Serum cyclin-dependent kinase 9 is a potential biomarker of atherosclerotic inflammation

被引:15
作者
Han, Yeming [1 ,2 ]
Zhao, Shanshan [3 ]
Gong, Yaoqin [3 ,4 ]
Hou, Guihua [3 ]
Li, Xi [3 ,4 ]
Li, Li [1 ,2 ]
机构
[1] Shandong Univ, Chinese Minist Educ, Key Lab Cardiovasc Remodeling & Funct Res, Jinan 250012, Shandong, Peoples R China
[2] Shandong Univ, Qilu Hosp, Dept Cardiol, Chinese Minist Hlth, Jinan 250012, Shandong, Peoples R China
[3] Shandong Univ, Sch Med, Minist Educ, Lab Expt Teratol, Jinan 250012, Shandong, Peoples R China
[4] Shandong Univ, Sch Med, Dept Genet, Jinan 250012, Shandong, Peoples R China
基金
中国国家自然科学基金; 美国国家科学基金会;
关键词
atherosclerosis; inflammation; serum; proteomics; CDK9; RNA-POLYMERASE-II; HEART-FAILURE; P-TEFB; FLAVOPIRIDOL; INHIBITION; CDK9; DIFFERENTIATION; EXPRESSION; THERAPY; COMPLEX;
D O I
10.18632/oncotarget.6443
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Atherosclerotic coronary artery disease (CAD) is one of the most prevalent diseases worldwide. Atherosclerosis was considered to be the single most important contributor to CAD. In this study, a distinct serum protein expression pattern in CAD patients was demonstrated by proteomic analysis with two-dimensional gel electrophoresis coupled with mass spectrometry. In particular, CDK9 was found to be highly elevated in serum, monocytes and artery plaque samples of CAD patients. Furthermore, there was high infiltration of CD14+ monocytes/macrophages within artery plaques correlated with the expression of CDK9. Moreover, Flavopiridol (CDK9 inhibitor) could inhibit THP-1 cell (monocytic acute leukemia cell line) proliferation by targeting CDK9. Altogether, These findings indicate that CDK9 represent an important role for inflammation in the pathogenesis of atherosclerosis. It may be a potential biomarker of atherosclerotic inflammation and offer insights into the pathophysiology and targeted therapy for atherosclerotic CAD.
引用
收藏
页码:1854 / 1862
页数:9
相关论文
共 39 条
[1]   Current role of biomarkers in carotid disease: a systematic review [J].
Avgerinos, Efthimios D. ;
Kadoglou, Nikolaos P. E. ;
Moulakakis, Konstantinos G. ;
Giannakopoulos, Triantafillos G. ;
Liapis, Christos D. .
INTERNATIONAL JOURNAL OF STROKE, 2011, 6 (04) :337-345
[2]  
Bagella L, 2000, J CELL BIOCHEM, V78, P170, DOI 10.1002/(SICI)1097-4644(20000701)78:1<170::AID-JCB16>3.3.CO
[3]  
2-1
[4]   CDK9/CYCLIN T1 expression during normal lymphoid differentiation and malignant transformation [J].
Bellan, C ;
De Falco, G ;
Lazzi, S ;
Micheli, R ;
Vicidomini, S ;
Schürfeld, K ;
Amato, T ;
Palumbo, A ;
Bagella, L ;
Sabattini, E ;
Bartolommei, S ;
Hummel, M ;
Pileri, S ;
Tosi, P ;
Leoncini, L ;
Giordano, A .
JOURNAL OF PATHOLOGY, 2004, 203 (04) :946-952
[5]   Flavopiridol inactivates P-TEFb and blocks most RNA polymerase II transcription in vivo [J].
Chao, SH ;
Price, DH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (34) :31793-31799
[6]   Identification of New Biomarkers of Low-Dose GH Replacement Therapy in GH-Deficient Patients [J].
Cruz-Topete, Diana ;
Jorgensen, Jens Otto L. ;
Christensen, Britt ;
Sackmann-Sala, Lucila ;
Krusenstjerna-Hafstrom, Thomas ;
Jara, Adam ;
Okada, Shigeru ;
Kopchick, John J. .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2011, 96 (07) :2089-2097
[7]  
de Azevedo WF, 2002, BIOCHEM BIOPH RES CO, V293, P566
[8]  
De Falco G, 2005, CANCER BIOL THER, V4, P277
[9]   Cdk9/Cyclin T1 complex: A key player during the activation/differentiation process of normal lymphoid B cells [J].
De Falco, Giulia ;
Leucci, Eleonora ;
Onnis, Anna ;
Bellan, Cristiana ;
Tigli, Chiara ;
Wirths, Stefan ;
Cerino, Giovanna ;
Cocco, Mario ;
Crupi, Domenica ;
De Luca, Antonio ;
Lanzavecchia, Antonio ;
Tosi, Piero ;
Leoncini, Lorenzo ;
Giordano, Antonio .
JOURNAL OF CELLULAR PHYSIOLOGY, 2008, 215 (01) :276-282
[10]   Cyclin T: Three forms for different roles in physiological and pathological functions [J].
De Luca, A ;
De Falco, M ;
Baldi, A ;
Paggi, MG .
JOURNAL OF CELLULAR PHYSIOLOGY, 2003, 194 (02) :101-107