Discovery of a Potential Plasma Protein Biomarker Panel for Acute-on-Chronic Liver Failure Induced by Hepatitis B Virus.
Discovery of a Potential Plasma Protein Biomarker Panel for Acute-on-Chronic Liver Failure Induced by Hepatitis B Virus.
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发现乙型肝炎病毒引起的慢性急性肝衰竭的潜在血浆蛋白生物标志物组
DOI:
10.3389/fphys.2017.01009
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发表时间:
2017
影响因子:
4
通讯作者:
Zhu J
中科院分区:
文献类型:
--
作者:
Zhou N;Wang K;Fang S;Zhao X;Huang T;Chen H;Yan F;Tang Y;Zhou H;Zhu J
Hepatitis B virus (HBV)-associated acute-on-chronic liver failure (HBV-ACLF), characterized by an acute deterioration of liver function in the patients with chronic hepatitis B (CHB), is lack of predicting biomarkers for prognosis. Plasma is an ideal sample for biomarker discovery due to inexpensive and minimally invasive sampling and good reproducibility. In this study, immuno-depletion of high-abundance plasma proteins followed by iTRAQ-based quantitative proteomic approach was employed to analyze plasma samples from 20 healthy control people, 20 CHB patients and 20 HBV-ACLF patients, respectively. As a result, a total of 427 proteins were identified from these samples, and 42 proteins were differentially expressed in HBV-ACLF patients as compared to both CHB patients and healthy controls. According to bioinformatics analysis results, 6 proteins related to immune response (MMR), inflammatory response (OPN, HPX), blood coagulation (ATIII) and lipid metabolism (APO-CII, GP73) were selected as biomarker candidates. Further ELISA analysis confirmed the significant up-regulation of GP73, MMR, OPN and down-regulation of ATIII, HPX, APO-CII in HBV-ACLF plasma samples (p < 0.01). Moreover, receiver operating characteristic (ROC) curve analysis revealed high diagnostic value of these candidates in assessing HBV-ACLF. In conclusion, present quantitative proteomic study identified 6 novel HBV-ACLF biomarker candidates and might provide fundamental information for development of HBV-ACLF biomarker.
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DOI:
10.1158/1940-6207.capr-15-0434
发表时间:
2016-09
期刊:
Cancer prevention research (Philadelphia, Pa.)
影响因子:
--
作者:
Duarte-Salles T;Misra S;Stepien M;Plymoth A;Muller D;Overvad K;Olsen A;Tjønneland A;Baglietto L;Severi G;Boutron-Ruault MC;Turzanski-Fortner R;Kaaks R;Boeing H;Aleksandrova K;Trichopoulou A;Lagiou P;Bamia C;Pala V;Palli D;Mattiello A;Tumino R;Naccarati A;Bueno-de-Mesquita HB;Peeters PH;Weiderpass E;Quirós JR;Agudo A;Sánchez-Cantalejo E;Ardanaz E;Gavrila D;Dorronsoro M;Werner M;Hemmingsson O;Ohlsson B;Sjöberg K;Wareham NJ;Khaw KT;Bradbury KE;Gunter MJ;Cross AJ;Riboli E;Jenab M;Hainaut P;Beretta L
通讯作者:
Beretta L
影响因子:
48
作者:
Geiger, Tamar;Cox, Juergen;Mann, Matthias
通讯作者:
Mann, Matthias
影响因子:
13.5
作者:
KOBAYASHI, J;YAMADA, S;KAWASAKI, H
通讯作者:
KAWASAKI, H
影响因子:
3.4
作者:
He, QY;Lau, GKK;Chiu, JF
通讯作者:
Chiu, JF
DOI:
10.1111/j.1440-1746.1997.tb00351.x
发表时间:
1997-01-01
影响因子:
4.1
作者:
Castelino, DJ;Salem, HH
通讯作者:
Salem, HH