The Epidermal growth factor receptor (EGFR) belongs to
the ERBB family of receptor tyrosine kinases, which consists of four closely related
members: EGFR and v-erb-b2 erythroblastic leukemia viral
oncogene homolog 2, neuro/glioblastoma derived oncogene homolog
(ERBB2), ERBB3 and ERBB4. These receptors couple binding of
extracellular growth factor ligands to intracellular signaling pathways and regulate
diverse biologic responses, including proliferation, differentiation, cell motility, and
survival [1].
Six EGFR ligands have been identified including Epidermal growth factor
(EGF), Amphiregulin, TGF-alpha; Betacellulin, HB-EGF
(heparin binding EGF-like growth factor), and Epiregulin [2].
ERBB2is a unique member of the ERBB family in that it
does not bind any of the known ligands with high affinity, but it is the preferred
heterodimeric partner for other EGFR [1].
The ligand-induced receptor dimerization and subsequent autophosphorylation of
distinct tyrosine residues creates docking sites for various membrane-targeted proteins,
including adaptor proteins Growth factor receptor-bound protein 2
(Grb2), Cas-Br-M (murine)
ecotropic retroviral transforming sequence (c-Cbl),
GRB2-associated binding protein 1 (GAB1), SHC (Src homology
2 domain containing) transforming protein 1 (Shc), Docking
protein 2, 56kDa (DOK2), and Epidermal growth factor
receptor pathway substrate 8
(EPS8). Adaptor proteins
mediate various signaling cascades, initiated by EGFR.
A set of cascades are mediated by small GTPases. One such pathway leads to MAP kinase
activation. This pathway involves Shc,
Grb2, Son of Sevenless homologs
(SOS), Harvey rat sarcoma viral oncogene homolog
(H-Ras), Neuroblastoma RAS viral (v-ras) oncogene homolog
(N-Ras), v-Ki-ras2 Kirsten rat sarcoma viral oncogene
homolog (K-Ras).
Adaptors Shc and Grb2
recruit exchange factors on of SOS, forming protein complex
consisting of
Shc/Grb2/SOS.
Activated SOS activates small GTPases H-RAS,
N-RAS, K-RAS by convertingit from inactive GDP-bound state to active
GTP-bound state. Activated RAS-proteins stimulate v-raf-1
murine leukemia viral oncogene homolog 1 (c-Raf-1)/
Mitogen-activated protein kinase kinases 1 and 2 (MEK1(MAP2K1)
MEK2(MAP2K2))/ Mitogen-activated protein
kinase 1-3 (ERK1/2) cascade, which lead to activation
transcription factors ELK1, member of ETS oncogene family
(Elk-1), v-myc myelocytomatosis viral oncogene homolog
(c-Myc), v-fos FBJ murine osteosarcoma viral oncogene
homolog (c-Fos) [3].
The adaptor DOK2 associates with the GTPase-activating
protein RAS p21 protein activator (GTPase activating protein) 1
(p120GAP), which reinforces intrinsic GTPase activity of
RAS-proteins, thereby inactivating them. Thus DOK2 could
attenuate EGF-stimulated mitogen-activated protein (MAP)
kinase activation [4].
Another pathway involving the Ras-related C3 botulinum toxin substrate 1
(Rac1), includes mitogen-induced cytoskeletal changes and
Mitogen-activated protein kinases 8-10 (JNK(MAPK8-10)).
EPS8 is a substrate of the
EGFR. EPS8 complexes with
SOS by the Abl-interactor 1
(E3b1(ABI-1)) and mediates activation of
Rac1.
EGFRs regulate their own internalization via GTP-binding
proteins Rab-family. EPS8 interacts with USP6 N-terminal
like (RNTRE), which is a RAB5A,
member RAS oncogene family (Rab-5A) GTPase-activating
protein. By entering in a complex with EPS8,
RNTRE acts on Rab-5A and
inhibits internalization of the EGFR. Furthermore,
RNTRE diverts EPS8 from its
Rac-activating function, resulting in the attenuation of Rac signaling. Thus, depending
on its state of association with E3b1(ABI-1) or
RNTRE, EPS8 participates in
both EGFR signaling through Rac1, and trafficking through
Rab-5A [5].
Another pathway mediated by Rac1 activation includes the
activation of the Phosphatidylinositol 3-kinase (PI3K) cascade.
EGF stimulation induces association of
c-Cbl, complexed to the adapter protein
Grb2, with Phosphoinositide-3-kinase, regulatory
(PI3K reg class IA) thereby activating
Phosphoinositide-3-kinase catalytic subunit (PI3K cat class
IA) [6].
Activated PI3K cat class IA converts inositol
4,5-biphosphate
(PtdIns(4,5)P2)
into inositol
3,4,5-trisphosphate
(PtdIns(3,4,5)P3), which is a secondary
messenger involved in regulation various processes [7].
PtdIns(3,4,5)P3 associates with the inner lipid bilayer of
the plasma membrane promoting the recruitment of proteins with pleckstrin homology (PH)
domains, including the Vav 2 guanine nucleotide exchange factor
(VAV-2), which activates the
Rho family of Ras-related GTPases, such as Rac1 [8].