Tumor-associated nonmyelinating Schwann cell- expressed PVT1 promotes pancreatic cancer kynurenine pathway and tumor immune exclusion

One of the major obstacles to treating pancreatic ductal adenocarcinoma (PDAC) is its immunoresistant microenvironment. The functional importance and molecular mechanisms of Schwann cells in PDAC remains largely elusive. We characterized the gene signature of tumor-associated nonmyelinating Schwann cells (TASc) in PDAC and indicated that the abundance of TASc was correlated with immune suppressive tumor microenvironment and the unfavorable outcome of patients with PDAC. Depletion of pancreatic-specific TASc promoted the tumorigenesis of PDAC tumors. TASc-expressed long noncoding RNA (lncRNA) plasmacytoma variant translocation 1 (PVT1) was triggered by the tumor cell-produced interleukin-6. Mechanistically, PVT1 modulated RAF proto-oncogene serine/threonine protein kinase-mediated phosphorylation of tryptophan 2,3-dioxygenase in TASc, facilitating its enzymatic activities in catalysis of tryptophan to kynurenine. Depletion of TASc-expressed PVT1 suppressed PDAC tumor growth. Furthermore, depletion of TASc using a small-molecule inhibitor effectively sensitized PDAC to immunotherapy, signifying the important roles of TASc in PDAC immune resistance.

Automated summary

One major obstacle in treating PDAC is its immunoresistant microenvironment. This study identified the importance of Schwann cells in PDAC and their correlation with immune suppressive tumor microenvironment and poor patient outcomes. It was found that the depletion of pancreatic-specific TASc promoted PDAC tumor growth, while depletion of TASc-expressed PVT1 suppressed tumor growth and sensitized PDAC to immunotherapy. The findings highlight the significant roles of TASc in PDAC immune resistance.