Enhancing the efficacy of VEGF inhibitors by co-inhibition of HIF in the treatment of glioblastoma

Glioblastoma is the most aggressive and most common grade 4 tumor of the central nervous system (CNS). Despite standard treatments such as surgical resection and chemoradiotherapy, overall survival (OS) usually does not exceed 14-16 months in clinical trials, and no improvement in OS has been demonstrated even with the use of vascular endothelial growth factor A (VEGFA) inhibitors such as bevacizumab. In response to radiotherapy, hypoxia-inducible factor (HIF) stabilization leads to activation of alternative pro-angiogenic pathways, increasing VEGF expression and tumor angiogenesis. Several clinical trials evaluating HIF-2α inhibitors as monotherapy in the absence of concurrent VEGF inhibition, have similarly failed to demonstrate a significant improvement in OS outcomes. This review provides a perspective on the combined use of VEGF and HIF inhibitors, and provides an insight into future studies.

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Journal
APOPTOSIS
Published
2026-01-23
DOI
https://doi.org/10.1007/s10495-026-02275-5
Primary Topic
Cancer, Hypoxia, and Metabolism
Type
article
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article

Enhancing the efficacy of VEGF inhibitors by co-inhibition of HIF in the treatment of glioblastoma

Oral Oncul, Didem Taştekin, Murat Faik Erdoğan, Abdul Kadir Slocum et al.
APOPTOSIS
Cancer, Hypoxia, and Metabolism
article

Enhancing the efficacy of VEGF inhibitors by co-inhibition of HIF in the treatment of glioblastoma

Oral Oncul, Didem Taştekin, Murat Faik Erdoğan, Abdul Kadir Slocum, Emirhan Harbi, Hamza Uğur Bozbey, Duha Yahya, Christopher E. Mason, Michael Aschner, Ozcan Yildiz, Soha Hosseiny, Yasemin Yozgat Byrne
article en

Abstract

Glioblastoma is the most aggressive and most common grade 4 tumor of the central nervous system (CNS). Despite standard treatments such as surgical resection and chemoradiotherapy, overall survival (OS) usually does not exceed 14-16 months in clinical trials, and no improvement in OS has been demonstrated even with the use of vascular endothelial growth factor A (VEGFA) inhibitors such as bevacizumab. In response to radiotherapy, hypoxia-inducible factor (HIF) stabilization leads to activation of alternative pro-angiogenic pathways, increasing VEGF expression and tumor angiogenesis. Several clinical trials evaluating HIF-2α inhibitors as monotherapy in the absence of concurrent VEGF inhibition, have similarly failed to demonstrate a significant improvement in OS outcomes. This review provides a perspective on the combined use of VEGF and HIF inhibitors, and provides an insight into future studies.

APOPTOSISVol. 31(2)
Üsküdar University (TR), Bahçeşehir University (TR), Albert Einstein College of Medicine (US), Cornell University (US), Ondokuz Mayıs University (TR), Istanbul Medipol University (TR), Biruni University (TR), Istanbul Metropolitan Municipality (TR), Weill Cornell Medicine (US), İstanbul Başakşehir Çam ve Sakura Şehir Hastanesi, Istanbul University (TR)
Good health and well-being
Openalex Percentile: Top 81%
Cancer, Hypoxia, and Metabolism
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