Short-term topiramate treatment prevents radiation-induced cytotoxic edema in preclinical models of breast-cancer brain metastasis

Author:

Contreras-Zárate Maria J1ORCID,Alvarez-Eraso Karen L F1,Jaramillo-Gómez Jenny A1,Littrell Zachary1,Tsuji Nikki2,Ormond D Ryan3,Karam Sana D4,Kabos Peter5,Cittelly Diana M1ORCID

Affiliation:

1. Department of Pathology, University of Colorado Anschutz Medical Campus , Aurora, Colorado , USA

2. Office of Laboratory Animal Resources, University of Colorado Anschutz Medical Campus , Aurora, Colorado , USA

3. Department of Neurosurgery, University of Colorado Anschutz Medical Campus , Aurora, Colorado , USA

4. Department of Radiation Oncology, University of Colorado Anschutz Medical Campus , Aurora, Colorado , USA

5. Department of Medicine, Division of Medical Oncology, University of Colorado Anschutz Medical Campus , Aurora, Colorado , USA

Abstract

Abstract Background Brain edema is a common complication of brain metastases (BM) and associated treatment. The extent to which cytotoxic edema, the first step in the sequence that leads to ionic edema, vasogenic edema, and brain swelling, contributes to radiation-induced brain edema during BM remains unknown. This study aimed to determine whether radiation-associated treatment of BM induces cytotoxic edema and the consequences of blocking the edema in preclinical models of breast-cancer brain metastases (BCBM). Methods Using in vitro and in vivo models, we measured astrocytic swelling, trans-electric resistance (TEER), and aquaporin 4 (AQP4) expression following radiation. Genetic and pharmacological inhibition of AQP4 in astrocytes and cancer cells was used to assess the role of AQP4 in astrocytic swelling and brain water intake. An anti-epileptic drug that blocks AQP4 function (topiramate) was used to prevent cytotoxic edema in models of BM. Results Radiation-induced astrocytic swelling and transient upregulation of AQP4 occurred within the first 24 hours following radiation. Topiramate decreased radiation-induced astrocytic swelling and loss of TEER in astrocytes in vitro, and acute short-term treatment (but not continuous administration), prevented radiation-induced increase in brain water content without pro-tumorigenic effects in multiple preclinical models of BCBM. AQP4 was expressed in clinical BM and breast-cancer cell lines, but AQP4 targeting had limited direct pro-tumorigenic or radioprotective effects in cancer cells that could impact its clinical translation. Conclusions Patients with BM could find additional benefits from acute and temporary preventive treatment of radiation-induced cytotoxic edema using anti-epileptic drugs able to block AQP4 function.

Funder

National Cancer Institute

National Institutes of Health

National Institute of Dental and Craniofacial Research

Clinical and Translational Science Awards

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Neurology (clinical),Oncology

Reference39 articles.

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