Matrix Metalloproteinase 8 Expression in a Tumour Predicts a Favourable Prognosis in Pancreatic Ductal Adenocarcinoma.


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
18 Mar 2022
Historique:
received: 29 12 2021
revised: 07 03 2022
accepted: 10 03 2022
entrez: 25 3 2022
pubmed: 26 3 2022
medline: 9 4 2022
Statut: epublish

Résumé

Pancreatic ductal adenocarcinoma (PDAC) is a significant cause of cancer-related death globally, and, despite improvements in diagnostics and treatment, survival remains poor. Matrix metalloproteinases (MMPs) are enzymes involved in stroma remodelling in inflammation and cancer. MMP-8 plays a varied prognostic role in cancers of the gastrointestinal tract. We examined the prognostic value of MMP-8 immunoexpression in tumour tissue and the amount of MMP-8-positive polymorphonuclear cells (PMNs) in PDAC and their association with immune responses using C-reactive protein (CRP) as a marker of systemic inflammation. Tumour samples from 141 PDAC patients undergoing surgery in 2002−2011 at the Department of Surgery, Helsinki University Hospital were stained immunohistochemically, for which we evaluated MMP-8 expression in cancer cells and the amount of MMP-8-positive PMNs. We assessed survival using the Kaplan−Meier analysis while uni- and multivariable analyses relied on the Cox proportional hazards model. A negative MMP-8 stain and elevated CRP level predicted a poor prognosis (hazard ratio [HR] = 6.95; 95% confidence interval (CI) 2.69−17.93; p < 0.001) compared to a positive stain and low CRP level (<10 mg/L). The absence of PMNs together with an elevated CRP level also predicted an unfavourable outcome (HR = 3.17; 95% CI 1.60−6.30; p = 0.001). MMP-8 expression in the tumour served as an independent positive prognostic factor (HR = 0.33; 95% CI 0.16−0.68; p = 0.003). Tumour MMP-8 expression and a low CRP level may predict a favourable outcome in PDAC with similar results for MMP-8-positive PMNs and low CRP levels. Tumoural MMP-8 expression represents an independent positive prognostic factor in PDAC.

Identifiants

pubmed: 35328734
pii: ijms23063314
doi: 10.3390/ijms23063314
pmc: PMC8951094
pii:
doi:

Substances chimiques

Biomarkers, Tumor 0
MMP8 protein, human EC 3.4.24.34
Matrix Metalloproteinase 8 EC 3.4.24.34

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Mirjami Kaasinen (M)

Department of Surgery, University of Helsinki and Helsinki University Hospital, 00290 Helsinki, Finland.

Jaana Hagström (J)

Department of Pathology, University of Helsinki and Helsinki University Hospital, 00290 Helsinki, Finland.
Department of Oral Pathology and Radiology, University of Turku, 20014 Turku, Finland.
Translational Cancer Medicine Research Programme, Faculty of Medicine, University of Helsinki, 00290 Helsinki, Finland.

Harri Mustonen (H)

Department of Surgery, University of Helsinki and Helsinki University Hospital, 00290 Helsinki, Finland.
Translational Cancer Medicine Research Programme, Faculty of Medicine, University of Helsinki, 00290 Helsinki, Finland.

Timo Sorsa (T)

Department of Oral and Maxillofacial Diseases, University of Helsinki and Helsinki University Hospital, 00290 Helsinki, Finland.
Section of Periodontology and Dental Prevention, Division of Oral Diseases, Department of Dental Medicine, Karolinska Institutet, 17177 Solna, Sweden.

Malin Sund (M)

Department of Surgery, University of Helsinki and Helsinki University Hospital, 00290 Helsinki, Finland.
Department of Surgery and Perioperative Sciences/Surgery, Umeå University, 90187 Umeå, Sweden.

Caj Haglund (C)

Department of Surgery, University of Helsinki and Helsinki University Hospital, 00290 Helsinki, Finland.
Translational Cancer Medicine Research Programme, Faculty of Medicine, University of Helsinki, 00290 Helsinki, Finland.

Hanna Seppänen (H)

Department of Surgery, University of Helsinki and Helsinki University Hospital, 00290 Helsinki, Finland.
Translational Cancer Medicine Research Programme, Faculty of Medicine, University of Helsinki, 00290 Helsinki, Finland.

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Classifications MeSH