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Evaluation of Biomarkers in Glioma by Immunohistochemistry on Paraffin-Embedded 3D Glioma Neurosphere Cultures
Published on: January 9, 2019
ELTD1, a potential new biomarker for gliomas
Rheal A Towner1, Randy L Jensen, Howard Colman
1Advanced Magnetic Resonance Center, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma 73104, USA. Rheal-Towner@omrf.org
Epidermal growth factor, latrophilin, and 7 transmembrane domain-containing protein 1 (ELTD1) is a promising new biomarker for glioma diagnosis. This study identified ELTD1 as significantly elevated in high-grade gliomas, validating its potential in both human and rodent models.
Area of Science:
- Oncology
- Biomarker Discovery
- Bioinformatics
Background:
- Glioblastoma multiforme (GBM) is an aggressive brain tumor with poor prognosis.
- Identifying novel biomarkers is crucial for improved GBM diagnosis and treatment.
- GBM is characterized by diffuse invasion, angiogenesis, and high malignancy.
Purpose of the Study:
- To identify epidermal growth factor, latrophilin, and 7 transmembrane domain-containing protein 1 (ELTD1) as a potential glioma-associated biomarker.
- Utilize bioinformatics and data mining for novel biomarker prediction.
- Validate ELTD1 as a diagnostic marker in glioma models.
Main Methods:
- Employed advanced data mining and bioinformatics to predict ELTD1.
- Validated ELTD1 levels using immunohistochemistry in human and rat gliomas.
- Assessed in vivo ELTD1 levels in rat gliomas via molecular magnetic resonance imaging.
Main Results:
- ELTD1 was significantly elevated in high-grade gliomas compared to low-grade gliomas (P = .03).
- ELTD1 expression correlated with glioma grade, survival, and mesenchymal subtype.
- Significantly high in vivo ELTD1 levels were detected in rat F98 gliomas (P < .001).
Conclusions:
- Bioinformatic analysis successfully identified ELTD1 as a putative glioma biomarker.
- ELTD1 detection was validated in both human and rodent glioma models.
- ELTD1 shows potential as an additional biomarker for glioma diagnosis in preclinical and clinical settings.
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