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靶向胶质母细胞瘤干细胞:用于胶质母细胞瘤可视化和治疗的A40s适配体-近红外染料偶联物

Targeting Glioblastoma Stem Cells: A40s Aptamer-NIR-Dye Conjugate for Glioblastoma Visualization and Treatment.

作者信息

Affinito Alessandra, Ingenito Francesco, Verde Sara, Musella Emanuele, Pattanayak Birlipta, Fiore Danilo, Quintavalle Cristina, Fraticelli Aurelia, Mascolo Martina, Petrillo Gianluca, Pignataro Claudia, De Luca Giada, Mezzanotte Laura, Condorelli Gerolama

机构信息

Department of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, 80131 Naples, Italy.

AKA Biotech, 80131 Naples, Italy.

出版信息

Biomolecules. 2025 May 27;15(6):768. doi: 10.3390/biom15060768.

Abstract

Glioblastoma (GBM) is the most aggressive and challenging brain cancer, in terms of diagnosis and therapy. The highly infiltrative glioblastoma stem cells (GSCs) are difficult to visualize and surgically remove with the current diagnostic tools, which often lead to misdiagnosis and false-positive results. In this study, we focused on a groundbreaking tool for specifically visualizing and removing GSCs. We exploited the specific binding of A40s aptamer to EphA2 for the selective delivery of Near-Infrared Dyes (NIR-Dyes), like IR700DX and ICG, both in vitro and in vivo. The A40s aptamer, engineered through the NIR-Dye conjugation, did not affect aptamer binding ability; indeed, A40s-NIR-Dye conjugates bound GLI261 stem-like cells and patient-derived GSCs in vitro; moreover, they induced cell death upon photodynamic therapy treatment (PDT). Additionally, when systemically administrated, the A40s-NIR-Dye conjugates allowed GSC visualization and accumulated in tumor mass. This allows GSCs detection and treatment. Our findings demonstrate the potential use of A40s aptamer as a targeted therapeutic approach and imaging tool in vivo for GSCs, paving the way for improved, more effective, and less invasive GBM management.

摘要

胶质母细胞瘤(GBM)是诊断和治疗方面最具侵袭性且极具挑战性的脑癌。高度浸润性的胶质母细胞瘤干细胞(GSCs)难以通过当前的诊断工具进行可视化和手术切除,这常常导致误诊和假阳性结果。在本研究中,我们聚焦于一种用于特异性可视化和清除GSCs的开创性工具。我们利用A40s适配体与EphA2的特异性结合,在体外和体内选择性递送近红外染料(NIR-Dyes),如IR700DX和ICG。通过与NIR-Dye偶联改造的A40s适配体,并未影响适配体的结合能力;实际上,A40s-NIR-Dye偶联物在体外可结合GLI261干细胞样细胞和患者来源的GSCs;此外,它们在光动力疗法(PDT)治疗后可诱导细胞死亡。另外,当进行全身给药时,A40s-NIR-Dye偶联物可实现GSCs可视化并在肿瘤块中蓄积。这使得能够检测和治疗GSCs。我们的研究结果证明了A40s适配体作为体内针对GSCs的靶向治疗方法和成像工具的潜在用途,为改进、更有效且侵入性更小的GBM管理铺平了道路。

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