Lazarevic-Pasti Tamara, Leskovac Andreja, Momic Tatjana, Petrovic Sandra, Vasic Vesna
Department of Physical Chemistry, Vinca Institute of Nuclear Sciences, University of Belgrade, M. Petrovica Alasa 12-14, 11001 Belgrade. Serbia.
Curr Med Chem. 2017;24(30):3283-3309. doi: 10.2174/0929867324666170705123509.
Acetylcholinesterase (AChE) is involved in the termination of impulse transmission by rapid hydrolysis of the neurotransmitter acetylcholine in numerous cholinergic pathways in the central and peripheral nervous systems. The enzyme inactivation leads to acetylcholine accumulation, hyperstimulation of nicotinic and muscarinic receptors, and disrupted neurotransmission. Hence, acetylcholinesterase inhibitors, interacting with the enzyme as their primary target, are applied as relevant drugs for different neurodegenerative diseases (such as Alzheimer's and Parkinson's) as well as toxins. At the same time, there are increasing evidence that in non-neuronal context, AChE is involved in the regulation of cell proliferation, differentiation, apoptosis and cell-cell interaction. An irregular expression of AChE has been found in different types of tumors, suggesting the involvement of AChE in the regulation of tumor development. Having all this in mind, there is a possibility that some AChE inhibitors could be used as anti-cancer agents.
This contribution will discuss a broad range of possible application of different AChE inhibitors as drugs, from well-known anti-Alzheimer's disease drugs to their use in cancer treatment in future. Emphasis will be put on various known AChE inhibitors classes, whose application as drugs could be controversy, as well as on newly investigated natural products, which can also modulate AChE activity.
It is not clear a patient treated for neurodegenerative condition prone to increased risk for some types of cancer and vice versa. This is necessary to keep in mind during rational drug design process for all therapies, which are based on AChE as a target molecule.
乙酰胆碱酯酶(AChE)通过在中枢和外周神经系统的众多胆碱能途径中快速水解神经递质乙酰胆碱,参与冲动传递的终止。该酶失活会导致乙酰胆碱积累、烟碱样和毒蕈碱样受体过度刺激以及神经传递中断。因此,作为主要作用靶点与该酶相互作用的乙酰胆碱酯酶抑制剂,被用作治疗不同神经退行性疾病(如阿尔茨海默病和帕金森病)的相关药物以及毒素。同时,越来越多的证据表明,在非神经元环境中,AChE参与细胞增殖、分化、凋亡及细胞间相互作用的调节。在不同类型的肿瘤中已发现AChE表达异常,这表明AChE参与肿瘤发展的调控。考虑到所有这些因素,一些AChE抑制剂有可能被用作抗癌药物。
本论文将讨论不同AChE抑制剂作为药物的广泛可能应用,从著名的抗阿尔茨海默病药物到其未来在癌症治疗中的应用。重点将放在各种已知的AChE抑制剂类别上,其作为药物的应用可能存在争议,以及新研究的天然产物上,它们也能调节AChE活性。
尚不清楚接受神经退行性疾病治疗的患者是否更容易患某些类型的癌症,反之亦然。在以AChE为靶分子的所有治疗的合理药物设计过程中,必须牢记这一点。