A potential role for imatinib and other small molecule tyrosine kinase inhibitors in the treatment of systemic and localized sclerosis

被引:25
作者
Bibi, Yuval [1 ,2 ]
Gottlieb, Alice B. [2 ]
机构
[1] Boston Univ, Med Ctr Tufts NEMC, Sch Med, Dept Dermatol, Boston, MA 02118 USA
[2] Tufts Univ, Sch Med, Boston, MA 02111 USA
关键词
D O I
10.1016/j.jaad.2008.04.034
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Small molecule tyrosine kinase (TK) inhibitor, Such as imatinib, is well established in the treatment of malignancy. Oral administration, high efficacy, and an excellent safety profile have made imatinib a drug of choice for several malignancies and benign conditions. Recent progress in the understanding of several benign conditions has led to the use of TK inhibitors in the treatment of hypereosinophilic syndrome and mastocytosis. Systemic sclerosis (SS) is a recalcitrant disease featuring multiorgan fibrosis and dysfunction. Molecular and biological evidence point to a central role for platelet-derived growth factor receptor, a TK-associated entity, in the pathogenesis of SS. The ability of several TK inhibitors, namely imatinib, to abrogate the activation of platelet-derived growth factor receptor-TK may entail their use in the treatment of SS and possibly more limited forms of sclerosis. Several human studies aiming to examine the use Of imatinib in the treatment of SS are Currently underway.
引用
收藏
页码:654 / 658
页数:5
相关论文
共 42 条
[1]   Inhibition of platelet-derived growth factor signaling attenuates pulmonary fibrosis [J].
Abdollahi, A ;
Li, ML ;
Ping, G ;
Plathow, C ;
Domhan, S ;
Kiessling, F ;
Lee, LB ;
McMahon, G ;
Gröne, HJ ;
Lipson, KE ;
Huber, PE .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 201 (06) :925-935
[2]   Imatinib as a novel antifibrotic agent in bleomycin-induced pulmonary fibrosis in mice [J].
Aono, Y ;
Nishioka, Y ;
Inayama, M ;
Ugai, M ;
Kishi, J ;
Uehara, H ;
Izumi, K ;
Sone, S .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2005, 171 (11) :1279-1285
[3]   Response of idiopathic hypereosinophilic syndrome to treatment with imatinib mesylate [J].
Ault, P ;
Cortes, J ;
Koller, C ;
Kaled, ES ;
Kantarjian, H .
LEUKEMIA RESEARCH, 2002, 26 (09) :881-884
[4]   The efficacy of imatinib mesylate in patients with FIP1L1-PDGFRα-positive hypereosinophilic syndrome. Results of a multicenter prospective study [J].
Baccarani, Michele ;
Cilloni, Daniela ;
Rondoni, Michela ;
Ottaviani, Emanuela ;
Messa, Francesca ;
Merante, Serena ;
Tiribelli, Mario ;
Buccisano, Francesco ;
Testoni, Nicoletta ;
Gottardi, Enrico ;
de Vivo, Antonio ;
Giugliano, Emilia ;
Iacobucci, Ilaria ;
Paolini, Stefania ;
Soverini, Simona ;
Rosti, Gianantonio ;
Rancati, Francesca ;
Astolfi, Cinzia ;
Pane, Fabrizio ;
Saglio, Giuseppe ;
Martinelli, Giovanni .
HAEMATOLOGICA, 2007, 92 (09) :1173-1179
[5]  
Baroni SS, 2006, NEW ENGL J MED, V354, P2667
[6]  
Buchdunger E, 2000, J PHARMACOL EXP THER, V295, P139
[7]   A tyrosine kinase created by fusion of the PDGFRA and FIP1L1 genes as a therapeutic target of imatinib in idiopathic hypereosinophilic syndrome [J].
Cools, J ;
DeAngelo, DJ ;
Gotlib, J ;
Stover, EH ;
Legare, RD ;
Cortes, J ;
Kutok, J ;
Clark, J ;
Galinsky, I ;
Griffin, JD ;
Cross, NCP ;
Tefferi, A ;
Malone, J ;
Alam, R ;
Schrier, SL ;
Schmid, J ;
Rose, M ;
Vandenberghe, P ;
Verhoef, G ;
Boogaerts, M ;
Wlodarska, I ;
Kantarjian, H ;
Marynen, P ;
Coutre, SE ;
Stone, R ;
Gilliland, DG .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (13) :1201-1214
[8]   Practical management of patients with chronic myeloid leukemia receiving imatinib [J].
Deininger, MWN ;
O'Brien, SG ;
Ford, JM ;
Druker, BJ .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (08) :1637-1647
[9]   Imatinib mesylate reduces production of extracellular matrix and prevents development of experimental dermal fibrosis [J].
Distler, Joerg H. W. ;
Juengel, Astrid ;
Huber, Lars C. ;
Schulze-Horsel, Ursula ;
Zwerina, Jochen ;
Gay, Renate E. ;
Michel, Beat A. ;
Hauser, Thomas ;
Schett, Georg ;
Gay, Steffen ;
Distler, Oliver .
ARTHRITIS AND RHEUMATISM, 2007, 56 (01) :311-322
[10]   Effects of a selective inhibitor of the Abl tyrosine kinase on the growth of Bcr-Abl positive cells [J].
Druker, BJ ;
Tamura, S ;
Buchdunger, E ;
Ohno, S ;
Segal, GM ;
Fanning, S ;
Zimmermann, J ;
Lydon, NB .
NATURE MEDICINE, 1996, 2 (05) :561-566