| First Author | Li Y | Year | 2024 |
| Journal | Cancer Sci | Volume | 115 |
| Issue | 2 | Pages | 401-411 |
| PubMed ID | 38041233 | Mgi Jnum | J:346522 |
| Mgi Id | MGI:7616659 | Doi | 10.1111/cas.16037 |
| Citation | Li Y, et al. (2024) TGF-beta signaling promotes desmoid tumor formation via CSRP2 upregulation. Cancer Sci 115(2):401-411 |
| abstractText | Desmoid tumors (DTs), also called desmoid-type fibromatoses, are locally aggressive tumors of mesenchymal origin. In the present study, we developed a novel mouse model of DTs by inducing a local mutation in the Ctnnb1 gene, encoding beta-catenin in PDGFRA-positive stromal cells, by subcutaneous injection of 4-hydroxy-tamoxifen. Tumors in this model resembled histologically clinical samples from DT patients and showed strong phosphorylation of nuclear SMAD2. Knockout of SMAD4 in the model significantly suppressed tumor growth. Proteomic analysis revealed that SMAD4 knockout reduced the level of Cysteine-and-Glycine-Rich Protein 2 (CSRP2) in DTs, and treatment of DT-derived cells with a TGF-beta receptor inhibitor reduced CSRP2 RNA levels. Knockdown of CSRP2 in DT cells significantly suppressed their proliferation. These results indicate that the TGF-beta/CSRP2 axis is a potential therapeutic target for DTs downstream of TGF-beta signaling. |
