Abstract |
The human epidermal growth factor ( EGF) receptor (HER) family of receptor tyrosine kinases has frequently been implicated in cancer. Apart from overexpression or mutation of these receptors, also the aberrant autocrine or paracrine activation of HERs by EGF-like ligands may be important in cancer progression. Neuregulins constitute a family of EGF-like ligands that bind to HER3 or HER4, preferably forming heterodimers with the orphan receptor HER2. Mesenchymal neuregulin typically serves as a pro-survival and pro-differentiation signal for adjacent epithelia. Disruption of the balance between proliferation and differentiation, because of autocrine production by the epithelial cells, increased sensitivity to paracrine signals or disruption of the spatial organization, may lead to constitutive receptor activation, in the absence of receptor overexpression. Consequently, the analysis of ligand expression and/or activated receptors in tumor samples may broaden the group of patients that can benefit from targeted therapies.
|
Authors | Christophe Stove, Marc Bracke |
Journal | Clinical & experimental metastasis
(Clin Exp Metastasis)
Vol. 21
Issue 8
Pg. 665-84
( 2004)
ISSN: 0262-0898 [Print] Netherlands |
PMID | 16035612
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)
|
Chemical References |
- Ligands
- Neuregulins
- ErbB Receptors
|
Topics |
- Animals
- ErbB Receptors
(physiology)
- Humans
- Ligands
- Neoplasms
(metabolism)
- Neuregulins
(physiology)
- Signal Transduction
|