| First Author | Moritsch S | Year | 2022 |
| Journal | Oncoimmunology | Volume | 11 |
| Issue | 1 | Pages | 2127271 |
| PubMed ID | 36185806 | Mgi Jnum | J:333919 |
| Mgi Id | MGI:7443283 | Doi | 10.1080/2162402X.2022.2127271 |
| Citation | Moritsch S, et al. (2022) Tyk2 is a tumor suppressor in colorectal cancer. Oncoimmunology 11(1):2127271 |
| abstractText | Janus kinase Tyk2 is implicated in cancer immune surveillance, but its role in solid tumors is not well defined. We used Tyk2 knockout mice (Tyk2(Delta/Delta)) and mice with conditional deletion of Tyk2 in hematopoietic (Tyk2(DeltaHem)) or intestinal epithelial cells (Tyk2(DeltaIEC)) to assess their cell type-specific functions in chemically induced colorectal cancer. All Tyk2-deficient mouse models showed a higher tumor burden after AOM-DSS treatment compared to their corresponding wild-type controls (Tyk2(+/+) and Tyk2(fl/fl)), demonstrating tumor-suppressive functions of Tyk2 in immune cells and epithelial cancer cells. However, specific deletion of Tyk2 in hematopoietic cells or in intestinal epithelial cells was insufficient to accelerate tumor progression, while deletion in both compartments promoted carcinoma formation. RNA-seq and proteomics revealed that tumors of Tyk2(Delta/Delta) and Tyk2(DeltaIEC) mice were immunoedited in different ways with downregulated and upregulated IFNgamma signatures, respectively. Accordingly, the IFNgamma-regulated immune checkpoint Ido1 was downregulated in Tyk2(Delta/Delta) and upregulated in Tyk2(DeltaIEC) tumors, although both showed reduced CD8(+) T cell infiltration. These data suggest that Tyk2(Delta/Delta) tumors are Ido1-independent and poorly immunoedited while Tyk2(DeltaIEC) tumors require Ido1 for immune evasion. Our study shows that Tyk2 prevents Ido1 expression in CRC cells and promotes CRC immune surveillance in the tumor stroma. Both of these Tyk2-dependent mechanisms must work together to prevent CRC progression. |
