Therapeutic potential of phosphatidylinositol 3-kinase inhibitors in inflammatory respiratory disease

被引:129
作者
Ito, Kazuhiro
Caramori, Gaetano
Adcock, Ian M.
机构
[1] Imperial Coll London, Cell & Mol Biol Grp, Airways Dis Sect, Natl Heart & Lung Inst, London SW3 6LY, England
[2] Univ Ferrara, Ctr Ric Asma & BPCO, I-44100 Ferrara, Italy
基金
英国医学研究理事会; 英国惠康基金;
关键词
D O I
10.1124/jpet.106.111674
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The phosphoinositide 3-kinase(s) (PI3K) are a family of proteins that catalyze the phosphorylation of the 3-OH position of phosphoinositides and generate lipids that control a wide variety of intracellular signaling pathways. They are classified into three families according to their structure and substrate specificity and are thought to have distinct biological roles. Recent studies suggested that numerous components of the PI3K pathway play a crucial role in the expression and activation of inflammatory mediators, inflammatory cell recruitment, immune cell function, airway remodeling, and corticosteroid insensitivity in chronic inflammatory respiratory disease. Selective PI3K inhibitors have been developed that reduce inflammation and some characteristics of disease in experimental animal models. Targeting specific PI3K isoforms that may be overexpressed or overactive in disease should allow for selective treatment of respiratory diseases. Encouraging data from animal models, primary cells and clinical studies in other diseases suggest that inhibitors of PI3K/Akt may prove to be useful novel therapies in the treatment of asthma and chronic obstructive pulmonary disease.
引用
收藏
页码:1 / 8
页数:8
相关论文
共 43 条
[1]   RETRACTED: Kinase inhibitors and airway inflammation (Retracted article. See vol. 683, pg. 340, 2012) [J].
Adcock, IM ;
Chung, KF ;
Caramori, G ;
Ito, K .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2006, 533 (1-3) :118-132
[2]   Essential role for the p110δ phosphoinositide 3-kinase in the allergic response [J].
Ali, K ;
Bilancio, A ;
Thomas, M ;
Pearce, W ;
Gilfillan, AM ;
Tkaczyk, C ;
Kuehn, N ;
Gray, A ;
Giddings, J ;
Peskett, E ;
Fox, R ;
Bruce, I ;
Walker, C ;
Sawyer, C ;
Okkenhaug, K ;
Finan, P ;
Vanhaesebroeck, B .
NATURE, 2004, 431 (7011) :1007-1011
[3]   COPD - a neglected disease [J].
Barnes, PJ ;
Kleinert, S .
LANCET, 2004, 364 (9434) :564-565
[4]   New concepts in chronic obstructive pulmonary disease [J].
Barnes, PJ .
ANNUAL REVIEW OF MEDICINE, 2003, 54 :113-129
[5]   Chronic obstructive pulmonary disease: molecular and cellular mechanisms [J].
Barnes, PJ ;
Shapiro, SD ;
Pauwels, RA .
EUROPEAN RESPIRATORY JOURNAL, 2003, 22 (04) :672-688
[6]   Protection of human vascular smooth muscle cells from H2O2-induced apoptosis through functional codependence between HO-1 and AKT [J].
Brunt, Keith R. ;
Fenrich, Keith K. ;
Kiani, Gholam ;
Tse, M. Yat ;
Pang, Stephen C. ;
Ward, Christopher A. ;
Melo, Luis G. .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2006, 26 (09) :2027-2034
[7]   Blockade of PI3Kγ suppresses joint inflammation and damage in mouse models of rheumatoid arthritis [J].
Camps, M ;
Rückle, T ;
Ji, H ;
Ardissone, V ;
Rintelen, F ;
Shaw, J ;
Ferrandi, C ;
Chabert, C ;
Gillieron, C ;
Françon, B ;
Martin, T ;
Gretener, D ;
Perrin, D ;
Leroy, D ;
Vitte, PA ;
Hirsch, E ;
Wymann, MP ;
Cirillo, R ;
Schwarz, MK ;
Rommel, C .
NATURE MEDICINE, 2005, 11 (09) :936-943
[8]   Chemokine signalling: pivoting around multiple phosphoinositide 3-kinases [J].
Curnock, AP ;
Logan, MK ;
Ward, SG .
IMMUNOLOGY, 2002, 105 (02) :125-136
[9]   Defective dendritic cell migration and activation of adaptive immunity in PI3Kγ-deficient mice [J].
Del Prete, A ;
Vermi, W ;
Dander, E ;
Otero, K ;
Barberis, L ;
Luini, W ;
Bernasconi, S ;
Sironi, M ;
Santoro, A ;
Garlanda, C ;
Facchetti, F ;
Wymann, MP ;
Vecchi, A ;
Hirsch, E ;
Mantovani, A ;
Sozzani, S .
EMBO JOURNAL, 2004, 23 (17) :3505-3515
[10]   The class II phosphoinositide 3-kinase PI3K-C2β regulates cell migration by a PtdIns(3)P dependent mechanism [J].
Domin, J ;
Harper, L ;
Aubyn, D ;
Wheeler, M ;
Florey, O ;
Haskard, D ;
Yuan, M ;
Zicha, D .
JOURNAL OF CELLULAR PHYSIOLOGY, 2005, 205 (03) :452-462