肿瘤进展
结直肠癌
癌变
生物
癌症
转移
癌症研究
腺癌
病理
医学
遗传学
作者
Sen Zhang,Jishun Lu,Zhijue Xu,Xia Zou,Xue Sun,Yingjiao Xu,Aidong Shan,Jiao Lu,Xialin Yan,Yalu Cui,Wei Yan,Yuguo Du,Jianguo Gu,Minhua Zheng,Bo Feng,Yan Zhang
标识
DOI:10.1016/j.bbrc.2017.03.167
摘要
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.
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