Plasma protein profiling in patients undergoing coronary artery bypass grafting surgery and clinical significance
This study was designed to identify the protein profiling in patients with triple vessel coronary artery disease (CAD) undergoing CABG, in order to detect CAD-related differential proteins in these patients. CABG patients with triple vessel disease with/without left main stenosis ( =160) were compar...
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Published in | Oncotarget Vol. 8; no. 36; pp. 60528 - 60538 |
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Abstract | This study was designed to identify the protein profiling in patients with triple vessel coronary artery disease (CAD) undergoing CABG, in order to detect CAD-related differential proteins in these patients. CABG patients with triple vessel disease with/without left main stenosis (
=160) were compared to normal coronary angiographic subjects (
=160). Plasma samples of 20 males and 20 females in each group were analyzed with iTRAQ technique. ELISA test was used to test the chosen proteins from iTRAQ results in plasma samples from a new cohort of the CABG group (
=120, male/femal=61/59) and control (
=120, male/female=60/60). iTRAQ detected 544 proteins with 35 up-regulated and 41 down-regulated (change fold > 1.2 or < 0.83,
< 0.05). Three proteins including platelet factor 4 (PF4), coagulation factor XIII B chain (F13B), and secreted frizzled-related protein 1 (sFRP1) were selected for validation by using ELISA that demonstrated significant up-regulation of PF4 and sFRP1 (
< 0.05). There was a positive correlation between these proteins and CAD (
< 0.05) and myocardial infarction history (
< 0.05). Thus, we for the first time have found 76 proteins differentially expressed in plasma of CABG patients. The thrombotic disease/inflammation progress-related protein PF4 and sFRP1, a member of the Wnt/fz signal-transduction pathway and related to myocardial repair, are significantly up-regulated in triple-vessel disease with/without left main stenosis. PF4 may be developed as a biomarker for the diagnosis of the severity of CAD requiring CABG procedure. |
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AbstractList | This study was designed to identify the protein profiling in patients with triple vessel coronary artery disease (CAD) undergoing CABG, in order to detect CAD-related differential proteins in these patients. CABG patients with triple vessel disease with/without left main stenosis (
=160) were compared to normal coronary angiographic subjects (
=160). Plasma samples of 20 males and 20 females in each group were analyzed with iTRAQ technique. ELISA test was used to test the chosen proteins from iTRAQ results in plasma samples from a new cohort of the CABG group (
=120, male/femal=61/59) and control (
=120, male/female=60/60). iTRAQ detected 544 proteins with 35 up-regulated and 41 down-regulated (change fold > 1.2 or < 0.83,
< 0.05). Three proteins including platelet factor 4 (PF4), coagulation factor XIII B chain (F13B), and secreted frizzled-related protein 1 (sFRP1) were selected for validation by using ELISA that demonstrated significant up-regulation of PF4 and sFRP1 (
< 0.05). There was a positive correlation between these proteins and CAD (
< 0.05) and myocardial infarction history (
< 0.05). Thus, we for the first time have found 76 proteins differentially expressed in plasma of CABG patients. The thrombotic disease/inflammation progress-related protein PF4 and sFRP1, a member of the Wnt/fz signal-transduction pathway and related to myocardial repair, are significantly up-regulated in triple-vessel disease with/without left main stenosis. PF4 may be developed as a biomarker for the diagnosis of the severity of CAD requiring CABG procedure. This study was designed to identify the protein profiling in patients with triple vessel coronary artery disease (CAD) undergoing CABG, in order to detect CAD-related differential proteins in these patients. CABG patients with triple vessel disease with/without left main stenosis (n =160) were compared to normal coronary angiographic subjects (n =160). Plasma samples of 20 males and 20 females in each group were analyzed with iTRAQ technique. ELISA test was used to test the chosen proteins from iTRAQ results in plasma samples from a new cohort of the CABG group (n=120, male/femal=61/59) and control (n =120, male/female=60/60). iTRAQ detected 544 proteins with 35 up-regulated and 41 down-regulated (change fold > 1.2 or < 0.83, p < 0.05). Three proteins including platelet factor 4 (PF4), coagulation factor XIII B chain (F13B), and secreted frizzled-related protein 1 (sFRP1) were selected for validation by using ELISA that demonstrated significant up-regulation of PF4 and sFRP1 (p < 0.05). There was a positive correlation between these proteins and CAD (p < 0.05) and myocardial infarction history (p < 0.05). Thus, we for the first time have found 76 proteins differentially expressed in plasma of CABG patients. The thrombotic disease/inflammation progress-related protein PF4 and sFRP1, a member of the Wnt/fz signal-transduction pathway and related to myocardial repair, are significantly up-regulated in triple-vessel disease with/without left main stenosis. PF4 may be developed as a biomarker for the diagnosis of the severity of CAD requiring CABG procedure.This study was designed to identify the protein profiling in patients with triple vessel coronary artery disease (CAD) undergoing CABG, in order to detect CAD-related differential proteins in these patients. CABG patients with triple vessel disease with/without left main stenosis (n =160) were compared to normal coronary angiographic subjects (n =160). Plasma samples of 20 males and 20 females in each group were analyzed with iTRAQ technique. ELISA test was used to test the chosen proteins from iTRAQ results in plasma samples from a new cohort of the CABG group (n=120, male/femal=61/59) and control (n =120, male/female=60/60). iTRAQ detected 544 proteins with 35 up-regulated and 41 down-regulated (change fold > 1.2 or < 0.83, p < 0.05). Three proteins including platelet factor 4 (PF4), coagulation factor XIII B chain (F13B), and secreted frizzled-related protein 1 (sFRP1) were selected for validation by using ELISA that demonstrated significant up-regulation of PF4 and sFRP1 (p < 0.05). There was a positive correlation between these proteins and CAD (p < 0.05) and myocardial infarction history (p < 0.05). Thus, we for the first time have found 76 proteins differentially expressed in plasma of CABG patients. The thrombotic disease/inflammation progress-related protein PF4 and sFRP1, a member of the Wnt/fz signal-transduction pathway and related to myocardial repair, are significantly up-regulated in triple-vessel disease with/without left main stenosis. PF4 may be developed as a biomarker for the diagnosis of the severity of CAD requiring CABG procedure. This study was designed to identify the protein profiling in patients with triple vessel coronary artery disease (CAD) undergoing CABG, in order to detect CAD-related differential proteins in these patients. CABG patients with triple vessel disease with/without left main stenosis ( n =160) were compared to normal coronary angiographic subjects ( n =160). Plasma samples of 20 males and 20 females in each group were analyzed with iTRAQ technique. ELISA test was used to test the chosen proteins from iTRAQ results in plasma samples from a new cohort of the CABG group ( n =120, male/femal=61/59) and control ( n =120, male/female=60/60). iTRAQ detected 544 proteins with 35 up-regulated and 41 down-regulated (change fold > 1.2 or < 0.83, p < 0.05). Three proteins including platelet factor 4 (PF4), coagulation factor XIII B chain (F13B), and secreted frizzled-related protein 1 (sFRP1) were selected for validation by using ELISA that demonstrated significant up-regulation of PF4 and sFRP1 ( p < 0.05). There was a positive correlation between these proteins and CAD ( p < 0.05) and myocardial infarction history ( p < 0.05). Thus, we for the first time have found 76 proteins differentially expressed in plasma of CABG patients. The thrombotic disease/inflammation progress-related protein PF4 and sFRP1, a member of the Wnt/fz signal-transduction pathway and related to myocardial repair, are significantly up-regulated in triple-vessel disease with/without left main stenosis. PF4 may be developed as a biomarker for the diagnosis of the severity of CAD requiring CABG procedure. |
Author | Guo, Zhi-Peng Song, Zhen-Guo Liu, Xiao-Cheng Jing, Rui He, Guo-Wei Hou, Hai-Tao |
