Detecting early-warning signals of type 1 diabetes and its leading biomolecular networks by dynamical network biomarkers

被引:71
作者
Liu, Xiaoping [1 ]
Liu, Rui [2 ,3 ]
Zhao, Xing-Ming [4 ]
Chen, Luonan [1 ,3 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Biol Sci, SIBS Novo Nordisk Translat Res Ctr PreDiabet, Key Lab Syst Biol, Shanghai 200031, Peoples R China
[2] S China Univ Technol, Dept Math, Guangzhou 510640, Guangdong, Peoples R China
[3] Univ Tokyo, Inst Ind Sci, Collaborat Res Ctr Innovat Math Modelling, Tokyo 1538505, Japan
[4] Tongji Univ, Sch Elect & Informat Engn, Dept Comp Sci, Shanghai, Peoples R China
基金
中国国家自然科学基金; 日本学术振兴会;
关键词
DISEASE GENES; NOD MOUSE; MODEL; CELLS; IDENTIFICATION; PROGRESSION; APOPTOSIS;
D O I
10.1186/1755-8794-6-S2-S8
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background: Type 1 diabetes (T1D) is a complex disease and harmful to human health, and most of the existing biomarkers are mainly to measure the disease phenotype after the disease onset (or drastic deterioration). Until now, there is no effective biomarker which can predict the upcoming disease (or pre-disease state) before disease onset or disease deterioration. Further, the detail molecular mechanism for such deterioration of the disease, e. g., driver genes or causal network of the disease, is still unclear. Methods: In this study, we detected early-warning signals of T1D and its leading biomolecular networks based on serial gene expression profiles of NOD (non-obese diabetic) mice by identifying a new type of biomarker, i.e., dynamical network biomarker (DNB) which forms a specific module for marking the time period just before the drastic deterioration of T1D. Results: Two dynamical network biomarkers were obtained to signal the emergence of two critical deteriorations for the disease, and could be used to predict the upcoming sudden changes during the disease progression. We found that the two critical transitions led to peri-insulitis and hyperglycemia in NOD mices, which are consistent with other independent experimental results from literature. Conclusions: The identified dynamical network biomarkers can be used to detect the early-warning signals of T1D and predict upcoming disease onset before the drastic deterioration. In addition, we also demonstrated that the leading biomolecular networks are causally related to the initiation and progression of T1D, and provided the biological insight into the molecular mechanism of T1D. Experimental data from literature and functional analysis on DNBs validated the computational results.
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页数:10
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共 24 条
[1]   The NOD mouse: A model of immune dysregulation [J].
Anderson, MS ;
Bluestone, JA .
ANNUAL REVIEW OF IMMUNOLOGY, 2005, 23 :447-485
[2]   The NOD mouse model of type 1 diabetes: As good as it gets? [J].
Atkinson, MA ;
Leiter, EH .
NATURE MEDICINE, 1999, 5 (06) :601-604
[3]   Detecting early-warning signals for sudden deterioration of complex diseases by dynamical network biomarkers [J].
Chen, Luonan ;
Liu, Rui ;
Liu, Zhi-Ping ;
Li, Meiyi ;
Aihara, Kazuyuki .
SCIENTIFIC REPORTS, 2012, 2
[4]   An integrated transcriptomic and computational analysis for biomarker identification in gastric cancer [J].
Cui, Juan ;
Chen, Yunbo ;
Chou, Wen-Chi ;
Sun, Liankun ;
Chen, Li ;
Suo, Jian ;
Ni, Zhaohui ;
Zhang, Ming ;
Kong, Xiaoxia ;
Hoffman, Lisabeth L. ;
Kang, Jinsong ;
Su, Yingying ;
Olman, Victor ;
Johnson, Darryl ;
Tench, Daniel W. ;
Amster, I. Jonathan ;
Orlando, Ron ;
Puett, David ;
Li, Fan ;
Xu, Ying .
NUCLEIC ACIDS RESEARCH, 2011, 39 (04) :1197-1207
[5]   Oxidative Stress and Redox Modulation Potential in Type 1 Diabetes [J].
Delmastro, Meghan M. ;
Piganelli, Jon D. .
CLINICAL & DEVELOPMENTAL IMMUNOLOGY, 2011,
[6]   The nonobese diabetic mouse as a model of autoimmune diabetes: Immune dysregulation gets the NOD [J].
Delovitch, TL ;
Singh, B .
IMMUNITY, 1997, 7 (06) :727-738
[7]   Type 1 diabetes: virus infection or autoimmune disease? [J].
Fairweather, D ;
Rose, NR .
NATURE IMMUNOLOGY, 2002, 3 (04) :338-340
[8]   Pancreatic lymph nodes are required for priming of β cell reactive T cells in NOD mice [J].
Gagnerault, MC ;
Luan, JJ ;
Lotton, C ;
Lepault, F .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 196 (03) :369-377
[9]   Pancreatic lymph node-derived CD4+CD25+ Treg cells:: Highly potent regulators of diabetes that require TRANCE-RANK signals [J].
Green, EA ;
Choi, YW ;
Flavell, RA .
IMMUNITY, 2002, 16 (02) :183-191
[10]   Coexpression network analysis in chronic hepatitis B and C hepatic lesions reveals distinct patterns of disease progression to hepatocellular carcinoma [J].
He, Danning ;
Liu, Zhi-Ping ;
Honda, Masao ;
Kaneko, Shuichi ;
Chen, Luonan .
JOURNAL OF MOLECULAR CELL BIOLOGY, 2012, 4 (03) :140-152