ERBB3

From Wikipedia, the free encyclopedia


V-erb-b2 erythroblastic leukemia viral oncogene homolog 3 (avian)
PDB rendering based on 1m6b.
Available structures: 1m6b
Identifiers
Symbol(s) ERBB3; ErbB-3; HER3; MDA-BF-1; MGC88033; c-erbB-3; c-erbB3; erbB3-S; p180-ErbB3; p45-sErbB3; p85-sErbB3
External IDs OMIM: 190151 MGI95411 HomoloGene20457
RNA expression pattern

More reference expression data

Orthologs
Human Mouse
Entrez 2065 13867
Ensembl ENSG00000065361 ENSMUSG00000018166
Uniprot P21860 O88458
Refseq NM_001005915 (mRNA)
NP_001005915 (protein)
XM_972868 (mRNA)
XP_977962 (protein)
Location Chr 12: 54.76 - 54.78 Mb Chr 10: 127.97 - 127.99 Mb
Pubmed search [1] [2]

V-erb-b2 erythroblastic leukemia viral oncogene homolog 3 (avian), also known as ERBB3, is a human gene.

This gene encodes a member of the epidermal growth factor receptor (EGFR) family of receptor tyrosine kinases. This membrane-bound protein has a neuregulin binding domain but not an active kinase domain. It therefore can bind this ligand but not convey the signal into the cell through protein phosphorylation. However, it does form heterodimers with other EGF receptor family members which do have kinase activity. Heterodimerization leads to the activation of pathways which lead to cell proliferation or differentiation. Amplification of this gene and/or overexpression of its protein have been reported in numerous cancers, including prostate, bladder, and breast tumors. Alternate transcriptional splice variants encoding different isoforms have been characterized. One isoform lacks the intermembrane region and is secreted outside the cell. This form acts to modulate the activity of the membrane-bound form. Additional splice variants have also been reported, but they have not been thoroughly characterized.[1]

It is thought that ERBB3, when activated, becomes a substrate for dimerization and subsequent phosphorylation by ERBB1, ERBB2 and ERBB4.

Like many of the receptor tyrosine-kinases, ERBB3 is activated by extracellular ligand. Ligands known to bind to ERBB3 include heregulin.


[edit] See also

[edit] References

[edit] Further reading

  • Corfas G, Roy K, Buxbaum JD (2004). "Neuregulin 1-erbB signaling and the molecular/cellular basis of schizophrenia.". Nat. Neurosci. 7 (6): 575–80. doi:10.1038/nn1258. PMID 15162166. 
  • Plowman GD, Whitney GS, Neubauer MG, et al. (1990). "Molecular cloning and expression of an additional epidermal growth factor receptor-related gene.". Proc. Natl. Acad. Sci. U.S.A. 87 (13): 4905–9. PMID 2164210. 
  • Kraus MH, Issing W, Miki T, et al. (1990). "Isolation and characterization of ERBB3, a third member of the ERBB/epidermal growth factor receptor family: evidence for overexpression in a subset of human mammary tumors.". Proc. Natl. Acad. Sci. U.S.A. 86 (23): 9193–7. PMID 2687875. 
  • Alimandi M, Romano A, Curia MC, et al. (1995). "Cooperative signaling of ErbB3 and ErbB2 in neoplastic transformation and human mammary carcinomas.". Oncogene 10 (9): 1813–21. PMID 7538656. 
  • Wallasch C, Weiss FU, Niederfellner G, et al. (1995). "Heregulin-dependent regulation of HER2/neu oncogenic signaling by heterodimerization with HER3.". EMBO J. 14 (17): 4267–75. PMID 7556068. 
  • Horan T, Wen J, Arakawa T, et al. (1995). "Binding of Neu differentiation factor with the extracellular domain of Her2 and Her3.". J. Biol. Chem. 270 (41): 24604–8. PMID 7592681. 
  • Shintani S, Funayama T, Yoshihama Y, et al. (1995). "Prognostic significance of ERBB3 overexpression in oral squamous cell carcinoma.". Cancer Lett. 95 (1-2): 79–83. PMID 7656248. 
  • Katoh M, Yazaki Y, Sugimura T, Terada M (1993). "c-erbB3 gene encodes secreted as well as transmembrane receptor tyrosine kinase.". Biochem. Biophys. Res. Commun. 192 (3): 1189–97. doi:10.1006/bbrc.1993.1542. PMID 7685162. 
  • Culouscou JM, Plowman GD, Carlton GW, et al. (1993). "Characterization of a breast cancer cell differentiation factor that specifically activates the HER4/p180erbB4 receptor.". J. Biol. Chem. 268 (25): 18407–10. PMID 7689552. 
  • Zelada-Hedman M, Werer G, Collins P, et al. (1995). "High expression of the EGFR in fibroadenomas compared to breast carcinomas.". Anticancer Res. 14 (5A): 1679–88. PMID 7847801. 
  • Carraway KL, Sliwkowski MX, Akita R, et al. (1994). "The erbB3 gene product is a receptor for heregulin.". J. Biol. Chem. 269 (19): 14303–6. PMID 8188716. 
  • Shintani S, Funayama T, Yoshihama Y, et al. (1996). "Expression of c-erbB family gene products in adenoid cystic carcinoma of salivary glands: an immunohistochemical study.". Anticancer Res. 15 (6B): 2623–6. PMID 8669836. 
  • Chang H, Riese DJ, Gilbert W, et al. (1997). "Ligands for ErbB-family receptors encoded by a neuregulin-like gene.". Nature 387 (6632): 509–12. doi:10.1038/387509a0. PMID 9168114. 
  • Carraway KL, Weber JL, Unger MJ, et al. (1997). "Neuregulin-2, a new ligand of ErbB3/ErbB4-receptor tyrosine kinases.". Nature 387 (6632): 512–6. doi:10.1038/387512a0. PMID 9168115. 
  • Fiddes RJ, Campbell DH, Janes PW, et al. (1998). "Analysis of Grb7 recruitment by heregulin-activated erbB receptors reveals a novel target selectivity for erbB3.". J. Biol. Chem. 273 (13): 7717–24. PMID 9516479. 
  • Jones JT, Ballinger MD, Pisacane PI, et al. (1998). "Binding interaction of the heregulinbeta egf domain with ErbB3 and ErbB4 receptors assessed by alanine scanning mutagenesis.". J. Biol. Chem. 273 (19): 11667–74. PMID 9565587. 
  • Lee H, Maihle NJ (1998). "Isolation and characterization of four alternate c-erbB3 transcripts expressed in ovarian carcinoma-derived cell lines and normal human tissues.". Oncogene 16 (25): 3243–52. doi:10.1038/sj.onc.1201866. PMID 9681822. 
  • Vijapurkar U, Cheng K, Koland JG (1998). "Mutation of a Shc binding site tyrosine residue in ErbB3/HER3 blocks heregulin-dependent activation of mitogen-activated protein kinase.". J. Biol. Chem. 273 (33): 20996–1002. PMID 9694850. 
  • Yoo JY, Hamburger AW (1999). "Interaction of the p23/p198 protein with ErbB-3.". Gene 229 (1-2): 215–21. PMID 10095121. 
  • Lin J, Adam RM, Santiestevan E, Freeman MR (1999). "The phosphatidylinositol 3'-kinase pathway is a dominant growth factor-activated cell survival pathway in LNCaP human prostate carcinoma cells.". Cancer Res. 59 (12): 2891–7. PMID 10383151.