Evidence that MIG-6 is a tumor-suppressor gene
- PMID: 16819504
- DOI: 10.1038/sj.onc.1209790
Evidence that MIG-6 is a tumor-suppressor gene
Abstract
Mitogen-inducible gene 6 (MIG-6) is located in human chromosome 1p36, a locus frequently associated with human lung cancer. MIG-6 is a negative regulator of epidermal growth factor (EGF) signaling, and we show that Mig-6 - like EGF - is induced by hepatocyte growth factor/scatter factor (HGF/SF) in human lung cancer cell lines. Frequently, the receptors for both factors, EGFR and Met, are expressed in same lung cancer cell line, and MIG-6 is induced by both factors in a mitogen-activated protein kinase-dependent fashion. However, not all tumor lines express MIG-6 in response to either EGF or HGF/SF. In these cases, we find missense and nonsense mutations in the MIG-6 coding region, as well as evidence for MIG-6 transcriptional silencing. Moreover, germline disruption of Mig-6 in mice leads to the development of animals with epithelial hyperplasia, adenoma, and adenocarcinoma in organs like the lung, gallbladder, and bile duct. These data suggests that MIG-6 is a tumor-suppressor gene and is therefore a candidate gene for the frequent 1p36 genetic alterations found in lung cancer.
Similar articles
-
Mitogen-inducible gene-6 is a multifunctional adaptor protein with tumor suppressor-like activity in papillary thyroid cancer.J Clin Endocrinol Metab. 2011 Mar;96(3):E554-65. doi: 10.1210/jc.2010-1800. Epub 2010 Dec 29. J Clin Endocrinol Metab. 2011. PMID: 21190978
-
Mitogen-inducible gene-6 is a negative regulator of epidermal growth factor receptor signaling in hepatocytes and human hepatocellular carcinoma.Hepatology. 2010 Apr;51(4):1383-90. doi: 10.1002/hep.23428. Hepatology. 2010. PMID: 20044804
-
Low expression of Mig-6 is associated with poor survival outcome in NSCLC and inhibits cell apoptosis via ERK-mediated upregulation of Bcl-2.Oncol Rep. 2014 Apr;31(4):1707-14. doi: 10.3892/or.2014.3050. Epub 2014 Feb 24. Oncol Rep. 2014. PMID: 24573418
-
Mig-6, signal transduction, stress response and cancer.Cell Cycle. 2007 Mar 1;6(5):507-13. doi: 10.4161/cc.6.5.3928. Epub 2007 Mar 31. Cell Cycle. 2007. PMID: 17351343 Review.
-
Feedback inhibitors of the epidermal growth factor receptor signaling pathways.Int J Biochem Cell Biol. 2009 Mar;41(3):511-5. doi: 10.1016/j.biocel.2008.06.019. Epub 2008 Aug 9. Int J Biochem Cell Biol. 2009. PMID: 18762271 Review.
Cited by
-
Mig-6 regulates endometrial genes involved in cell cycle and progesterone signaling.Biochem Biophys Res Commun. 2015 Jul 10;462(4):409-14. doi: 10.1016/j.bbrc.2015.04.146. Epub 2015 May 12. Biochem Biophys Res Commun. 2015. PMID: 25976672 Free PMC article.
-
The antitumorigenic function of EGFR in metastatic breast cancer is regulated by expression of Mig6.Neoplasia. 2015 Jan;17(1):124-33. doi: 10.1016/j.neo.2014.11.009. Neoplasia. 2015. PMID: 25622905 Free PMC article.
-
ERBB receptor feedback inhibitor 1 regulation of estrogen receptor activity is critical for uterine implantation in mice.Biol Reprod. 2010 Apr;82(4):706-13. doi: 10.1095/biolreprod.109.081307. Epub 2009 Dec 16. Biol Reprod. 2010. PMID: 20018910 Free PMC article.
-
Gene 33/Mig6/ERRFI1, an Adapter Protein with Complex Functions in Cell Biology and Human Diseases.Cells. 2021 Jun 22;10(7):1574. doi: 10.3390/cells10071574. Cells. 2021. PMID: 34206547 Free PMC article. Review.
-
Nuclear Gene 33/Mig6 regulates the DNA damage response through an ATM serine/threonine kinase-dependent mechanism.J Biol Chem. 2017 Oct 6;292(40):16746-16759. doi: 10.1074/jbc.M117.803338. Epub 2017 Aug 25. J Biol Chem. 2017. PMID: 28842482 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Molecular Biology Databases
Research Materials
Miscellaneous