Evidence map›Paper›PMID 25250855›Full record

ArticleAmerican journal of respiratory and critical care medicine2014

Matrix metalloproteinase-19 promotes metastatic behavior in vitro and is associated with increased mortality in non-small cell lung cancer.

Guoying Yu, Jose D Herazo-Maya, Tomoko Nukui, Marjorie Romkes, Anil Parwani, Brenda M Juan-Guardela, Jennifer Robertson, Jack Gauldie, Jill M Siegfried, Naftali Kaminski and 1 more

Open access · greenAbstract read
In one paragraph

Article in American journal of respiratory and critical care medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
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

42 citing papers in PubMed, 94 citations in OpenAlex.

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  18. MicroRNAs: The Link between the Metabolic Syndrome and Oncogenesis.International journal of molecular sciences · 2021
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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

11 authors at 5 institutions in 2 countries.

Guoying Yu1 Section of Pulmonary, Critical Care and Sleep Medicine, Yale School of Medicine, New Haven, Connecticut.
Jose D Herazo-Maya
Tomoko Nukui
Marjorie Romkes
Anil Parwani
Brenda M Juan-Guardela
Jennifer Robertson
Jack Gauldie
Jill M Siegfried
Naftali Kaminski
Daniel J Kass
Yale University · USUniversity of Pittsburgh · USMcMaster University · CAPulmonary and Allergy Associates · USUniversity of Minnesota · US

Funding

VECTOR CORE FACILITYP30CA047904 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Jessie Nedrow · 1988 to 2026
$158.0M
The Emphysematous Microenvironment Promotes Lung Tumorigenesis and ProgressionR01HL107883 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SHAPIRO, STEVEN D · 2011 to 2014
$2.7M
NCI NIH HHS P30 CA047904NCI NIH HHS P30CA047904NHLBI NIH HHS R01 HL107883NHLBI NIH HHS R01HL107883
6 · The paper itself

Abstract

rationaleLung cancer is the leading cause of cancer death in both men and women in the United States and worldwide. Matrix metalloproteinases (MMPs) have been implicated in the development and progression of lung cancer, but their role in the molecular pathogenesis of lung cancer remains unclear. We have found that MMP19, a relatively novel member of the MMP family, is overexpressed in lung tumors when compared with control subjects.

objectivesTo test the hypothesis that MMP19 plays a significant role in the development and progression of non-small cell lung cancer (NSCLC).

methodsWe have analyzed lung cancer gene expression data, immunostained lung tumors for MMP19, and performed in vitro assays to test the effects of MMP19 in NSCLC cells. MEASUREMENTS AND MAIN

resultsWe found that MMP19 gene and protein expression is increased in lung cancer tumors compared with adjacent and histologically normal lung tissues. In three independent datasets, increased MMP19 gene expression conferred a poorer prognosis in NSCLC. In vitro, we found that overexpression of MMP19 promotes epithelial-mesenchymal transition, migration, and invasiveness in multiple NSCLC cell lines. Overexpression of MMP19 with a mutation at the catalytic site did not impair epithelial-mesenchymal transition or expression of prometastasis genes. We also found that miR-30 isoforms, a microRNA family predicted to target MMP19, is markedly down-regulated in human lung cancer and regulates MMP19 expression.

conclusionsTaken together, these findings suggest that MMP19 is associated with the development and progression of NSCLC and may be a potential biomarker of disease severity and outcome.

Indexed as

ApoptosisCarcinoma, Non-Small-Cell LungCell DeathCell Line, TumorDown-RegulationEpithelial-Mesenchymal TransitionFemaleGene Expression Regulation, NeoplasticHumansLung NeoplasmsMaleMatrix Metalloproteinases, SecretedMicroRNAsNeoplasm InvasivenessSurvival Ratematrix metalloproteinase 19Matrix Metalloproteinases, SecretedMicroRNAsepithelial–mesenchymal transitionmetastasismiR-30MMP19non–small cell lung cancer

Identifiers

PMID25250855
PMCPMC4299607
OpenAlexW2144832461

What OpenQuestion holds

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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.