AuthorAffiliation | 5 Medical College, Zhejiang University, Zhejiang, China 4 The Heart Center, The Affiliated Hospital of Hangzhou Normal University, Hangzhou, China 1 Center for Basic Medical Research, TEDA International Cardiovascular Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing Shi, China 2 Department of Cardiovascular Surgery, TEDA International Cardiovascular Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing Shi, China 6 Department of Surgery, Oregon Health & Science University, Portland, OR, USA 3 Department of Cardiology, TEDA International Cardiovascular Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing Shi, China |
AuthorAffiliation_xml | – name: 2 Department of Cardiovascular Surgery, TEDA International Cardiovascular Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing Shi, China – name: 1 Center for Basic Medical Research, TEDA International Cardiovascular Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing Shi, China – name: 6 Department of Surgery, Oregon Health & Science University, Portland, OR, USA – name: 3 Department of Cardiology, TEDA International Cardiovascular Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing Shi, China – name: 4 The Heart Center, The Affiliated Hospital of Hangzhou Normal University, Hangzhou, China – name: 5 Medical College, Zhejiang University, Zhejiang, China |
Author_xml | – sequence: 1 givenname: Zhi-Peng surname: Guo fullname: Guo, Zhi-Peng organization: Center for Basic Medical Research, TEDA International Cardiovascular Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing Shi, China, Department of Cardiovascular Surgery, TEDA International Cardiovascular Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing Shi, China – sequence: 2 givenname: Hai-Tao surname: Hou fullname: Hou, Hai-Tao organization: Center for Basic Medical Research, TEDA International Cardiovascular Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing Shi, China – sequence: 3 givenname: Rui surname: Jing fullname: Jing, Rui organization: Department of Cardiology, TEDA International Cardiovascular Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing Shi, China – sequence: 4 givenname: Zhen-Guo surname: Song fullname: Song, Zhen-Guo organization: Department of Cardiology, TEDA International Cardiovascular Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing Shi, China – sequence: 5 givenname: Xiao-Cheng surname: Liu fullname: Liu, Xiao-Cheng organization: Department of Cardiovascular Surgery, TEDA International Cardiovascular Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing Shi, China – sequence: 6 givenname: Guo-Wei surname: He fullname: He, Guo-Wei organization: Center for Basic Medical Research, TEDA International Cardiovascular Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing Shi, China, Department of Cardiovascular Surgery, TEDA International Cardiovascular Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing Shi, China, The Heart Center, The Affiliated Hospital of Hangzhou Normal University, Hangzhou, China, Medical College, Zhejiang University, Zhejiang, China, Department of Surgery, Oregon Health & Science University, Portland, OR, USA |
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CitedBy_id | crossref_primary_10_3389_fcvm_2022_960105 crossref_primary_10_1088_1758_5090_acb1da crossref_primary_10_1177_0300060518793787 crossref_primary_10_1002_jcp_27433 crossref_primary_10_1016_j_jtcvs_2020_01_079 crossref_primary_10_62347_QSRI6160 crossref_primary_10_3892_etm_2018_6879 |
Cites_doi | 10.1002/pmic.200401308 10.1073/pnas.231619298 10.3389/fphys.2012.00001 10.1074/mcp.R200007-MCP200 10.1016/S0925-4773(99)00236-1 10.1159/000381259 10.1039/C5NR02132D 10.1002/prca.201400166 10.1161/HYPERTENSIONAHA.109.141127 10.1016/S0735-1097(02)02868-1 10.1074/jbc.M208894200 10.1002/elps.201000171 10.1038/srep36541 10.1371/journal.pone.0072111 10.1007/BF02905035 10.2353/ajpath.2008.070130 10.1016/j.athoracsur.2013.11.069 10.1161/01.CIR.97.3.251 10.1111/biom.12107 10.1161/01.CIR.0000039342.85015.5C 10.1016/j.patrec.2005.10.010 10.1021/pr1002017 10.1016/j.ahj.2006.03.007 |
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Keywords | coronary artery disease platelet factor 4 secreted frizzled-related protein 1 coronary artery bypass grafting |
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Title | Plasma protein profiling in patients undergoing coronary artery bypass grafting surgery and clinical significance |
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