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碳酸酐酶抑制剂E7070使胶质母细胞瘤细胞对放疗和化疗敏感并减少肿瘤生长。

The Carbonic Anhydrase Inhibitor E7070 Sensitizes Glioblastoma Cells to Radio- and Chemotherapy and Reduces Tumor Growth.

作者信息

Teixeira Silvia A, Viapiano Mariano S, Andrade Augusto F, Nandhu Mohan S, Pezuk Julia A, Bidinotto Lucas T, Suazo Veridiana K, Neder Luciano, Carlotti Carlos G, Becker Aline P, Tone Luiz Gonzaga, Scrideli Carlos A

机构信息

Department of Paediatrics, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.

Department of Neurosurgery, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.

出版信息

Mol Neurobiol. 2021 Sep;58(9):4520-4534. doi: 10.1007/s12035-021-02437-3. Epub 2021 Jun 3.

DOI:10.1007/s12035-021-02437-3
PMID:34085182
Abstract

Glioblastomas (GBMs), the most common and lethal primary brain tumor, show inherent infiltrative nature and high molecular heterogeneity that make complete surgical resection unfeasible and unresponsive to conventional adjuvant therapy. Due to their fast growth rate even under hypoxic and acidic conditions, GBM cells can conserve the intracellular pH at physiological range by overexpressing membrane-bound carbonic anhydrases (CAs). The synthetic sulfonamide E7070 is a potent inhibitor of CAs that harbors putative anticancer properties; however, this drug has still not been tested in GBMs. The present study aimed to evaluate the effects of E7070 on CA9 and CA12 enzymes in GBM cells as well as in the tumor cell growth, migration, invasion, and resistance to radiotherapy and chemotherapy. We found that E7070 treatment significantly reduced tumor cell growth and increased radio- and chemotherapy efficacy against GBM cells under hypoxia. Our data suggests that E7070 has therapeutic potential as a radio-chemo-sensitizing in drug-resistant GBMs, representing an attractive strategy to improve the adjuvant therapy. We showed that CA9 and CA12 represent potentially valuable therapeutic targets that should be further investigated as useful diagnostic and prognostic biomarkers for GBM tailored therapy.

摘要

胶质母细胞瘤(GBM)是最常见且致命的原发性脑肿瘤,具有内在的浸润性和高度的分子异质性,这使得完整的手术切除不可行,且对传统辅助治疗无反应。由于其即使在缺氧和酸性条件下仍具有快速生长的特性,GBM细胞可通过过度表达膜结合碳酸酐酶(CA)将细胞内pH维持在生理范围内。合成磺酰胺E7070是一种具有潜在抗癌特性的CA强效抑制剂;然而,该药物尚未在GBM中进行测试。本研究旨在评估E7070对GBM细胞中CA9和CA12酶的影响,以及对肿瘤细胞生长、迁移、侵袭以及放疗和化疗耐药性的影响。我们发现,E7070处理可显著降低肿瘤细胞生长,并增强缺氧条件下GBM细胞对放疗和化疗的疗效。我们的数据表明,E7070作为耐药GBM的放疗化疗增敏剂具有治疗潜力,是改善辅助治疗的一种有吸引力的策略。我们表明,CA9和CA12是潜在有价值的治疗靶点,作为GBM定制治疗有用的诊断和预后生物标志物应进一步研究。

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本文引用的文献

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Mechanisms of temozolomide resistance in glioblastoma - a comprehensive review.胶质母细胞瘤中替莫唑胺耐药的机制——综述
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Proton Transport in Cancer Cells: The Role of Carbonic Anhydrases.质子在癌细胞中的转运:碳酸酐酶的作用。
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Targeting hypoxia in the tumor microenvironment: a potential strategy to improve cancer immunotherapy.针对肿瘤微环境中的缺氧:提高癌症免疫疗法的潜在策略。
PI3K/AKT/mTOR pathway, hypoxia, and glucose metabolism: Potential targets to overcome radioresistance in small cell lung cancer.
PI3K/AKT/mTOR信号通路、缺氧与葡萄糖代谢:克服小细胞肺癌放射抗性的潜在靶点
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Indisulam Reduces Viability and Regulates Apoptotic Gene Expression in Pediatric High-Grade Glioma Cells.茚地那韦降低小儿高级别胶质瘤细胞的活力并调节凋亡基因表达。
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