O-GlcNAcylation is a novel regulator of lung and colon cancer malignancy

被引:230
作者
Mi, Wenyi [1 ]
Gu, Yuchao [1 ]
Han, Cuifang [1 ]
Liu, Haiyan [1 ]
Fan, Qiong [1 ]
Zhang, Xinling [1 ]
Cong, Qi [1 ]
Yu, Wengong [1 ]
机构
[1] Ocean Univ China, Key Lab Marine Drugs, Chinese Minist Educ, Sch Med & Pharm,Key Lab Glycosci & Glycotech Shan, Qingdao 266003, Peoples R China
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 2011年 / 1812卷 / 04期
关键词
O-GlcNAc; Lung cancer; Colon cancer; Immunohistochemistry; MAMMALIAN-CELLS; GENE-EXPRESSION; BREAST-CANCER; X-CHROMOSOME; STRESS; PHOSPHORYLATION; ADENOCARCINOMA; METASTASIS; METABOLISM; VIABILITY;
D O I
10.1016/j.bbadis.2011.01.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
O-GlcNAc is a monosaccharide attached to serine or threonine hydroxyl moieties on numerous nuclear and cytoplasmic proteins; O-GlcNAcylation is dynamically regulated by O-GlcNAc transferase (OGT) and O-GlcNAcase (OGA). Although recent studies have shown that O-GlcNAcylation plays essential roles in breast cancer progression, it is also necessary to know whether O-GlcNAcylation is involved in other types of human cancer. In this study, O-GlcNAcylation levels and the expressions of OCT and OGA in human lung and colon cancer tissues were examined by immunohistochemistry analysis. We found that O-GlcNAcylation as well as OCT expression was significantly elevated in the cancer tissues compared with that in the corresponding adjacent tissues. Additionally, the roles of O-GlcNAcylation in the malignancy of lung and colon cancer were investigated in vitro. The results showed that O-GlcNAcylation markedly enhanced the anchorage-independent growth of lung and colon cancer cells; O-GlcNAcylation could also enhance lung and colon cancer invasion in a context-dependent manner. All together, this study suggests that O-GlcNAcylation might play important roles in lung and colon cancer formation and progression, and may be a valuable target for diagnosis and therapy of cancer. Crown Copyright (C) 2011 Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:514 / 519
页数:6
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