Evidence map›Paper›PMID 41931149›Full record

ArticleClinical and experimental medicine2026

Opposing prognostic roles of tumor-associated and circulating MMP8 in colorectal cancer.

Iivari Loukasmäki, Anne Tuomisto, Päivi Sirniö, Meeri Kastinen, Henna Karjalainen, Ville K Äijälä, Vilja V Tapiainen, Taina Tervahartiala, Timo Sorsa, Vesa-Matti Pohjanen and 8 more

Abstract read
In one paragraph

Article in Clinical and experimental medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
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

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

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

18 authors.

Iivari LoukasmäkiTranslational Medicine Research Unit, Medical Research Center Oulu, Oulu University Hospital, University of Oulu, Aapistie 5A, 90220, Oulu, Finland.
Anne TuomistoTranslational Medicine Research Unit, Medical Research Center Oulu, Oulu University Hospital, University of Oulu, Aapistie 5A, 90220, Oulu, Finland.
Päivi SirniöTranslational Medicine Research Unit, Medical Research Center Oulu, Oulu University Hospital, University of Oulu, Aapistie 5A, 90220, Oulu, Finland.
Meeri KastinenTranslational Medicine Research Unit, Medical Research Center Oulu, Oulu University Hospital, University of Oulu, Aapistie 5A, 90220, Oulu, Finland.
Henna KarjalainenTranslational Medicine Research Unit, Medical Research Center Oulu, Oulu University Hospital, University of Oulu, Aapistie 5A, 90220, Oulu, Finland.
Ville K ÄijäläTranslational Medicine Research Unit, Medical Research Center Oulu, Oulu University Hospital, University of Oulu, Aapistie 5A, 90220, Oulu, Finland.
Vilja V TapiainenTranslational Medicine Research Unit, Medical Research Center Oulu, Oulu University Hospital, University of Oulu, Aapistie 5A, 90220, Oulu, Finland.
Taina TervahartialaDepartment of Oral and Maxillofacial Diseases, Institute of Dentistry, Helsinki University Central Hospital, Helsinki, Finland.
Timo SorsaDepartment of Oral and Maxillofacial Diseases, Institute of Dentistry, Helsinki University Central Hospital, Helsinki, Finland.
Vesa-Matti PohjanenTranslational Medicine Research Unit, Medical Research Center Oulu, Oulu University Hospital, University of Oulu, Aapistie 5A, 90220, Oulu, Finland.
Taneli T MattilaTranslational Medicine Research Unit, Medical Research Center Oulu, Oulu University Hospital, University of Oulu, Aapistie 5A, 90220, Oulu, Finland.
Outi LindgrenTranslational Medicine Research Unit, Medical Research Center Oulu, Oulu University Hospital, University of Oulu, Aapistie 5A, 90220, Oulu, Finland.
Jukka RintalaTranslational Medicine Research Unit, Medical Research Center Oulu, Oulu University Hospital, University of Oulu, Aapistie 5A, 90220, Oulu, Finland.
Sanna MeriläinenTranslational Medicine Research Unit, Medical Research Center Oulu, Oulu University Hospital, University of Oulu, Aapistie 5A, 90220, Oulu, Finland.
Juha SaarnioTranslational Medicine Research Unit, Medical Research Center Oulu, Oulu University Hospital, University of Oulu, Aapistie 5A, 90220, Oulu, Finland.
Tero RautioTranslational Medicine Research Unit, Medical Research Center Oulu, Oulu University Hospital, University of Oulu, Aapistie 5A, 90220, Oulu, Finland.
Markus J MäkinenTranslational Medicine Research Unit, Medical Research Center Oulu, Oulu University Hospital, University of Oulu, Aapistie 5A, 90220, Oulu, Finland.
Juha P VäyrynenTranslational Medicine Research Unit, Medical Research Center Oulu, Oulu University Hospital, University of Oulu, Aapistie 5A, 90220, Oulu, Finland. juha.vayrynen@oulu.fi.ORCID http://orcid.org/0000-0002-8683-2996

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Local and systemic inflammation play key roles in colorectal cancer (CRC). Matrix metalloproteinase 8 (MMP8), an enzyme involved in extracellular matrix remodeling, has been linked to both inflammatory processes and cancer progression. This study investigates MMP8 serum concentration and MMP8 expression within the tumor microenvironment, and their relationship with tumor characteristics, inflammation, and survival. The study included 776 stage I-IV CRC patients. MMP8+ cell densities within tumors were analyzed using immunohistochemistry combined with digital image analysis, while preoperative serum MMP8 levels were analyzed using an immunofluorometric assay. Survival analyses were performed using the Kaplan-Meier method and Cox regression models. Correlations with systemic inflammatory markers and immune cell densities were assessed using linear regression models. We found that MMP8 was predominantly expressed by CEACAM8+ granulocytes. High MMP8+ cell density within tumors was associated with favorable prognostic factors, including low disease stage, absent lymphovascular invasion, and mismatch repair (MMR) deficiency, but also with improved cancer-specific survival independent of these factors. The multivariable HR for low (vs. high) MMP8+ cell density was 1.76 (95%CI 1.18–2.60). MMP8+ cell density positively correlated with T-cell densities, but not with serum MMP8 levels or conventional systemic inflammation markers. In contrast, high serum MMP8 levels were associated with systemic inflammation and worse survival, but did not remain an independent prognostic factor in multivariable models. In conclusion, serum MMP8 levels do not correlate with MMP8 expression in the tumor microenvironment, suggesting distinct roles for circulating and tumor-associated MMP8 in CRC progression. High MMP8+ cell densities within tumors are associated with better prognosis and local immune activity, while elevated serum MMP8 levels indicate systemic inflammation and advanced disease.

Indexed as

Biomarkers, TumorColorectal NeoplasmsMatrix Metalloproteinase 8AdultAgedAged, 80 and overFemaleHumansImmunohistochemistryMaleMiddle AgedPrognosisSurvival AnalysisTumor MicroenvironmentBiomarkers, TumorMatrix Metalloproteinase 8MMP8 protein, humanColorectal cancerImmune cellsMMP8Prognosis

Identifiers

PMID41931149
PMCPMC13199190

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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.