Evidence map›Paper›PMID 31282404›Full record

ArticleCancer biomarkers : section A of Disease markers2019

Polymorphisms in MMP-14 and MMP-2 genes and ovarian cancer survival.

M Caroline Vos, Angela van Tilborg, William J Brands, Dorry Boll, Dennis van Hamont, Hans van der Putten, Brenda Pijlman, Anneke A M van der Wurff, Toin H van Kuppevelt, Leon F A G Massuger

Abstract read
In one paragraph

Article in Cancer biomarkers : section A of Disease markers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 48% 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

1 citing paper in PubMed, 1 synthesis or guideline pooled it, 6 citations in OpenAlex.

  1. Pooled it
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 5 institutions in 1 country.

M Caroline VosDepartment of Obstetrics and Gynaecology, Elisabeth-Tweesteden Hospital, 5000 LC Tilburg, the Netherlands.
Angela van TilborgDepartment of Obstetrics and Gynaecology and Department of Pathology, Radboud University Nijmegen Medical Centre, 6500 HB Nijmegen, the Netherlands.
William J BrandsDepartment of Pathology, Elisabeth-Tweesteden Hospital, 5000 LC Tilburg, the Netherlands.
Dorry BollDepartment of Obstetrics and Gynaecology, Elisabeth-Tweesteden Hospital, 5000 LC Tilburg, the Netherlands.
Dennis van HamontDepartment of Obstetrics and Gynaecology, Amphia Ziekenhuis, Breda, the Netherlands.
Hans van der PuttenDepartment of Obstetrics and Gynaecology, Catharina Hospital, Eindhoven, the Netherlands.
Brenda PijlmanDepartment of Obstetrics and Gynaecology, Jeroen Bosch Ziekenhuis, s-Hertogenbosch, the Netherlands.
Anneke A M van der WurffDepartment of Pathology, Elisabeth-Tweesteden Hospital, 5000 LC Tilburg, the Netherlands.
Toin H van KuppeveltDepartment of Biochemistry, Radboud Institute for Molecular Life Sciences, Radboud University Medical Centre, 6500 HB Nijmegen, the Netherlands.
Leon F A G MassugerDepartment of Obstetrics and Gynaecology, Radboud University Nijmegen Medical Centre, 6500 HB Nijmegen, the Netherlands.
Elisabeth-TweeSteden Ziekenhuis · NLRadboud University Medical Center · NLRadboud University Nijmegen · NLAmphia Ziekenhuis · NLJeroen Bosch Ziekenhuis · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFunctional polymorphisms in matrix metalloproteinases can increase or decrease the risk of cancer. This study focused on ovarian cancer and investigated how polymorphisms in the coding region of MMP-14 and the promoter region of MMP-2 are related to clinical characteristics including survival.

methodsIn 144 patients with ovarian tumours from a Caucasian population, polymorphisms of MMP-14 (+7096 and +6767) and MMP-2 (-735 and -1306) were analysed. These results were then correlated to the immunohistochemical expression of MMP-14 and MMP-2 and clinical characteristics.

resultsIn these patients, the MMP-14 +7096 polymorphism showed only TT genotype, in sharp contrast to the described MAF (minimal allele frequency) C of 27%. The MMP-14 +6767 G>A polymorphism was found to have a hazard ratio of 2.09 (CI 1.00-4.35, p 0.046) for recurrence-free survival in advanced-stage patients. However, this significance disappeared after Bonferroni correction for multiple testing. No other correlations between MMP-14 and MMP-2 polymorphisms, immunohistochemistry and clinical characteristics were found, except between the MMP-2 -1306 polymorphism and differentiation grade, with a Spearman correlation coefficient of -0.19, p 0.064.

conclusionsIn ovarian cancer, the MMP-14 +6767 G>A polymorphism in the coding region seems to improve recurrence-free survival with a hazard ratio of 2.09 (CI 1.00-4.35, p 0.046). However, as this significance disappeared after correction for multiple testing, there is a need for further research on the functional effect of this change in the MMP-14 gene with larger patient sample sizes.

Indexed as

Genetic Predisposition to DiseaseAdultDisease-Free SurvivalFemaleGene FrequencyGenotypeHumansMatrix Metalloproteinase 14Matrix Metalloproteinase 2Middle AgedOvarian NeoplasmsPolymorphism, Single NucleotideMatrix Metalloproteinase 14Matrix Metalloproteinase 2MMP-14MMP-2ovarian cancerpolymorphisms

Identifiers

PMID31282404
PMCPMC13082425
OpenAlexW2953746648

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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.