摘要
不受胆碱能神经元支配的上皮细胞表达烟碱型和毒蕈碱型乙酰胆碱能(ACh)受体(nAChR,MAChR)。nAChR和MAChR是非神经元ACh释放的自动/伴分泌-调节循环的组成部分。非神经元细胞的胆碱能控制可能是由这些受体引起的不同作用(协同、增加、或相互)所介导的。离子活动(Ca+2注入)是通过nAChR通路的ACh开放而形成,而代谢活动是通过ACh-结合至G-蛋白偶联的mAChR而形成。有效的细胞间和细胞内信号传导对于癌细胞的增殖和存活是至关重要的。根据肿瘤细胞类型,不同的AChR被确定。气道上皮细胞和胰腺癌细胞的扩散分别是通过α7-nAChR和M3-mAChR控制的,而乳腺癌细胞和结肠癌细胞分别是通过 α9-nAChR和 M3-mAChR控制的。反之,这些受体可能激活不同通路(Ras-Raf-1-Erk-AKT)和其他受体(β- 肾上腺素能受体)。nAChR 或 mAChR 拮抗剂或许可以抑制肿瘤生长。通过反义或拮抗剂(达非那新,噻托溴铵)抑制M3是肺癌或结肠癌扩散减少,α9- nAChR [多酚(-)-表没食子儿茶素-3-没食子酸盐]的抑制是乳腺癌细胞的生长减少。 α7-nAChR沉默抑制肺癌扩散。另外,nAChR-β-肾上腺素能受体通路的抑制(β-阻断剂)也可能有效。本文将描述关于许多在治疗中具有挑战的复杂疾病,如癌症,中胆碱能受体药物抑制的未来将发挥的作用。癌症发生是在疾病恶化过程中改变了相关器官细胞中受疾病扰乱的分子网络的结果。通过系统的方法才能解决这些挑战。
关键词: ACh,复杂疾病,药物发现和发展,mAChR
Current Molecular Medicine
Title:Cholinergic Receptors as Target for Cancer Therapy in a Systems Medicine Perspective
Volume: 14 Issue: 9
Author(s): P. Russo, A. Del Bufalo, G. Salinaro, M. Fini and A. Cesario
Affiliation:
关键词: ACh,复杂疾病,药物发现和发展,mAChR
摘要: Epithelial cells not innervated by cholinergic neurons express nicotinic and muscarinic acetylcholine (ACh) receptors (nAChR, mAChR). nAChR and mAChR are components of the auto-/paracrine-regulatory loop of non-neuronal ACh release. The cholinergic control of non-neuronal cells may be mediated by different effects (synergistic, additive, or reciprocal) triggered by these receptors. The ionic events (Ca+2 influx) are generated by the ACh-opening of nAChR channels, while the metabolic events by ACh-binding to G-proteincoupled mAChR. Effective inter- and intracellular signaling is crucial for valuable cancer cells proliferation and survival. Depending on cancer cell type, different AChR have been identified. The proliferation of airways epithelial cancer cells and pancreatic cancer cells may be under the control of α7-nAChR and M3-mAChR, while breast cancer cells and colon cancer cells are regulated by α9-nAChR, and M3-mAChR, respectively. In turn, these receptors may activate different pathways (Ras-Raf-1-Erk-AKT) as well as other receptors (β- adrenergicR). nAChR or mAChR antagonists may inhibit cancer growth. Inhibition of M3 by antisense or antagonists (Darifenacin, Tiotropium) reduces lung or colon cancer proliferation, as well as inhibition of α9- nAChR [polyphenol (-)-epigallocatechin-3-gallate] diminishes breast cancer cells growth. α7-nAChR silencing inhibits lung cancer proliferation. Moreover, inhibition of the nAChR-β-adrenergicR pathway (β-blockers) could be also useful. This review will describe the future translational perspectives of cholinergic receptors druginhibition in a complex disease such as cancer that poses compelling treatment challenges. Cancer happens as consequence of disease-perturbed molecular networks in relevant organ cells that change during progression. The framework for approaching these challenges is a systems approach.
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Russo P., Bufalo Del A., Salinaro G., Fini M. and Cesario A., Cholinergic Receptors as Target for Cancer Therapy in a Systems Medicine Perspective, Current Molecular Medicine 2014; 14 (9) . https://dx.doi.org/10.2174/1566524014666141015152601
DOI https://dx.doi.org/10.2174/1566524014666141015152601 |
Print ISSN 1566-5240 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5666 |
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