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基因组学和蛋白质组学在理解帕金森病中修饰因子作用方面的贡献。

Contribution of genomics and proteomics in understanding the role of modifying factors in Parkinson's disease.

作者信息

Singh M P, Patel S, Dikshit M, Gupta Y K

机构信息

Industrial Toxicology Research Centre, Lucknow 226 001, UP, India.

出版信息

Indian J Biochem Biophys. 2006 Apr;43(2):69-81.

Abstract

Parkinson's disease (PD) is a complex neurological disorder, characterized by selective degeneration of nigrostriatal dopaminergic neurons. It is a multi-factorial disease, contributed by a combination of age, genetic and environmental factors. Etiology of sporadic PD and mechanism underlying selective loss of dopaminergic neurons has not yet been clearly understood. Recent developments in genomics and proteomics have revolutionized the research on PD at genetic level. Differential gene expression patterns (DNA biochip technology), age-dependent complex genetic patterns (SNP genotyping), and protein expression profiles (proteomics) of PD patients have started providing the specific and rigorous molecular explanation and role of modifying factors in PD. Genomics and proteomics are further expected to help in developing biomarkers for diagnosis of early onset PD and also to develop valuable and potential therapeutic strategies for its treatment. In this review, we have discussed the progress made by genomics and proteomics, in understanding the role of modifying factors in PD.

摘要

帕金森病(PD)是一种复杂的神经疾病,其特征为黑质纹状体多巴胺能神经元的选择性退化。它是一种多因素疾病,由年龄、遗传和环境因素共同作用所致。散发性帕金森病的病因以及多巴胺能神经元选择性丧失的潜在机制尚未完全明确。基因组学和蛋白质组学的最新进展在基因层面彻底改变了帕金森病的研究。帕金森病患者的差异基因表达模式(DNA生物芯片技术)、年龄依赖性复杂遗传模式(单核苷酸多态性基因分型)以及蛋白质表达谱(蛋白质组学)已开始为帕金森病中修饰因子的具体和严格分子解释及作用提供依据。基因组学和蛋白质组学有望进一步帮助开发早期帕金森病诊断的生物标志物,并为其治疗制定有价值的潜在治疗策略。在本综述中,我们讨论了基因组学和蛋白质组学在理解修饰因子在帕金森病中的作用方面所取得的进展。

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