Evidence map›Paper›PMID 33363615›Full record

ArticleOncology letters2021

Prognostic role of matrix metalloproteinase 9 in early breast cancer.

Katarina Kalavska, Zuzana Cierna, Marian Karaba, Gabriel Minarik, Juraj Benca, Tatiana Sedlackova, Denisa Kolekova, Ivana Mrvova, Daniel Pindak, Jozef Mardiak and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.7field-weighted citation impact, top 35% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
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  5. Substrate O-glycosylation actively regulates extracellular proteolysis.Protein science : a publication of the Protein Society · 2024
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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 2 institutions in 1 country.

Katarina KalavskaTranslational Research Unit, Faculty of Medicine, Comenius University, 833 10 Bratislava, Slovakia.
Zuzana CiernaDepartment of Pathology, Faculty of Medicine, Comenius University, 811 08 Bratislava, Slovakia.
Marian KarabaDepartment of Oncosurgery, National Cancer Institute, 833 10 Bratislava, Slovakia.
Gabriel MinarikInstitute of Molecular Biomedicine, Faculty of Medicine, Comenius University, 811 08 Bratislava, Slovakia.
Juraj BencaDepartment of Oncosurgery, National Cancer Institute, 833 10 Bratislava, Slovakia.
Tatiana SedlackovaGeneton Ltd., 841 04 Bratislava, Slovakia.
Denisa KolekovaTranslational Research Unit, Faculty of Medicine, Comenius University, 833 10 Bratislava, Slovakia.
Ivana MrvovaDepartment of Pathology, Faculty of Medicine, Comenius University, 811 08 Bratislava, Slovakia.
Daniel PindakDepartment of Oncosurgery, National Cancer Institute, 833 10 Bratislava, Slovakia.
Jozef MardiakSecond Department of Oncology, Faculty of Medicine, Comenius University, National Cancer Institute, 833 10 Bratislava, Slovakia.
Michal MegoTranslational Research Unit, Faculty of Medicine, Comenius University, 833 10 Bratislava, Slovakia.
Comenius University Bratislava · SKGeneton (Slovakia) · SK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MMP9 is involved in extracellular matrix degradation during various physiological and pathological conditions, including tumorigenesis. The present study aimed to assess the prognostic role of intratumoral MMP9 and to determine its association with circulating tumor cells (CTCs) in patients with early breast cancer. A total of 318 patients with primary breast cancer (PBC) were enrolled into the present study. Specimens were subjected to immunohistochemistry analysis, using the MMP9 monoclonal antibody. MMP9 expression was scored using a weighted histoscore (WH). The results demonstrated that the mean WH ± SEM for MMP9 expression was significantly higher in breast tumor cells compared with tumor associated stromas (132.0±5.2 vs. 50.8±3.7; P<0.00001). Furthermore, a positive association was observed between MMP9 expression, the hormone positive status and proliferation index of analysed breast cancer tumour cells. Notably, the prognostic role of MMP9 was not observed in tumor cells [hazard ratio (HR) =0.96; 95% confidence interval (CI), 0.58-1.59; P=0.864] or tumor associated stroma (HR=1.29; 95% CI, 0.60-2.78; P=0.547). Subgroup analysis demonstrated that patients that were HR negative or triple negative, with low MMP9 expression in tumor cells and stroma had a significantly improved disease-free survival than patients with high MMP9 expression. Taken together, the results of the present study demonstrated that high MMP9 expression in PBC was associated with favorable tumor characteristics. However, the prognostic value of MMP9 was limited to only the HR negative and CTC epithelial-to-mesenchymal transition positive subgroups. Thus, analyzing MMP9 tumor expression may help identify patients with increased risk of disease recurrence in these subgroups.

Indexed as

circulating tumor cellsearly breast cancermatrix-metalloproteinase 9prognostic value

Identifiers

PMID33363615
PMCPMC7723168
OpenAlexW3109379722

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.