An Update on Src Family of Nonreceptor Tyrosine Kinases Biology

被引:64
作者
Espada, J. [1 ,2 ]
Martin-Perez, J. [3 ]
机构
[1] Ramon & Cajal Univ Hosp, Expt Dermatol & Skin Biol Grp, Ramon & Cajal Inst Hlth Res IRYCIS, Colmenar Viejo Rd Km 9,100, Madrid 28034, Spain
[2] Univ Bernardo OHiggins, Bionanotechnol Lab, Gen Gana 1780, Santiago 8370854, Chile
[3] Inst Invest Biomed Alberto Sols CSIC UAM, Dept Canc Biol, Madrid, Spain
来源
INTERNATIONAL REVIEW OF CELL AND MOLECULAR BIOLOGY, VOL 331 | 2017年 / 331卷
关键词
FOCAL ADHESION KINASE; BREAST-CANCER-CELLS; C-SRC; PROLACTIN RECEPTOR; REDOX REGULATION; STEM-CELLS; TRASTUZUMAB RESISTANCE; POTENTIAL TARGET; MESENCHYMAL TRANSITION; MOLECULAR-MECHANISMS;
D O I
10.1016/bs.ircmb.2016.09.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The members of the Src family of nonreceptor tyrosine kinases (SFKs) are implicated in multiple signaling processes that regulate key cellular functions, including proliferation, migration, differentiation, and survival. SFKs are activated by a large number of receptors for growth factors, cytokines, steroid hormones, G protein-coupled receptors, and also by adhesion proteins and other signaling partners. Through their common modular kinase an adapter protein domains, SFKs critically contribute to diversify different signal inputs, weaving a complex and dynamic network of cellular responses. Not surprisingly, SFKs are involved in embryo development and in the maintenance of different adult tissues and organs. Conversely, dysfunction of SFKs is associated with different pathologies, including cancer. Despite the continuous research in the field, several aspects of SFKs regulation and function are still not well defined and new roles for these proteins are steadily reported. The aim of this review is to provide an update on the major regulatory mechanisms of SFKs activity, including the emerging redox-dependent
引用
收藏
页码:83 / 122
页数:40
相关论文
共 185 条
[91]   SIGNALLING SRC and survival [J].
McCarthy, Nicola .
NATURE REVIEWS CANCER, 2012, 12 (02) :81-81
[92]   Src family kinase activity is required for murine embryonic stem cell growth and differentiation [J].
Meyn, MA ;
Schreiner, SJ ;
Dumitrescu, TP ;
Nau, GJ ;
Smithgall, TE .
MOLECULAR PHARMACOLOGY, 2005, 68 (05) :1320-1330
[93]   Chemical Genetics Identifies c-Src as an Activator of Primitive Ectoderm Formation in Murine Embryonic Stem Cells [J].
Meyn, Malcolm A., III ;
Smithgall, Thomas E. .
SCIENCE SIGNALING, 2009, 2 (92) :ra64
[94]   Activation of the Src/p21ras/Erk pathway by progesterone receptor via cross-talk with estrogen receptor [J].
Migliaccio, A ;
Piccolo, D ;
Castoria, G ;
Di Domenico, M ;
Bilancio, A ;
Lombardi, M ;
Gong, WR ;
Beato, M ;
Auricchio, F .
EMBO JOURNAL, 1998, 17 (07) :2008-2018
[95]   Regulation of intracellular signalling through cysteine oxidation by reactive oxygen species [J].
Miki, Hiroaki ;
Funato, Yosuke .
JOURNAL OF BIOCHEMISTRY, 2012, 151 (03) :255-261
[96]   Focal adhesion kinase: In command and control of cell motility [J].
Mitra, SK ;
Hanson, DA ;
Schlaepfer, DD .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2005, 6 (01) :56-68
[97]   PROFOUND BLOCK IN THYMOCYTE DEVELOPMENT IN MICE LACKING P56(LCK) [J].
MOLINA, TJ ;
KISHIHARA, K ;
SIDEROVSKI, DP ;
VANEWIJK, W ;
NARENDRAN, A ;
TIMMS, E ;
WAKEHAM, A ;
PAIGE, CJ ;
HARTMANN, KU ;
VEILLETTE, A ;
DAVIDSON, D ;
MAK, TW .
NATURE, 1992, 357 (6374) :161-164
[98]   MAMMARY-TUMORS EXPRESSING THE NEU PROTOONCOGENE POSSESS ELEVATED C-SRC TYROSINE KINASE-ACTIVITY [J].
MUTHUSWAMY, SK ;
SIEGEL, PM ;
DANKORT, DL ;
WEBSTER, MA ;
MULLER, WJ .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (01) :735-743
[99]  
Nagata Y, 2004, CANCER CELL, V6, P117, DOI 10.1016/j.ccr.2004.06.022
[100]  
NAKAMURA K, 1993, ONCOGENE, V8, P3133