Discover the network mechanisms underlying the connections between aging and age-related diseases

被引:40
作者
Yang, Jialiang [1 ,2 ]
Huang, Tao [1 ,2 ,5 ]
Song, Won-min [1 ,2 ]
Petralia, Francesca [1 ,2 ]
Mobbs, Charles V. [3 ,4 ]
Zhang, Bin [1 ,2 ]
Zhao, Yong [1 ,2 ]
Schadt, Eric E. [1 ,2 ]
Zhu, Jun [1 ,2 ]
Tu, Zhidong [1 ,2 ]
机构
[1] Icahn Sch Med Mt Sinai, Inst Genom & Multiscale Biol, New York, NY 10029 USA
[2] Icahn Sch Med Mt Sinai, Dept Genet & Genom Sci, New York, NY 10029 USA
[3] Icahn Sch Med Mt Sinai, Dept Neurosci, New York, NY 10029 USA
[4] Icahn Sch Med Mt Sinai, Dept Geriatr & Palliat Med, New York, NY 10029 USA
[5] Chinese Acad Sci, Shanghai Inst Biol Sci, Inst Hlth Sci, Shanghai 200031, Peoples R China
关键词
ELECTRON-TRANSPORT CHAIN; ALZHEIMERS-DISEASE; INFLAMMATION; PREVALENCE; DEFICIENCY; MUTATIONS; LONGEVITY; DEMENTIA; BIOLOGY; CANCER;
D O I
10.1038/srep32566
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Although our knowledge of aging has greatly expanded in the past decades, it remains elusive why and how aging contributes to the development of age-related diseases (ARDs). In particular, a global mechanistic understanding of the connections between aging and ARDs is yet to be established. We rely on a network modelling named "GeroNet" to study the connections between aging and more than a hundred diseases. By evaluating topological connections between aging genes and disease genes in over three thousand subnetworks corresponding to various biological processes, we show that aging has stronger connections with ARD genes compared to non-ARD genes in subnetworks corresponding to "response to decreased oxygen levels", "insulin signalling pathway", "cell cycle", etc. Based on subnetwork connectivity, we can correctly "predict" if a disease is age-related and prioritize the biological processes that are involved in connecting to multiple ARDs. Using Alzheimer's disease (AD) as an example, GeroNet identifies meaningful genes that may play key roles in connecting aging and ARDs. The top modules identified by GeroNet in AD significantly overlap with modules identified from a large scale AD brain gene expression experiment, supporting that GeroNet indeed reveals the underlying biological processes involved in the disease.
引用
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页数:12
相关论文
共 61 条
[1]   Gene Ontology: tool for the unification of biology [J].
Ashburner, M ;
Ball, CA ;
Blake, JA ;
Botstein, D ;
Butler, H ;
Cherry, JM ;
Davis, AP ;
Dolinski, K ;
Dwight, SS ;
Eppig, JT ;
Harris, MA ;
Hill, DP ;
Issel-Tarver, L ;
Kasarskis, A ;
Lewis, S ;
Matese, JC ;
Richardson, JE ;
Ringwald, M ;
Rubin, GM ;
Sherlock, G .
NATURE GENETICS, 2000, 25 (01) :25-29
[2]   Insulin-like growth factor 1 (IGF-1) and aging: controversies and new insights [J].
Bartke, A ;
Chandrashekar, V ;
Dominici, F ;
Turyn, D ;
Kinney, B ;
Steger, R ;
Kopchick, JJ .
BIOGERONTOLOGY, 2003, 4 (01) :1-8
[3]   Inflammation: a culprit for vascular calcification in atherosclerosis and diabetes [J].
Bessueille, L. ;
Magne, D. .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2015, 72 (13) :2475-2489
[4]   Answering the ultimate question "What is the Proximal Cause of Aging?" [J].
Blagosklonny, Mikhail V. .
AGING-US, 2012, 4 (12) :861-877
[5]  
Bondy S, 2010, OXID STRESS APPL BAS, P339, DOI 10.1007/978-1-60761-602-3_17
[6]   THE TRIGLYCERIDE ISSUE - A VIEW FROM FRAMINGHAM [J].
CASTELLI, WP .
AMERICAN HEART JOURNAL, 1986, 112 (02) :432-437
[7]  
Dai Dao-Fu, 2014, Longev Healthspan, V3, P6, DOI 10.1186/2046-2395-3-6
[8]   How ageing processes influence cancer [J].
de Magalhaes, Joao Pedro .
NATURE REVIEWS CANCER, 2013, 13 (05) :357-365
[9]   Dipeptidyl peptidase-4 inhibitors in the treatment of type 2 diabetes: a comparative review [J].
Deacon, C. F. .
DIABETES OBESITY & METABOLISM, 2011, 13 (01) :7-18
[10]   Correlates of p53- and Fas (CD95)-mediated apoptosis in Alzheimer's disease [J].
delaMonte, SM ;
Sohn, YK ;
Wands, JR .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1997, 152 (01) :73-83