Evidence map›Paper›PMID 40261622›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2025

Using Zymography to Assess Circulating Matrix Metalloproteinase (MMP)-2 and MMP-9 in Clinical Samples.

Sandra O Conde-Tella, Raquel F Gerlach, Jose E Tanus-Santos

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Article in Methods in molecular biology (Clifton, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Sandra O Conde-TellaDepartment of Pharmacology, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, SP, Brazil.
Raquel F GerlachDepartment of Basic and Oral Biology, FORP, University of Sao Paulo, Ribeirao Preto, SP, Brazil.
Jose E Tanus-SantosDepartment of Pharmacology, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, SP, Brazil. tanus@fmrp.usp.br.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Matrix metalloproteinases (MMPs) are a family of zinc-dependent proteinases that cleave a variety of different substrates and play key roles in both physiological and pathological processes. They are involved in the pathophysiology of many disease conditions, and for this reason, many clinical studies have been carried out to examine whether circulating MMP concentrations reflect the severity of disease conditions. This article presents detailed information that is critical to assess circulating MMP-2 and MMP-9 activity in clinical samples by using zymography, which is a powerful technique that has been used for more than three decades to detect picogram quantities of MMPs. Important methodological issues have been addressed in the past regarding this technique, and some analytical and preanalytical details may severely affect the results and thus hamper the diagnostic and prognostic value of such measurements. While fasting or storing plasma samples for 1 month at -20 °C or at -70 °C does not significantly affect plasma MMP-2 or MMP-9 activity, repeating freeze-thaw cycles of plasma samples decrease MMP-9 activity after seven cycles. Importantly, the appropriate volume to assess MMP-2 is significantly lower than the appropriate volume to assess MMP-9 activity. Finally, special concerns exist with respect to circulating MMP-9 (but not MMP-2) measurements, which are found at artificially higher concentrations in serum than in plasma (EDTA, citrate or heparin) samples, even though significant correlations exist between MMP-9 levels assessed in plasma and in serum samples.

Indexed as

Enzyme AssaysMatrix Metalloproteinase 2Matrix Metalloproteinase 9HumansMatrix Metalloproteinase 2Matrix Metalloproteinase 9MMP2 protein, humanMMP9 protein, humanClinical studiesMatrix metalloproteinase-2Matrix metalloproteinase-9PlasmaSerumZymography

Identifiers

PMID40261622

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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.