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Varisli, Lokman; Ozturk, Bilge E.; Akyuz, Gencer K.; Korkmaz, Kemal S.
{ "DOI": "10.1002/jcb.24956", "abstract": "Previously, it has been reported that HN1 is involved in cytoplasmic retention and degradation of androgen receptor in an AKT dependent manner. As HN1 is a hormone inducible gene, and has been shown that it is upregulated in various cancers, we studied the importance of HN1 function in -catenin signaling in prostate cancer cell line, PC-3 and mammary cancer cell line MDA-MB231. Here, we demonstrated that HN1 physically associates with GSK3/-catenin destruction complex and abundantly localizes to cytoplasm, especially when the GSK3 is phosphorylated on S9 residue. Further, ectopic HN1 expression results an increase in the -catenin degradation leading to loss of E-cadherin interaction, concurrently contributing to actin re-organization, colony formation and migration in cancer cell lines. Thus, we report that HN1 is an essential factor for -catenin turnover and signaling, augments cell growth and migration in prostate cancer cells. J. Cell. Biochem. 116: 170-178, 2015. (c) 2014 Wiley Periodicals, Inc.", "author": [ { "family": "Varisli", "given": " Lokman" }, { "family": "Ozturk", "given": " Bilge E." }, { "family": "Akyuz", "given": " Gencer K." }, { "family": "Korkmaz", "given": " Kemal S." } ], "container_title": "JOURNAL OF CELLULAR BIOCHEMISTRY", "id": "80041", "issue": "1", "issued": { "date-parts": [ [ 2015, 1, 1 ] ] }, "page": "170-178", "title": "HN1 Negatively Influences the beta-Catenin/E-Cadherin Interaction, and Contributes to Migration in Prostate Cells", "type": "article-journal", "volume": "116" }
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