Myeloperoxidase Alters Lung Cancer Cell Function to Benefit Their Survival

Author:

Cosic-Mujkanovic Nejra1,Valadez-Cosmes Paulina1,Maitz Kathrin1ORCID,Lueger Anna1ORCID,Mihalic Zala N.1,Runtsch Marah C.1ORCID,Kienzl Melanie12,Davies Michael J.3ORCID,Chuang Christine Y.3ORCID,Heinemann Akos12ORCID,Schicho Rudolf12,Marsche Gunther12ORCID,Kargl Julia12ORCID

Affiliation:

1. Division of Pharmacology, Otto Loewi Research Center, Medical University of Graz, 8010 Graz, Austria

2. BioTechMed-Graz, 8010 Graz, Austria

3. Department of Biomedical Sciences, Panum Institute, University of Copenhagen, DK-2200 Copenhagen, Denmark

Abstract

Myeloperoxidase (MPO) is a neutrophil-derived enzyme that has been recently associated with tumour development. However, the mechanisms by which this enzyme exerts its functions remain unclear. In this study, we investigated whether myeloperoxidase can alter the function of A549 human lung cancer cells. We observed that MPO promoted the proliferation of cancer cells and inhibited their apoptosis. Additionally, it increased the phosphorylation of AKT and ERK. MPO was rapidly bound to and internalized by A549 cells, retaining its enzymatic activity. Furthermore, MPO partially translocated into the nucleus and was detected in the chromatin-enriched fraction. Effects of MPO on cancer cell function could be reduced when MPO uptake was blocked with heparin or upon inhibition of the enzymatic activity with the MPO inhibitor 4-aminobenzoic acid hydrazide (4-ABAH). Lastly, we have shown that tumour-bearing mice treated with 4-ABAH had reduced tumour burden when compared to control mice. Our results highlight the role of MPO as a neutrophil-derived enzyme that can alter the function of lung cancer cells.

Funder

Austrian Science Fund

BioTechMed Graz

Novo Nordisk Foundation

Publisher

MDPI AG

Subject

Cell Biology,Clinical Biochemistry,Molecular Biology,Biochemistry,Physiology

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