Promoter hypermethylation correlates with the HSulf-1 silencing in human breast and gastric cancer

被引:39
作者
Chen, Zhao [1 ]
Fan, Jie-Qing [1 ]
Li, Jie [1 ]
Li, Qiu-Shi [1 ]
Yan, Zhao [2 ]
Jia, Xue-Ke [3 ]
Liu, Wei-Dong [4 ]
Wei, Li-Jun [5 ]
Zhang, Feng-Zhi [9 ]
Gao, Hong [6 ]
Xu, Jun-Pu [7 ]
Dong, Xiao-Ming [7 ]
Dai, Jie [7 ]
Zhou, Hai-Meng [1 ,8 ]
机构
[1] Tsinghua Univ, Dept Biol Sci & Biotechnol, Beijing 100084, Peoples R China
[2] Tianjin Med Univ, Key Lab Breast Canc Prevent & Therapy, Minist Educ China, Canc Inst & Hosp, Tianjin, Peoples R China
[3] Hengxing Hosp, Dept Oncol, Baoding, Hebei, Peoples R China
[4] Tangshan Peoples Hosp, Tangshan, Hebei, Peoples R China
[5] Shanxi Tumor Hosp, Dept Gynecol 1, Taiyuan, Shanxi, Peoples R China
[6] Qinghai Gen Hosp, Xining, Qinghai, Peoples R China
[7] Beijing ACCB Biotech Ltd, Beijing, Peoples R China
[8] Tsinghua Univ, Yangtze Delta Reg Inst, Jiaxing, Zhejiang, Peoples R China
[9] Chengde N Hosp, Chengde, Hebei, Peoples R China
关键词
HSulf-1; promoter; hypermethylation; cancer; HEPARAN-SULFATE PROTEOGLYCANS; CELL-SURFACE; IN-VIVO; TUMOR; WNT; MECHANISMS; CARCINOMA; SERUM; PCR;
D O I
10.1002/ijc.23960
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The HSulf-1 gene is an important factor that modulates the sulfation status of heparan sulfate proteoglycans (HSPGs) in the extracellular matrix, resulting in disturbance of HSPG-related signal transduction pathways. Recently, HSulf-1 has been reported to be down-regulated in several human cancers. In this study, we first cloned and characterized the 5' promoter region of the HSul-1 gene (around 400 bp) that contained high basal promoter activity. We also found that this functional promoter region was hypermethylated in a number of human cancer cell lines. Furthermore, we found that hypermethylation in this promoter region correlated with the down-regulation of the HSulf-1 expression in human breast and gastric cancer cell lines and tissue samples. These results suggest that the promoter hypermethylation may be one of the mechanisms of the HSulf-1 gene silencing in human breast and gastric cancers. Finally, we demonstrated that the HSulf-1 promoter was more frequently (p < 0.05) methylated in cell-free DNA extracted from serum samples of human breast and gastric cancer patients than that of healthy people (76.2%, 55.0% and 19.0%, respectively), indicating that detection of the HSulf-1 promoter methylation in serum samples may have clinical implications in early detection and diagnosis of human breast and gastric cancers. (C) 2008 Wiley-Liss, Inc.
引用
收藏
页码:739 / 744
页数:6
相关论文
共 21 条
[11]   Loss of HSulf-1 up-regulates heparin-binding growth factor signaling in cancer [J].
Lai, JP ;
Chien, J ;
Staub, J ;
Avula, R ;
Greene, EL ;
Matthews, TA ;
Smith, DI ;
Kaufmann, SH ;
Roberts, LR ;
Shridhar, V .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (25) :23107-23117
[12]  
Lee TL, 2002, CLIN CANCER RES, V8, P1761
[13]   Enhanced levels of Hsulf-1 interfere with heparin-binding growth factor signaling in pancreatic cancer [J].
Li, Junsheng ;
Kleeff, Joerg ;
Abiatari, Ivane ;
Kayed, Hany ;
Giese, Nathalia A. ;
Felix, Klaus ;
Giese, Thomas ;
Buchler, Markus W. ;
Friess, Helmut .
MOLECULAR CANCER, 2005, 4 (1)
[14]   Functions of heparan sulfate proteoglycans in cell signaling during development [J].
Lin, XH .
DEVELOPMENT, 2004, 131 (24) :6009-6021
[15]   Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCT method [J].
Livak, KJ ;
Schmittgen, TD .
METHODS, 2001, 25 (04) :402-408
[16]   Cloning and characterization of two extracellular heparin-degrading endosulfatases in mice and humans [J].
Morimoto-Tomita, M ;
Uchimura, K ;
Werb, Z ;
Hemmerich, S ;
Rosen, SD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (51) :49175-49185
[17]   HSulf-1 inhibits angiogenesis and tumorigenesis in vivo [J].
Narita, Keishi ;
Staub, Julie ;
Chien, Jeremy ;
Meyer, Kristy ;
Bauer, Maret ;
Friedl, Andreas ;
Ramakrishnan, Sundaram ;
Shridhar, Viji .
CANCER RESEARCH, 2006, 66 (12) :6025-6032
[18]   Extracellular Sulfatases, Elements of the Wnt Signaling Pathway, Positively Regulate Growth and Tumorigenicity of Human Pancreatic Cancer Cells [J].
Nawroth, Roman ;
van Zante, Annemieke ;
Cervantes, Sara ;
McManus, Michael ;
Hebrok, Matthias ;
Rosen, Steven D. .
PLOS ONE, 2007, 2 (04)
[19]   Wnts and Hedgehogs: lipid-modified proteins and similarities in signaling mechanisms at the cell surface [J].
Nusse, R .
DEVELOPMENT, 2003, 130 (22) :5297-5305
[20]   Cell surface heparan sulfate proteoglycans: Selective regulators of ligand-receptor encounters [J].
Park, PW ;
Reizes, O ;
Bernfield, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (39) :29923-29926