Department of Chemistry and COSDAF (Centre of Super-Diamond and Advanced Films), City University of Hong Kong, 83 Tat Chee Avenue, Kowloon, Hong Kong 999077, China.
Shenzhen Research Institute of City University of Hong Kong, Shenzhen 518057, China.
Anal Chem. 2024 Feb 13;96(6):2406-2414. doi: 10.1021/acs.analchem.3c04319. Epub 2024 Feb 3.
Glioblastoma multiforme (GBM) is a highly aggressive primary brain tumor associated with limited treatment options and high drug resistance, presenting significant challenges in the pursuit of effective treatment strategies. Epigenetic modifications have emerged as promising diagnostic biomarkers and therapeutic targets for GBM. For instance, histone deacetylase 6 (HDAC6) has been identified as a potential pharmacological target for GBM. Furthermore, the overexpression of monoamine oxidase A (MAO A) in glioma has been linked to tumor progression, making it an attractive target for therapy. In this study, we successfully engineered , an activatable multifunctional small-molecule probe with the goal of efficiently detecting and killing glioma cells. can be selectively activated by HDAC6, leading to the "turn on" of near-infrared fluorescence and effective inhibition of MAO A, along with potent photodynamic therapy (PDT) effects. Consequently, not only enables the imaging of HDAC6 in live glioma cells but also exhibits the synergistic effect of MAO A inhibition and PDT, effectively inhibiting glioma invasion and inducing cellular apoptosis. The distinctive combination of features displayed by positions it as a versatile and highly effective tool for the accurate diagnosis and treatment of glioma cells. This opens up opportunities to enhance therapy outcomes and explore future applications in glioma theranostics.
多形性胶质母细胞瘤(GBM)是一种高度侵袭性的原发性脑肿瘤,治疗选择有限,耐药性高,这给寻找有效的治疗策略带来了重大挑战。表观遗传修饰已成为 GBM 的有前途的诊断生物标志物和治疗靶点。例如,组蛋白去乙酰化酶 6(HDAC6)已被确定为 GBM 的潜在药物靶点。此外,单胺氧化酶 A(MAO A)在神经胶质瘤中的过表达与肿瘤进展有关,使其成为治疗的有吸引力的靶点。在这项研究中,我们成功地设计了一种可激活的多功能小分子探针,旨在有效地检测和杀死神经胶质瘤细胞。可以被 HDAC6 选择性激活,导致近红外荧光的“开启”和 MAO A 的有效抑制,以及有效的光动力治疗(PDT)效应。因此,不仅可以在活的神经胶质瘤细胞中成像 HDAC6,还可以显示 MAO A 抑制和 PDT 的协同作用,有效抑制神经胶质瘤的侵袭并诱导细胞凋亡。的独特特征组合使其成为一种多功能且高效的工具,可用于准确诊断和治疗神经胶质瘤细胞。这为提高治疗效果和探索神经胶质瘤治疗学的未来应用提供了机会。