez de la CadenaDepartment of Biochemistry, Genetics and Immunology, Universidade de Vigo.Vigo, As Lagoas-Marcosende s/n, 36310, Vigo, Spain.
Francisco Javier Rodríguez-BerrocalDepartment of Biochemistry, Genetics and Immunology, Universidade de Vigo.Vigo, As Lagoas-Marcosende s/n, 36310, Vigo, Spain.
Lorena Vázquez-IglesiasDepartment of Biochemistry, Genetics and Immunology, Universidade de Vigo.Vigo, As Lagoas-Marcosende s/n, 36310, Vigo, Spain.
María Isabel Botana-RialDepartment of Pneumology of Hospital Álvaro Cunqueiro EOXI Vigo, Carretera Clara Campoamor, 341, 36212, Vigo, Spain.
Alberto Fernández-VillarDepartment of Pneumology of Hospital Álvaro Cunqueiro EOXI Vigo, Carretera Clara Campoamor, 341, 36212, Vigo, Spain.
Loretta De ChiaraDepartment of Biochemistry, Genetics and Immunology, Universidade de Vigo.Vigo, As Lagoas-Marcosende s/n, 36310, Vigo, Spain. ldechiara@uvigo.es.
Universidade de Vigo · ESUniversity Hospital Complex Of Vigo · ES

Funding

Consellería de Cultura, Educación e Ordenación Universitaria, Xunta de Galicia GRC2014/019Consellería de Cultura, Educación e Ordenación Universitaria, Xunta de Galicia INBIOMED 2012-273Instituto de Salud Carlos III PS09-00405Spanish Ministry of Science and Innovation FPU
6 · The paper itself

Abstract

backgroundThe need for novel biomarkers that could aid in non-small cell lung cancer (NSCLC) detection, together with the relevance of Matrix Metalloproteases (MMPs) -1, -2, -7, -9 and -10 in lung tumorigenesis, prompted us to assess the diagnostic usefulness of these MMPs and the Tissue Inhibitor of Metalloproteinase (TIMP) -1 in NSCLC patients.

methodsMarkers were evaluated in an initial study cohort (19 NSCLC cases and 19 healthy controls). Those that better performed were analyzed in a larger sample including patients with benign lung diseases. Serum MMPs and TIMP-1 were determined by multiplexed immunoassays. Logistic regression was employed for multivariate analysis of biomarker combinations.

resultsMMPs and TIMP-1 were elevated in the serum of NSCLC patients compared to healthy controls. MMP-1, -7 and -9 performed at best and were further evaluated in the sample including benign pathologies, corroborating the superiority of MMP-9 in NSCLC discrimination, also at early-stage NSCLC. The optimal diagnostic value was obtained with the model including MMP-9, gender, age and smoking history, that demonstrated an AUC of 0.787, 85.54% sensitivity and 64.89% specificity.

conclusionOur results suggest that MMP-9 is a potential biomarker for NSCLC diagnosis and its combined measurement with other biomarkers could improve NSCLC detection.

Indexed as

AdultAgedAged, 80 and overBiomarkers, TumorCarcinoma, Non-Small-Cell LungCase-Control StudiesFemaleHumansLung NeoplasmsMaleMatrix Metalloproteinases, SecretedMiddle AgedTissue Inhibitor of Metalloproteinase-1Young AdultBiomarkers, TumorMatrix Metalloproteinases, SecretedTIMP1 protein, humanTissue Inhibitor of Metalloproteinase-1DiagnosisMatrix metalloproteasesNon-small cell lung cancerSerum biomarkers

Identifiers

PMID29207990
PMCPMC5718060
OpenAlexW2772023181

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.