Biology and impact of signal transducers and activators of transcription and their regulators as targets in cancer therapy

被引:1
作者
Pfitzner, Edith
Nonnenmacher, Frank
Baus, Daniela
机构
[1] Univ Jena, Inst Biochem & Biophys, D-07743 Jena, Germany
[2] Inst Biomed Res, D-60596 Frankfurt, Germany
关键词
STAT; JAK; cancer; cytokine; SOCS; signaling; inhibitors;
D O I
10.2174/157436206778226914
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
While chemo- and radiotherapy is far developed and successfully employed by default for cancer treatment, severe side effects point to the urgent need for more specific therapies based on the molecular mechanisms of this disease. Strategies to specifically inhibit signaling pathways that are known to force proliferation, prevent apoptosis or promote angiogenesis are expected to have a substantial impact on the future direction taken in cancer therapy. The Janus Kinase (JAK) / Signal transducer and activator of transcription (STAT) pathway is one major signaling pathway converting the signal of cytokines, growth factors and hormones into gene expression programs regulating essential cellular functions like proliferation, differentiation and survival. The suppressors of cytokine signaling (SOCS) as well as phosphatases normally tightly regulate the JAK/STAT pathway. Frequently, however this pathway is constitutively activated in a wide variety of human malignancies and substantially contributes to carcinogenesis. Consequently, new strategies for targeting the JAK/STAT pathway have been developed. This review discusses the biology of the JAK/STAT signaling pathway, which offers several molecular strategies for therapeutic interruption.
引用
收藏
页码:337 / 351
页数:15
相关论文
共 231 条
[1]  
Alas S, 2003, CLIN CANCER RES, V9, P316
[2]  
ALEXANDER WS, ROLE SUPPRESSORS CYT
[3]   Identification of a genetic signature of activated signal transducer and activator of transcription 3 in human tumors [J].
Alvarez, JV ;
Febbo, PG ;
Ramaswamy, S ;
Loda, M ;
Richardson, A ;
Frank, DA .
CANCER RESEARCH, 2005, 65 (12) :5054-5062
[4]   RETRACTED: A cytosolic protein-tyrosine phosphatase PTP1B specifically dephosphorylates and deactivates prolactin-activated STAT5a and STAT5b (Retracted Article) [J].
Aoki, N ;
Matsuda, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (50) :39718-39726
[5]   The signal transducer and activator of transcription STAT5b gene is a new partner of retinoic acid receptor α in acute promyelocytic-like leukaemia [J].
Arnould, C ;
Philippe, C ;
Bourdon, V ;
Grégoire, MJ ;
Berger, R ;
Jonveaux, P .
HUMAN MOLECULAR GENETICS, 1999, 8 (09) :1741-1749
[6]   Functionally distinct isoforms of STAT5 are generated by protein processing [J].
Azam, M ;
Lee, C ;
Strehlow, I ;
Schindler, C .
IMMUNITY, 1997, 6 (06) :691-701
[7]   Specific function of STAT3, SOCS1, and SOCS3 in the regulation of proliferation and survival of classical Hodgkin lymphoma cells [J].
Bans, D ;
Pfitzner, E .
INTERNATIONAL JOURNAL OF CANCER, 2006, 118 (06) :1404-1413
[8]   VEGF differentially activates STAT3 in microvascular endothelial cells [J].
Bartoli, M ;
Platt, DH ;
Lemtalsi, T ;
Gu, XL ;
Brooks, SE ;
Marrero, MB ;
Caldwell, RB .
FASEB JOURNAL, 2003, 17 (09) :1562-+
[9]  
Barton BE, 2004, MOL CANCER THER, V3, P11
[10]   Three-dimensional structure of the Stat3β homodimer bound to DNA [J].
Becker, S ;
Groner, B ;
Müller, CW .
NATURE, 1998, 394 (6689) :145-151