Correlation of serpin-protease expression by comparative analysis of real-time PCR profiling data

被引:16
作者
Badola, Sunita
Spurling, Heidi
Robison, Keith
Fedyk, Eric R.
Silverman, Gary A.
Strayle, Jochen
Kapeller, Rosana
Tsu, Christopher A.
机构
[1] Millennium Pharmaceut Inc, Cambridge, MA 02139 USA
[2] Univ Pittsburgh, Magee Womens Hosp, Sch Med, Dept Pediat, Pittsburgh, PA 15213 USA
[3] Bayer HealthCare, D-42096 Wuppertal, Germany
关键词
protease; serpin; cancer; imbalance; expression profiling; gene correlation; PCR;
D O I
10.1016/j.ygeno.2006.03.017
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Imbalanced protease activity has long been recognized in the progression of disease states such as cancer and inflammation. Serpins, the largest family of endogenous protease inhibitors, target a wide variety of serine and cysteine proteases and play a role in a number of physiological and pathological states. The expression profiles of 20 serpins and 105 serine and cysteine proteases were determined across a panel of normal and diseased human tissues. In general, expression of serpins was, highly restricted in both normal and diseased tissues, suggesting defined physiological roles for these protease inhibitors. A high correlation in expression for a particular serpin-protease pair in healthy tissues was often predictive of a biological interaction. The most striking finding was the dramatic change observed in the regulation of expression between proteases and their cognate inhibitors in diseased tissues. The loss of regulated serpin-protease matched expression may underlie the imbalanced protease activity observed in pathological states. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:173 / 184
页数:12
相关论文
共 58 条
[1]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[2]  
BALOW RM, 1986, J BIOL CHEM, V261, P2409
[3]  
Barrett AJ, 2004, CURR OPIN DRUG DISC, V7, P334
[4]   In vitro elucidation of substrate specificity and bioassay of proprotein convertase 4 using intrarnolecularly quenched fluorogenic peptides [J].
Basak, S ;
Chrétien, M ;
Mbikay, M ;
Basak, A .
BIOCHEMICAL JOURNAL, 2004, 380 :505-514
[5]  
Bassi DE, 2000, MOL CARCINOGEN, V28, P63, DOI 10.1002/1098-2744(200006)28:2<63::AID-MC1>3.3.CO
[6]  
2-3
[7]   Prediction of complete gene structures in human genomic DNA [J].
Burge, C ;
Karlin, S .
JOURNAL OF MOLECULAR BIOLOGY, 1997, 268 (01) :78-94
[8]   d2_cluster: A validated method for clustering EST and full-length cDNA sequences [J].
Burke, J ;
Davison, D ;
Hide, W .
GENOME RESEARCH, 1999, 9 (11) :1135-1142
[9]   Co-expression of the squamous cell carcinoma antigens 1 and 2 in normal adult human tissues and squamous cell carcinomas [J].
Cataltepe, S ;
Gornstein, ER ;
Schick, C ;
Kamachi, Y ;
Chatson, K ;
Fries, J ;
Silverman, GA ;
Upton, MP .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2000, 48 (01) :113-122
[10]   Protease injury in the development of COPD - Thomas A. Neff Lecture [J].
Chapman, HA ;
Shi, GP .
CHEST, 2000, 117 (05) :295S-298S