Endosialin (CD248) Cancer Role and Therapeutics: 33 years on
Since its discovery more than 30 years ago, our understanding of the function of CD248 (also known as endosialin or TEM1) as a therapeutic target has evolved, and CD248 is now recognized as a potentially valuable target for therapeutics directed toward sarcomas and fibrotic diseases. The current study reviews the literature related to CD248 and examines CD248 expression across various models including patient-derived xenografts, patient-derived cell lines (pdmr.cancer.gov/), and large cell line collections, including the Cell Line Encyclopedia (CCLE) and the GDSC-MGH-Sanger. CD248 is highly and selectively expressed by sarcomas and by pericytes in tumor vasculature and wound-healing vasculature. It is a component of a multi-protein complex which connects various cell types into tissue structure. Multiple therapeutic approaches are being investigated to take advantage of CD248 in the treatment of sarcomas and fibrotic diseases. Endosialin/CD248/TEM1 is a promising biological target that remains poorly explored in cancer therapy. Importantly, CD248 is overexpressed in several human solid tumors and absent in most normal adult tissues, making it a suitable and potentially safe target for radioimmunotherapy, particularly in Ewing's sarcoma xenograft models.
Authors
- Dianne L. Newton
- Nathan P. Coussens (ORCID: https://orcid.org/0000-0002-3896-7909)
- Thomas Steven Dexheimer (ORCID: https://orcid.org/0000-0002-6444-3121)
- Melinda G. Hollingshead (ORCID: https://orcid.org/0000-0002-1207-1397)
- Li Chen
- Beverly A. Teicher
- James H. Doroshow
Institutions
- Leidos (United States) (US)
- Frederick National Laboratory for Cancer Research (US)
- National Cancer Institute (MY)
- National Cancer Institute (US)
Publication Details
- Journal
- Molecular Cancer Therapeutics
- Published
- 2026-02-19
- DOI
- https://doi.org/10.1158/1535-7163.mct-25-0759
- Primary Topic
- Hippo pathway signaling and YAP/TAZ
- Type
- article
- Field-Weighted Citation Impact
- 0.00