School of Pharmacy, College of Pharmacy, Taipei Medical University, 250 Wuxing Street, Taipei 11031, Taiwan.
Department of Biotechnology, Jaypee Institute of Information Technology, Noida 201307, India.
J Med Chem. 2022 Jul 14;65(13):8596-8685. doi: 10.1021/acs.jmedchem.1c01946. Epub 2022 Jul 5.
Glioblastoma (GBM) is a highly malignant brain tumor characterized by a heterogeneous population of genetically unstable and highly infiltrative cells that are resistant to chemotherapy. Although substantial efforts have been invested in the field of anti-GBM drug discovery in the past decade, success has primarily been confined to the preclinical level, and clinical studies have often been hampered due to efficacy-, selectivity-, or physicochemical property-related issues. Thus, expansion of the list of molecular targets coupled with a pragmatic design of new small-molecule inhibitors with central nervous system (CNS)-penetrating ability is required to steer the wheels of anti-GBM drug discovery endeavors. This Perspective presents various aspects of drug discovery (challenges in GBM drug discovery and delivery, therapeutic targets, and agents under clinical investigation). The comprehensively covered sections include the recent medicinal chemistry campaigns embarked upon to validate the potential of numerous enzymes/proteins/receptors as therapeutic targets in GBM.
胶质母细胞瘤(GBM)是一种高度恶性的脑肿瘤,其特征是存在遗传不稳定和高度浸润性的异质性细胞群体,对化疗具有耐药性。尽管在过去十年中,人们在抗 GBM 药物发现领域投入了大量的努力,但主要的成功仅限于临床前水平,而且由于疗效、选择性或理化性质相关的问题,临床研究往往受到阻碍。因此,需要扩大分子靶标的列表,并设计具有中枢神经系统(CNS)穿透能力的新型小分子抑制剂,以推动抗 GBM 药物发现的努力。本观点介绍了药物发现的各个方面(GBM 药物发现和传递的挑战、治疗靶点和临床研究中的药物)。全面涵盖的部分包括最近开展的药物化学研究,以验证许多酶/蛋白质/受体作为 GBM 治疗靶点的潜力。