| Literature DB >> 28377225 |
Sen Zhang1, Jishun Lu2, Zhijue Xu3, Xia Zou4, Xue Sun5, Yingjiao Xu3, Aidong Shan3, Jiaoyang Lu1, Xialin Yan1, Yalu Cui3, Wei Yan3, Yuguo Du5, Jianguo Gu6, Minhua Zheng1, Bo Feng7, Yan Zhang8.
Abstract
Elevated expression of β-galactoside α2,6-sialyltranferase 1 (ST6GAL1) has been observed in colorectal cancer (CRC) and demonstrated to be important for its tumorigenesis. Here, we found that ST6GAL1 expression was significantly higher in non-metastatic tumors (stage I and II) than that in metastatic tumors (stage III and IV) using 62 pair-matched tumor/normal tissues. To elucidate the molecular mechanisms of how ST6GAL1 affected the CRC progression, we performed a global identification of the substrates of ST6GAL1 in the colon adenocarcinoma cell line SW480. A total of 318 membrane proteins were identified differentially affected by ST6GAL1 overexpression using metabolic labeling and proteomic analysis. Subsequent bioinformatic analysis revealed a list of potential substrates that might mediate the different functions of ST6GAL1 in CRC including cell movement, cell death and survival. Taken together, these results indicate a dynamic change in the expression of ST6GAL1 during the CRC progression and provide a list of sialylated proteins potentially relevant to the different functions of ST6GAL1 in CRC.Entities:
Keywords: Colorectal cancer; Metabolic labeling; ST6GAL1; Sialylation
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Year: 2017 PMID: 28377225 DOI: 10.1016/j.bbrc.2017.03.167
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575