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epiregulin

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epiregulin

A member of the epidermal growth family which is encoded by EREG  on chromosome 4q13.3. It is a ligand of the EGF receptor (EGFR) and ERBB4; it may mediate localised cell proliferation, and may stimulate cell proliferation and/or angiogenesis.
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Moreover, the interactions between KDM2A and BCOR can inhibit osteogenesis by suppressing epiregulin (EREG) gene transcription, which is required for the expression of osterix (OSX) and distalless homeobox 5 (DLX5) [52].
Insulin-like growth factor (IGF-I) has shown promise in animal models and early human studies, promoting cumulus cell expansion [52], and recombinant epidermal growth factor has been added with success to some culture systems [53] as well as its family members amphiregulin and epiregulin showing promise in terms of maturation rates and embryo developmental capacity to the day two to three stage [54].
According to Missiaglia and colleagues [28], microsatellite instable-high (MSI) and BRAF mutation were predominate among proximal (right-sided) tumours, while distal cancers (left-sided) were characterised by chromosome instable, high expression of epiregulin, and human epidermal growth factor receptor 2 (HER2) amplification [24, 29, 30].
The LH stimulation induces a transient sequential expression of epidermal growth factors such as amphiregulin, epiregulin and betacellulin.
For example, the following genes exhibited statistically significant (P<05) modulation early in Zone I and late in Zone II: CDH5, PECAM-1, SERPINF1, TGFBR1, Endothelial cell growth factor-1 (Ecgfl), Endothelial PAS domain protein-1 (Epasl), Epiregulin (Ereg), Interleukin 12a (1112a), Integrin aV (Itgav), Nudix-type motif 6n (Nudt6), and Tumor necrosis factor ligand superfamily member-12 (Tnfsfl2).
Epiregulin belongs to the epidermal growth factor (EGF) family and is produced as a result of activation of nuclear factor jB pathway(NF-jB) which is stimulated by TLR4 (Figure 3).
On the other hand, proliferative or synthetic SMCs show altered protein expression including increased expression of low-molecular weight caldesmon (l-caldesmon), c-fos, Egr-1, epiregulin, and SMemb MHC (Sobue et al.
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