The CAM Model for CIC-DUX4 Sarcoma and Its Potential Use for Precision Medicine

Cells. 2021 Oct 1;10(10):2613. doi: 10.3390/cells10102613.

Abstract

(1) Background: CIC-DUX4 sarcoma is a rare mesenchymal small round cell tumor which belongs to rare cancers that occupy a significant percentage of cancer cases as a whole, despite each being rare. Importantly, each rare cancer type has different features, and thus there is a need to develop a model that mimics the features of each of these cancers. We evaluated the idea that the chicken chorioallantoic membrane assay (CAM), a convenient and versatile animal model, can be established for the CIC-DUX4 sarcoma. (2) Methods: Patient-derived cell lines of CIC-DUX4 were applied. These cells were transplanted onto the CAM membrane and tumor formation was examined by H&E staining, immunohistochemistry and Western blotting. The CAM tumor was transferred onto a fresh CAM and was also used to form organoids. Retention of the fusion gene was examined. (3) Results: H&E staining as well as molecular characterization demonstrated the formation of the CIC-DUX4 tumor on the CAM membrane. Expression of cyclin D2 and ETV4 was identified. The CAM tumor was transferred to a fresh CAM to form the second-generation CAM tumor. In addition, we were successful in forming tumor organoids using the CAM tumor. Retention of the fusion gene CIC-DUX4 in the CAM, second-generation CAM, and in the CAM-derived organoids was confirmed by RT-PCR. (4) Conclusions: The CAM assay provides a promising model for CIC-DUX4 sarcoma.

Keywords: CAM assay; CIC-DUX4 sarcoma; H&E staining; fusion gene; organoids; rare cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers, Tumor / metabolism
  • Cell Line, Tumor
  • Chorioallantoic Membrane* / metabolism
  • Chorioallantoic Membrane* / pathology
  • Homeodomain Proteins / metabolism*
  • Humans
  • Oncogene Proteins, Fusion / metabolism*
  • Repressor Proteins / metabolism*
  • Sarcoma / metabolism*

Substances

  • Biomarkers, Tumor
  • CIC protein, human
  • DUX4L1 protein, human
  • Homeodomain Proteins
  • Oncogene Proteins, Fusion
  • Repressor Proteins