MDA-9/Syntenin in the tumor and microenvironment defines prostate cancer bone metastasis

Author:

Maji Santanu1ORCID,Pradhan Anjan K.12,Kumar Amit1,Bhoopathi Praveen12,Mannangatti Padmanabhan12,Guo Chunqing123ORCID,Windle Jolene J.123,Subler Mark A.12,Wang Xiang-Yang123,Semmes Oliver J.4ORCID,Nyalwidhe Julius O.4,Mukhopadhyay Nitai35,Paul Asit Kr.36,Hatfield Bryce7,Levit Michael M.8,Madan Esha239,Sarkar Devanand123,Emdad Luni123,Cohen David J.8,Gogna Rajan123,Cavenee Webster K.10ORCID,Das Swadesh K.123ORCID,Fisher Paul B.123

Affiliation:

1. Department of Human and Molecular Genetics, Virginia Commonwealth University, School of Medicine, Richmond, VA 23298

2. VCU Institute of Molecular Medicine, Virginia Commonwealth University, School of Medicine, Richmond, VA 23298

3. VCU Massey Comprehensive Cancer Center, Virginia Commonwealth University, School of Medicine, Richmond, VA 23298

4. Department of Microbiology and Molecular Cell Biology, Eastern Virginia Medical School, Norfolk, VA 23507

5. Department of Biostatistics, Virginia Commonwealth University, School of Medicine, Richmond, VA 23238

6. Department of Internal Medicine, Virginia Commonwealth University, School of Medicine, Richmond, VA 23238

7. Department of Pathology, Virginia Commonwealth University, School of Medicine, Richmond, VA 23238

8. Department of Biomedical Engineering, College of Engineering, Virginia Commonwealth University, Richmond, VA 23238

9. Department of Surgery, Virginia Commonwealth University, School of Medicine, Richmond, VA 23238

10. Ludwig Institute for Cancer Research, University of California San Diego, La Jolla, CA 92093

Abstract

Bone metastasis is a frequent and incurable consequence of advanced prostate cancer (PC). An interplay between disseminated tumor cells and heterogeneous bone resident cells in the metastatic niche initiates this process. Melanoma differentiation associated gene-9 ( mda-9/Syntenin/syndecan binding protein ) is a prometastatic gene expressed in multiple organs, including bone marrow–derived mesenchymal stromal cells (BM-MSCs), under both physiological and pathological conditions. We demonstrate that PDGF-AA secreted by tumor cells induces CXCL5 expression in BM-MSCs by suppressing MDA-9-dependent YAP/MST signaling. CXCL5-derived tumor cell proliferation and immune suppression are consequences of the MDA-9/CXCL5 signaling axis, promoting PC disease progression. mda-9 knockout tumor cells express less PDGF-AA and do not develop bone metastases. Our data document a previously undefined role of MDA-9/Syntenin in the tumor and microenvironment in regulating PC bone metastasis. This study provides a framework for translational strategies to ameliorate health complications and morbidity associated with advanced PC.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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