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

Institutions

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
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Endosialin (CD248) Cancer Role and Therapeutics: 33 years on

Dianne L. Newton, Nathan P. Coussens, Thomas Steven Dexheimer, Melinda G. Hollingshead et al.
Molecular Cancer Therapeutics
Hippo pathway signaling and YAP/TAZ
article

Endosialin (CD248) Cancer Role and Therapeutics: 33 years on

Dianne L. Newton, Nathan P. Coussens, Thomas Steven Dexheimer, Melinda G. Hollingshead, Li Chen, Beverly A. Teicher, James H. Doroshow
article en

Abstract

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.

Molecular Cancer Therapeutics
Leidos (United States) (US), Frederick National Laboratory for Cancer Research (US), National Cancer Institute (MY), National Cancer Institute (US)
Good health and well-being
Openalex Percentile: Top 53%
Hippo pathway signaling and YAP/TAZ
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Endosialin (CD248) Cancer Role and Therapeutics: 33 years on — Dianne L. Newton, Nathan P. Coussens, et al. · Molecular Cancer Therapeutics (2026) | TGRS Research Map | TGRS