Bovine meat and milk factor protein expression in tumor‐free mucosa of colorectal cancer patients coincides with macrophages and might interfere with patient survival

Author:

Nikitina Ekaterina1,Burk‐Körner Amelie1,Wiesenfarth Manuel2,Alwers Elizabeth3,Heide Danijela4,Tessmer Claudia5,Ernst Claudia1,Krunic Damir6,Schrotz‐King Petra7,Chang‐Claude Jenny89,von Winterfeld Moritz1011,Herpel Esther1012,Brobeil Alexander1012,Brenner Hermann3713,Heikenwalder Mathias4,Hoffmeister Michael3,Kopp‐Schneider Annette2,Bund Timo1ORCID

Affiliation:

1. Division of Episomal‐persistent DNA in Cancer‐ and Chronic Diseases German Cancer Research Center (DKFZ) Heidelberg Germany

2. Division of Biostatistics German Cancer Research Center (DKFZ) Heidelberg Germany

3. Division of Clinical Epidemiology and Aging Research German Cancer Research Center (DKFZ) Heidelberg Germany

4. Division of Chronic Inflammation and Cancer German Cancer Research Center (DKFZ) Heidelberg Germany

5. Monoclonal Antibody Unit of the Genomics and Proteomics Core Facility German Cancer Research Center (DKFZ) Heidelberg Germany

6. Light Microscopy Facility German Cancer Research Center (DKFZ) Heidelberg Germany

7. Division of Preventive Oncology German Cancer Research Center (DKFZ) and National Center for Tumor Diseases (NCT) Heidelberg Germany

8. Unit of Genetic Epidemiology German Cancer Research Center (DKFZ) Heidelberg Germany

9. Cancer Epidemiology Group, University Medical Center Hamburg‐Eppendorf University Cancer Center Hamburg Hamburg Germany

10. Institute of Pathology University Hospital Heidelberg Germany

11. Pathologie Rosenheim Germany

12. Tissue Bank of the National Center for Tumor Diseases (NCT) Heidelberg Germany

13. German Cancer Consortium German Cancer Research Center Heidelberg Germany

Abstract

Bovine milk and meat factors (BMMFs) are plasmid‐like DNA molecules isolated from bovine milk and serum, as well as the peritumor of colorectal cancer (CRC) patients. BMMFs have been proposed as zoonotic infectious agents and drivers of indirect carcinogenesis of CRC, inducing chronic tissue inflammation, radical formation and increased levels of DNA damage. Data on expression of BMMFs in large clinical cohorts to test an association with co‐markers and clinical parameters were not previously available and were therefore assessed in this study. Tissue sections with paired tumor‐adjacent mucosa and tumor tissues of CRC patients [individual cohorts and tissue microarrays (TMAs) (n = 246)], low‐/high‐grade dysplasia (LGD/HGD) and mucosa of healthy donors were used for immunohistochemical quantification of the expression of BMMF replication protein (Rep) and CD68/CD163 (macrophages) by co‐immunofluorescence microscopy and immunohistochemical scoring (TMA). Rep was expressed in the tumor‐adjacent mucosa of 99% of CRC patients (TMA), was histologically associated with CD68+/CD163+ macrophages and was increased in CRC patients when compared to healthy controls. Tumor tissues showed only low stromal Rep expression. Rep was expressed in LGD and less in HGD but was strongly expressed in LGD/HGD‐adjacent tissues. Albeit not reaching statistical significance, incidence curves for CRC‐specific death were increased for higher Rep expression (TMA), with high tumor‐adjacent Rep expression being linked to the highest incidence of death. BMMF Rep expression might represent a marker and early risk factor for CRC. The correlation between Rep and CD68 expression supports a previous hypothesis that BMMF‐specific inflammatory regulations, including macrophages, are involved in the pathogenesis of CRC.

Funder

Bundesministerium für Bildung und Forschung

Deutsche Forschungsgemeinschaft

H2020 European Research Council

National Cancer Institute

Publisher

Wiley

Subject

Cancer Research,Genetics,Molecular Medicine,General Medicine,Oncology

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