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Therapeutic potential of RNA interference for neurological disorders

机译:RNA干扰对神经系统疾病的治疗潜力

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摘要

During the past decade, numerous molecular mediators of neurodegenerative diseases and neurological disorders have been identified and validated, yet few novel therapies have emerged and the unmet medical needs remain high. These molecular mediators belong to target classes such as ion channels, neurotransmitters and neurotransmitter receptors, cytokines, growth factors, enzymes and other proteins. In some cases, substantial pre-clinical validation exists, but the molecular target has not been readily druggable with small molecules, proteins or antibodies. RNA interference represents a therapeutic approach applicable to such non-druggable targets. Both non-viral and viral delivery strategies are being undertaken for in vivo silencing of molecular targets by RNA interference, which has resulted in robust efficacy in animal models of Alzheimer's disease, ALS, Huntington's disease, spinocerebellar ataxia, anxiety, depression, neuropathic pain, encephalitis and glioblastoma. These proof-of-concept data in animal models, together with the commencement of clinical trials using RNA interference for macular degeneration and respiratory syncytial virus infection, point to the potential of direct RNA interference for neurological disorders and neurodegenerative diseases. (c) 2006 Elsevier Inc. All rights reserved.
机译:在过去的十年中,已经鉴定并验证了神经退行性疾病和神经系统疾病的多种分子介体,但很少出现新的疗法,未满足的医疗需求仍然很高。这些分子介质属于靶类别,例如离子通道,神经递质和神经递质受体,细胞因子,生长因子,酶和其他蛋白质。在某些情况下,存在大量的临床前验证,但分子靶标尚不易与小分子,蛋白质或抗体一起制成药物。 RNA干扰代表了适用于此类非药物靶标的治疗方法。正在通过RNA干扰在体内沉默分子靶标的非病毒和病毒递送策略,已在阿尔茨海默氏病,ALS,亨廷顿氏病,脊髓小脑共济失调,焦虑,抑郁,神经性疼痛,脑炎和胶质母细胞瘤。动物模型中的这些概念验证数据,以及使用RNA干扰治疗黄斑变性和呼吸道合胞病毒感染的临床试验的开展,都表明直接RNA干扰在神经系统疾病和神经退行性疾病中的潜力。 (c)2006 Elsevier Inc.保留所有权利。

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