| Literature DB >> 26124270 |
Kai Song1, Brett H Herzog2, Jianxin Fu3, Minjia Sheng4, Kirk Bergstrom1, J Michael McDaniel1, Yuji Kondo1, Samuel McGee1, Xiaofeng Cai1, Ping Li5, Hong Chen6, Lijun Xia7.
Abstract
Mucin-type core 1-derived O-glycans, one of the major types of O-glycans, are highly expressed in mammary gland epithelium. Abnormal O-glycans such as Tn antigen are found in over 90% of breast cancers; however, the in vivo role of these aberrant O-glycans in the etiology of breast cancer is unclear. We generated mice with mammary epithelial specific deletion of core 1-derived O-glycans. By crossing with two spontaneous mouse breast cancer models, we determined that loss of core 1-derived O-glycans delays the onset and progression of breast cancer development. Deficiency of core 1 O-glycosylation impaired the localization of Muc1, a major O-glycoprotein, on the apical surfaces of mammary epithelium. Signaling mediated by Muc1, which is critical for breast cancer development, was also defective in the absence of core 1 O-glycans. This study reveals an unexpected role of core 1-derived O-glycans in breast cancer development in mice.Entities:
Keywords: breast cancer; cell proliferation; glycosylation; mouse; mucin 1, cell surface associated (MUC1); tumor microenvironment
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Year: 2015 PMID: 26124270 PMCID: PMC4536426 DOI: 10.1074/jbc.M115.654483
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157