Quantifying critical states of complex diseases using single-sample dynamic network biomarkers

被引:84
作者
Liu, Xiaoping [1 ,2 ,3 ,4 ]
Chang, Xiao [1 ,2 ]
Liu, Rui [5 ]
Yu, Xiangtian [3 ]
Chen, Luonan [1 ,3 ,6 ]
Aihara, Kazuyuki [1 ]
机构
[1] Univ Tokyo, Inst Ind Sci, Tokyo, Japan
[2] Anhui Univ Finance & Econ, Coll Stat & Appl Math, Bengbu, Anhui, Peoples R China
[3] Chinese Acad Sci, CAS Ctr Excellence Mol Cell Sci, Key Lab Syst Biol,Shanghai Inst Biol Sci, Inst Biochem & Cell Biol,Innovat Ctr Cell Signal, Shanghai, Peoples R China
[4] Shandong Univ Weihai, Sch Math & Stat, Weihai, Peoples R China
[5] South China Univ Technol, Sch Math, Guangzhou, Guangdong, Peoples R China
[6] ShanghaiTech Univ, Sch Life Sci & Technol, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
CELL LUNG-CANCER; BETA-III-TUBULIN; COLORECTAL-CANCER; GENE-EXPRESSION; POOR-PROGNOSIS; FIBRONECTIN; PANCREATIC-CANCER; GASTRIC-CANCER; METASTASIS; PROGRESSION;
D O I
10.1371/journal.pcbi.1005633
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Dynamic network biomarkers (DNB) can identify the critical state or tipping point of a disease, thereby predicting rather than diagnosing the disease. However, it is difficult to apply the DNB theory to clinical practice because evaluating DNB at the critical state required the data of multiple samples on each individual, which are generally not available, and thus limit the applicability of DNB. In this study, we developed a novel method, i.e., single-sample DNB (sDNB), to detect early-warning signals or critical states of diseases in individual patients with only a single sample for each patient, thus opening a new way to predict diseases in a personalized way. In contrast to the information of differential expressions used in traditional biomarkers to "diagnose disease", sDNB is based on the information of differential associations, thereby having the ability to "predict disease" or "diagnose near-future disease". Applying this method to datasets for influenza virus infection and cancer metastasis led to accurate identification of the critical states or correct prediction of the immediate diseases based on individual samples. We successfully identified the critical states or tipping points just before the appearance of disease symptoms for influenza virus infection and the onset of distant metastasis for individual patients with cancer, thereby demonstrating the effectiveness and efficiency of our method for quantifying critical states at the single-sample level.
引用
收藏
页数:21
相关论文
共 65 条
[1]  
[Anonymous], DIS MARKERS
[2]  
[Anonymous], 2011, BASIC STAT ANAL
[3]   HDGF: a novel jack-of-all-trades in cancer [J].
Bao, Cihang ;
Wang, Jianbo ;
Ma, Wei ;
Wang, Xintong ;
Cheng, Yufeng .
FUTURE ONCOLOGY, 2014, 10 (16) :2675-2685
[4]   Global secretome analysis identifies novel mediators of bone metastasis [J].
Blanco, Mario Andres ;
LeRoy, Gary ;
Khan, Zia ;
Aleckovic, Masa ;
Zee, Barry M. ;
Garcia, Benjamin A. ;
Kang, Yibin .
CELL RESEARCH, 2012, 22 (09) :1339-1355
[5]   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
[6]   A Collagen-Remodeling Gene Signature Regulated by TGF-β Signaling Is Associated with Metastasis and Poor Survival in Serous Ovarian Cancer [J].
Cheon, Dong-Joo ;
Tong, Yunguang ;
Sim, Myung-Shin ;
Dering, Judy ;
Berel, Dror ;
Cui, Xiaojiang ;
Lester, Jenny ;
Beach, Jessica A. ;
Tighiouart, Mourad ;
Walts, Ann E. ;
Karlan, Beth Y. ;
Orsulic, Sandra .
CLINICAL CANCER RESEARCH, 2014, 20 (03) :711-723
[7]   Molecular Origins of Cancer Molecular Basis of Metastasis [J].
Chiang, Anne C. ;
Massague, Joan .
NEW ENGLAND JOURNAL OF MEDICINE, 2008, 359 (26) :2814-2823
[8]   Lipase member H is a novel secreted protein associated with a poor prognosis for breast cancer patients [J].
Cui, Meizi ;
Jin, Haofan ;
Shi, Xiumin ;
Qu, Ge ;
Liu, Lidi ;
Ding, Xiaobo ;
Wang, Yanbo ;
Niu, Chao .
TUMOR BIOLOGY, 2014, 35 (11) :11461-11465
[9]   A gene expression signature that defines breast cancer metastases [J].
Ellsworth, Rachel E. ;
Seebach, Jeff ;
Field, Lori A. ;
Heckman, Caroline ;
Kane, Jennifer ;
Hooke, Jeffrey A. ;
Love, Brad ;
Shriver, Craig D. .
CLINICAL & EXPERIMENTAL METASTASIS, 2009, 26 (03) :205-213
[10]   Gene expression analyses of primary melanomas reveal CTHRC1 as an important player in melanoma progression [J].
Eriksson, Johanna ;
Le Joncour, Vadim ;
Nummela, Pirjo ;
Jahkola, Tiina ;
Virolainen, Susanna ;
Laakkonen, Pirjo ;
Saksela, Olli ;
Holtta, Erkki .
ONCOTARGET, 2016, 7 (12) :15065-15092