The extracellular matrix landscape in salivary gland carcinomas is defined by cellular differentiation via expression of three distinct protein modules

Author:

Arolt Christoph1ORCID,Hoffmann Franziska23,Nachtsheim Lisa4,Mayer Marcel4,Guntinas‐Lichius Orlando3,Buettner Reinhard1,von Eggeling Ferdinand35,Klussmann Jens Peter46,Hillmer Axel16ORCID,Quaas Alexander1,Klein Sebastian17ORCID,Wolber Philipp4

Affiliation:

1. Institute of Pathology, Medical Faculty University of Cologne Cologne Germany

2. Department of Otorhinolaryngology MALDI Imaging and Innovative Biophotonics, Jena University Hospital Jena Germany

3. Department of Otorhinolaryngology, Head and Neck Surgery Jena University Hospital Jena Germany

4. Department of Otorhinolaryngology, Head and Neck Surgery, Medical Faculty University of Cologne Cologne Germany

5. MALDI Imaging, Core Unit Proteome Analysis, DFG Core Unit Jena Biophotonic and Imaging, Laboratory (JBIL) Jena University Hospital Jena Germany

6. Center for Molecular Medicine Cologne (CMMC) University of Cologne Cologne Germany

7. Department of Hematology and Stem Cell Transplantation University Duisburg‐Essen, University Hospital Essen Essen Germany

Abstract

AbstractThe extracellular matrix (ECM) is an integral part of the tumor microenvironment of carcinomas. Even though salivary gland carcinomas (SGCs) display a range of tumor cell differentiation and distinct extracellular matrices, their ECM landscape has not been characterized in depth. The ECM composition of 89 SGC primaries, 14 metastases, and 25 normal salivary gland tissues was assessed using deep proteomic profiling. Machine learning algorithms and network analysis were used to detect tumor groups and protein modules that explain specific ECM landscapes. Multimodal in situ studies to validate exploratory findings and to infer a putative cellular origin of ECM components were applied. We revealed two fundamental SGC ECM classes which align with the presence or absence of myoepithelial tumor differentiation. We describe the SGC ECM through three biologically distinct protein modules that are differentially expressed across ECM classes and cell types. The modules have a distinct prognostic impact on different SGC types. Since targeted therapy is rarely available for SGC, we used the proteomic expression profile to identify putative therapeutic targets. In summary, we provide the first extensive inventory of ECM components in SGC, a difficult‐to‐treat disease that encompasses tumors with distinct cellular differentiation. © 2023 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.

Funder

Deutsche Forschungsgemeinschaft

Publisher

Wiley

Subject

Pathology and Forensic Medicine

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