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短期托吡酯治疗可预防乳腺癌脑转移临床前模型中辐射诱导的细胞毒性水肿。

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

作者信息

Contreras-Zárate Maria J, Alvarez-Eraso Karen Lf, Jaramillo-Gómez Jenny A, Littrell Zachary, Tsuji Niki, Ormond David R, Karam Sana D, Kabos Peter, Cittelly Diana M

出版信息

bioRxiv. 2023 Feb 15:2023.02.14.528559. doi: 10.1101/2023.02.14.528559.

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 pre-clinical models of breast cancer brain metastases (BCBM).

METHODS

Using and 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 within the first 24 hours following radiation. Topiramate decreased radiation-induced astrocytic swelling, loss of TEER in astrocytes , and acute short term treatment (but not continuous administration), prevented radiation-induced increase in brain water content without pro-tumorigenic effects in multiple pre-clinical 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.

KEY POINTS

Radiation induces cytotoxic edema via acute dysregulation of AQP4 in astrocytes in preclinical models of BM. Pharmacologic blockage of AQP4 function prevents water intake, astrocytic swelling and restores TEER Pre-treatment with single-dose Topiramate prevents brain radiation-induced brain edema without direct tumor effects in pre-clinical models of BCBM.

IMPORTANCE OF THE STUDY

In this study we describe a novel role for astrocytic swelling and cytotoxic edema in the progression of radiation-induced brain edema during BM treatment. While radiation-induced edema has been fully attributed to the disruption of the blood-brain barrier (BBB) and ensuing vasogenic effects, our results suggest that cytotoxic edema affecting astrocytes in the acute setting plays an important role in the progression of brain edema during BM standard of care. Current standard of care for brain edema involves pre-treatment with steroids and the use of bevacizumab only after clinically significant edema develops. Both interventions are presumed to target vasogenic edema. This study suggests that patients with BM could find additional benefits from acute and temporary preventive treatment of radiation-induced cytotoxic edema using an already FDA-approved anti-epileptic drug. Such early prevention strategy can be easily clinically implemented with the goal of minimizing treatment-related toxicities.

摘要

背景

脑水肿是脑转移瘤(BM)及相关治疗的常见并发症。细胞毒性水肿作为导致离子性水肿、血管源性水肿和脑肿胀这一过程的第一步,在BM放疗期间对放射性脑水肿的影响程度尚不清楚。本研究旨在确定BM的放射相关治疗是否会诱导细胞毒性水肿,以及在乳腺癌脑转移(BCBM)的临床前模型中阻断水肿的后果。

方法

使用[具体模型1]和[具体模型2]模型,我们测量了放疗后星形胶质细胞肿胀、跨上皮电阻(TEER)和水通道蛋白4(AQP4)的表达。通过对星形胶质细胞和癌细胞中AQP4进行基因和药物抑制,来评估AQP4在星形胶质细胞肿胀和脑水摄取中的作用。一种阻断AQP4功能的抗癫痫药物(托吡酯)被用于预防BM模型中的细胞毒性水肿。

结果

放疗后24小时内可诱导星形胶质细胞肿胀并使AQP4短暂上调。托吡酯可减轻放疗诱导的星形胶质细胞肿胀、星形胶质细胞中TEER的丧失,并且在多个BCBM临床前模型中,急性短期治疗(而非持续给药)可预防放疗诱导的脑含水量增加且无促肿瘤作用。AQP4在临床BM和乳腺癌细胞系中表达,但靶向AQP4对癌细胞的直接促肿瘤或放射保护作用有限,这可能会影响其临床转化。

结论

BM患者使用能够阻断AQP4功能的抗癫痫药物对放射性诱导的细胞毒性水肿进行急性和临时预防性治疗可能会有额外益处。

关键点

在BM临床前模型中,放疗通过急性失调星形胶质细胞中的AQP4诱导细胞毒性水肿。对AQP4功能的药物阻断可防止水摄取、星形胶质细胞肿胀并恢复TEER。在BCBM临床前模型中,单剂量托吡酯预处理可预防脑放疗诱导的脑水肿且无直接肿瘤效应。

研究的重要性

在本研究中,我们描述了星形胶质细胞肿胀和细胞毒性水肿在BM治疗期间放射性脑水肿进展中的新作用。虽然放射性水肿一直被完全归因于血脑屏障(BBB)的破坏及随之而来的血管源性效应,但我们的结果表明,在急性情况下影响星形胶质细胞的细胞毒性水肿在BM标准治疗期间脑水肿的进展中起重要作用。目前脑水肿的标准治疗包括用类固醇进行预处理,仅在出现临床显著水肿后使用贝伐单抗。这两种干预措施都被认为是针对血管源性水肿的。本研究表明,BM患者使用已获美国食品药品监督管理局(FDA)批准的抗癫痫药物对放射性诱导的细胞毒性水肿进行急性和临时预防性治疗可能会有额外益处。这种早期预防策略可以很容易地在临床上实施,目标是将治疗相关毒性降至最低。

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