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首页> 外文期刊>Current drug metabolism >Translational Shift of HSP90 as a Novel Therapeutic Target from Cancer to Neurodegenerative Disorders: An Emerging Trend in the Cure of Alzheimer's and Parkinson's Diseases
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Translational Shift of HSP90 as a Novel Therapeutic Target from Cancer to Neurodegenerative Disorders: An Emerging Trend in the Cure of Alzheimer's and Parkinson's Diseases

机译:HSP90的翻译转移作为从癌症到神经退行性疾病的新疗法靶标:Alzheimer和帕金森病治愈的新兴趋势

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摘要

Background: Despite having extensive research, the apparent pathogenic mechanism of Alzheimer's disease (AD), Parkinson's disease (PD) and other neurodegenerative diseases (NDs) have not yet fully understood. The Heat Shock Protein 90 (HSP90), a ubiquitous molecular chaperone, found to have an important role in averting protein misfolding and aggregation through inhibition of apoptotic activity in neuro-inflammatory diseases. Various researchers have confirmed its role in maintaining aberrant neuronal protein's functional stability to a great capacity. It is also involved in regulating the activity of the heat shock factor-1 (HSF-1), a vital regulator of the heat shock response mechanism that cells employ to protect themselves against stress conditions. This quality makes the HSP90 an ideal candidate for novel inhibitory target for therapeutic modality in NDs.
机译:背景:尽管具有广泛的研究,Alzheimer疾病(AD),帕金森病(Pd)和其他神经退行性疾病(NDS)的表观致病机制尚未完全理解。 热休克蛋白90(HSP90),一种普遍的分子伴侣,发现通过抑制神经炎症疾病的凋亡活性来具有重要作用。 各种研究人员已经证实了其在维持异常神经元蛋白的功能稳定性方面的作用。 它还涉及调节热休克因子-1(HSF-1)的活性,该热休克响应机构的重要调节器,该细胞用于保护自己免受应力条件。 该质量使HSP90成为NDS中治疗方式的新型抑制靶标的理想候选者。

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