Targeting Pediatric Glioblastomas by Combining OLIG2 Inhibitor CT-179 with Fractionated Radiation in a Panel of Patient-Derived Orthotopic Xenograft Mouse Models
The poor clinical outcomes of pediatric high-grade glioma (pHGG) highlight the urgent need for new therapies. Oligodendrocyte lineage transcription factor 2 (<i>OLIG2</i>) is a pro-mitotic transcription factor highly expressed in glioma stem cells and may represent a novel therapeutic target. To evaluate the therapeutic efficacy of an <i>OLIG2</i> inhibitor CT-179 in pHGG, we determined the <i>OLIG2</i> mRNA expression in 10 patient-derived orthotopic xenograft (PDOX) models. In vitro activities of CT-179 were analyzed in monolayer and neurosphere cells (0-10 µM) with and without radiation (XRT) (0-8 Gy), brain penetration was evaluated in tumor-bearing PDOX mice, and in vivo efficacy was determined at 15-240 mg/kg (oral) alone or combined with XRT (2 Gy/day × 5 days). Changes in animal survival times were analyzed using the Kaplan-Meier method, followed by pair-wise comparisons. Increased <i>OLIG2</i> mRNA expression was detected in seven out of ten PDOX models. CT-179 inhibited cell viability in a time- and dose-dependent manner in all eight pGBM xenograft tumors (IC<sub>50</sub> 0.03-10 µM) and was potentiated by XRT (0.03-1 µM). Oral gavage (24 mg/kg) of CT-179 for 5 days led to effective penetration in mouse cerebrum (3232.7 ± 569.2 ng/g), cerebellum (1563.3 ± 269.6 ng/g), brain stem (1685.3 ± 309 ng/g), and PDOX tumors (1814 ± 110.3 ng/g) vs. 361.3 ± 1.5 ng/mL in serum. CT-179 alone was not active at 200 mg/kg in four models, although it was moderately effective at 240 mg/kg in one model. When combined with XRT, a significant extension of animal survival times was observed in two out of four models. Doses needed to eliminate OLIG2 expression in vitro varied from 0.3 to >1 µM in pGBM cells. In summary, our data showed that orally administered CT-179 penetrated the blood-brain barrier (BBB) and exhibited potential for inhibiting pGBM growth when combined with XRT.
Authors
- Steve Neuhauser
- Emily L. Jocoy (ORCID: https://orcid.org/0000-0002-1583-8020)
- Graham Beaton (ORCID: https://orcid.org/0000-0001-6937-4121)
- X. Li
- Gregory Stein (ORCID: https://orcid.org/0000-0002-3588-8834)
- Jeff Chuang
- Malcolm A. Smith (ORCID: https://orcid.org/0000-0001-9880-9876)
- Carol J. Bult
- Frank Braun (ORCID: https://orcid.org/0000-0002-5514-1412)
- Clifford Stephan (ORCID: https://orcid.org/0000-0003-0657-6484)
- Gordon Alton (ORCID: https://orcid.org/0000-0002-2521-1336)
- S Zhao
- Yuchen Du
- Huiyuan Zhang
- Beverly Teicher
- Tim Stearns
- Holly Lindsay
- Santosh Kesari
- Mari Kogiso
- Lin Qi
Institutions
- Northwestern University (US)
- Lurie Children's Hospital (US)
- Guilin Medical University (CN)
- Baylor College of Medicine (US)
- Cook Children's Medical Center (US)
- Children's Hospital Colorado (US)
- Saint John's Health Center (US)
- Texas A&M Health Science Center (US)
- Center for Cancer and Blood Disorders (US)
- Jackson Laboratory (US)
- Arena Pharmaceuticals (United States) (US)
- National Cancer Institute (US)
- Texas Children's Hospital (US)
- Children's Cancer Center (US)
- The University of Texas Health Science Center (US)
- Ludwig-Maximilians-Universität München (DE)
- The University of Texas Health Science Center at Houston (US)
- University of Colorado Denver (US)
Publication Details
- Journal
- International Journal of Molecular Sciences
- Published
- 2026-02-04
- DOI
- https://doi.org/10.3390/ijms27031543
- Primary Topic
- Glioma Diagnosis and Treatment
- Type
- article
- Field-Weighted Citation Impact
- 0.00