Shared mechanisms among neurodegenerative diseases: from genetic factors to gene networks

被引:38
|
作者
Arneson, Douglas [1 ]
Zhang, Yong [1 ,2 ]
Yang, Xia [1 ]
Narayanan, Manikandan [3 ,4 ,5 ]
机构
[1] Univ Calif Los Angeles, Dept Integrat Biol & Physiol, Los Angeles, CA 90095 USA
[2] Shandong Univ, Shandong Prov Qianfoshan Hosp, Dept Cardiol, Jinan 250014, Shandong, Peoples R China
[3] NIAID, Syst Genom & Bioinformat Unit, Lab Syst Biol, NIH, 9000 Rockville Pike, Bethesda, MD 20892 USA
[4] Indian Inst Technol IIT Madras, Dept Comp Sci & Engn CSE, Madras 600036, Tamil Nadu, India
[5] Indian Inst Technol IIT Madras, Initiat Biol Syst Engn IBSE, Robert Bosch Ctr Data Sci & Artificial Intelligen, Madras 600036, Tamil Nadu, India
基金
美国国家卫生研究院;
关键词
Alzheimer's disease; Parkinson's disease; amyotrophic lateral sclerosis; neurodegenerative diseases; shared molecular signatures; genomics; AMYOTROPHIC-LATERAL-SCLEROSIS; HERITABILITY; ALZHEIMERS; BIOLOGY; RISK; AGE;
D O I
10.1007/s12041-018-0963-3
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Neurodegenerative diseases such as Alzheimer's disease, Parkinson's disease, and amyotrophic lateral sclerosis are pressing health concerns in modern societies for which effective therapies are still lacking. Recent high-throughput genomic technologies have enabled genome-scale, multidimensional investigations to facilitate a better understanding of the underlying mechanisms and the identification of novel targets. Here we review the molecular insights gained through such studies, and compare the similarities and differences between neurodegenerative diseases revealed by systems genomics and gene network modelling approaches. We focus specifically on the shared mechanisms at multiple molecular scales ranging from genetic factors to gene expression to network-level features of gene regulation, and whenever possible also point out mechanisms that distinguish one disease from another. Our review sets the stage for similar genomewide inspection in the future on shared/distinct features of neurodegenerative diseases at the levels of cellular, proteomic or epigenomic signatures, and how these features may interact to determine the progression and treatment response of different diseases afflicting the same individual.
引用
收藏
页码:795 / 806
页数:12
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