1. Academic Validation
  2. Modeling synovial sarcoma metastasis in the mouse: PI3'-lipid signaling and inflammation

Modeling synovial sarcoma metastasis in the mouse: PI3'-lipid signaling and inflammation

  • J Exp Med. 2016 Dec 12;213(13):2989-3005. doi: 10.1084/jem.20160817.
Jared J Barrott 1 2 3 Lisa A Kafchinski 1 Huifeng Jin 1 2 3 Jared W Potter 1 2 3 Sarmishta D Kannan 1 2 3 Robert Kennedy 1 2 3 Tim Mosbruger 3 4 Wei-Lien Wang 5 Jen-Wei Tsai 5 Dejka M Araujo 6 Ting Liu 3 7 Mario R Capecchi 8 Alexander J Lazar 5 Kevin B Jones 9 2 3
Affiliations

Affiliations

  • 1 Department of Orthopaedics, University of Utah, Salt Lake City, UT 84112.
  • 2 Department of Oncological Sciences, University of Utah, Salt Lake City, UT 84112.
  • 3 Huntsman Cancer Institute, University of Utah, Salt Lake City, UT 84112.
  • 4 Department of Bioinformatics, University of Utah, Salt Lake City, UT 84112.
  • 5 Departments of Pathology and Translational Molecular Pathology, M.D. Anderson Cancer Center, Houston, TX 77030.
  • 6 Sarcoma Medical Oncology, M.D. Anderson Cancer Center, Houston, TX 77030.
  • 7 Department of Pathology, University of Utah, Salt Lake City, UT 84112.
  • 8 Department of Human Genetics, University of Utah, Salt Lake City, UT 84112.
  • 9 Department of Orthopaedics, University of Utah, Salt Lake City, UT 84112 kevin.jones@hci.utah.edu.
Abstract

Solid tumor metastasis is a complex biology, impinged upon by a variety of dysregulated signaling pathways. PI3'-lipid signaling has been associated with metastasis and inflammation in many cancers, but the relationship between tumor cell-intrinsic PI3'-lipid signaling and inflammatory cell recruitment has remained enigmatic. Elevated PI3'-lipid signaling associates with progression of synovial sarcoma, a deadly soft tissue malignancy initiated by a t(X;18) chromosomal translocation that generates an SS18-SSX fusion oncoprotein. Here, we show in genetically engineered mouse models of locally induced expression of SS18-SSX1 or SS18-SSX2 that PTEN silencing dramatically accelerated and enhanced sarcomagenesis without compromising synovial sarcoma characteristics. PTEN deficiency increased tumor angiogenesis, promoted inflammatory gene expression, and enabled highly penetrant spontaneous pulmonary metastasis. PTEN-deficient sarcomas revealed infiltrating myeloid-derived hematopoietic cells, particularly macrophages and neutrophils, recruited via PI3'-lipid-induced CSF1 expression in tumor cells. Moreover, in a large panel of human synovial sarcomas, enhanced PI3'-lipid signaling also correlated with increased inflammatory cell recruitment and CSF1R signal transduction in both macrophages and endothelial cells. Thus, both in the mouse model and in human synovial sarcomas, PI3'-lipid signaling drives CSF1 expression and associates with increased infiltration of the monocyte/macrophage lineage as well as neutrophils.

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