Cross-talk and modulation of signaling between somatostatin and growth factor receptors

被引:16
作者
Kumar, Ujendra [1 ]
机构
[1] Univ British Columbia, Fac Pharmaceut Sci, Vancouver, BC V6T 1Z3, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
G-protein coupled receptors; Receptor tyrosine kinase; Somatostatin receptors; Signaling; Dimerization; PROTEIN-COUPLED RECEPTORS; BREAST-CANCER CELLS; RESONANCE ENERGY-TRANSFER; EGF-RECEPTOR; TYROSINE PHOSPHORYLATION; ERBB RECEPTORS; RAT PITUITARY; MOLECULAR PHARMACOLOGY; TRASTUZUMAB RESISTANCE; QUANTITATIVE-ANALYSIS;
D O I
10.1007/s12020-011-9524-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The process of homo- and/or heterodimerization of G-protein coupled receptors (GPCRs) and receptor tyrosine kinase (RTK) families are crucial for implicating the fundamental properties of receptor proteins including receptor expression, trafficking, and desensitization as well as signal transduction. The members of GPCR and RTK family constitute largest cell surface receptor proteins and regulate physiological functions of cells in response to external and internal stimuli. Notably, GPCRs and RTKs play major role in regulation of several key cellular functions which are associated with several pathological conditions including cancer biology, neurodegenerative and cardiovascular diseases. The focus of this review is to highlight the recent findings on the possible cross-talk between somatostatin receptors (members of GPCR family) and growth factor receptors like epidermal growth factor receptors (members of RTK family). Furthermore, functional consequences of such an interaction in modulation of signaling pathways linked to pathological conditions specifically in cancer are discussed.
引用
收藏
页码:168 / 180
页数:13
相关论文
共 103 条
[31]   secErbB4-26/549 antagonizes ligand-induced ErbB4 tyrosine phosphorylation [J].
Gilmore, JL ;
Riese, DJ .
ONCOLOGY RESEARCH, 2004, 14 (11-12) :589-602
[32]   Agonist-dependent dissociation of human somatostatin receptor 2 dimers - A role in receptor trafficking [J].
Grant, M ;
Collier, B ;
Kumar, U .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (35) :36179-36183
[33]   The role of subtype-specific ligand binding and the C-tail domain in dimer formation of human somatostatin receptors [J].
Grant, M ;
Patel, RC ;
Kumar, U .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (37) :38636-38643
[34]   Cell growth inhibition and functioning of human somatostatin receptor type 2 are modulated by receptor heterodimerization [J].
Grant, Michael ;
Alturaihi, Haydar ;
Jaquet, Philippe ;
Collier, Brian ;
Kumar, Ujendra .
MOLECULAR ENDOCRINOLOGY, 2008, 22 (10) :2278-2292
[35]   The role of G-proteins in the dimerisation of human somatostatin receptor types 2 and 5 [J].
Grant, Michael ;
Kumar, Ujendra .
REGULATORY PEPTIDES, 2010, 159 (1-3) :3-8
[36]   Experimental evidence for lack of homodimerization of the G protein-coupled human N-formyl peptide receptor [J].
Gripentrog, JM ;
Kantele, KP ;
Jesaitis, AJ ;
Miettinen, HM .
JOURNAL OF IMMUNOLOGY, 2003, 171 (06) :3187-3193
[37]   INSECT CELL-EXPRESSED P180(ERBB3) POSSESSES AN IMPAIRED TYROSINE KINASE-ACTIVITY [J].
GUY, PM ;
PLATKO, JV ;
CANTLEY, LC ;
CERIONE, RA ;
CARRAWAY, KL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (17) :8132-8136
[38]   Epidermal growth factor receptors: critical mediators of multiple receptor pathways [J].
Hackel, PO ;
Zwick, E ;
Prenzel, N ;
Ullrich, A .
CURRENT OPINION IN CELL BIOLOGY, 1999, 11 (02) :184-189
[39]   GPCR-induced migration of breast carcinoma cells depends on both EGFR signal transactivation and EGFR-independent pathways [J].
Hart, S ;
Fischer, OM ;
Prenzel, N ;
Zwick-Wallasch, E ;
Schneider, M ;
Hennighausen, L ;
Ullrich, A .
BIOLOGICAL CHEMISTRY, 2005, 386 (09) :845-855
[40]   Influence of the somatostatin receptor sst2 on growth factor signal cascades in human glioma cells [J].
Held-Feindt, J ;
Forstreuter, F ;
Pufe, T ;
Mentlein, R .
MOLECULAR BRAIN RESEARCH, 2001, 87 (01) :12-21