Human hedgehog interacting protein expression and promoter methylation in medulloblastoma cell lines and primary tumor samples

被引:24
|
作者
Shahi, Mehdi H. [1 ,2 ,3 ]
Afzal, Mohammad [2 ]
Sinha, Subrata [3 ]
Eberhart, Charles G. [4 ]
Rey, Juan A. [5 ]
Fan, Xing [6 ]
Castresana, Javier S. [1 ]
机构
[1] Univ Navarra, Sch Sci, Brain Tumor Biol Unit CIFA, Pamplona 31008, Spain
[2] Aligarh Muslim Univ, Dept Zool, Aligarh 202002, Uttar Pradesh, India
[3] All India Inst Med Sci, Dept Biochem, New Delhi 110029, India
[4] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21205 USA
[5] La Paz Univ Hosp, Res Unit, Madrid, Spain
[6] Univ Michigan, Sch Med, Dept Neurosurg, Ann Arbor, MI USA
关键词
Human hedgehog interacting protein (HHIP); Medulloblastoma; Methylation; Melting curve analysis-methylation (MCA-Meth); GLI1; BINDING PROTEIN; HUMAN HOMOLOG; CARCINOMA; GENE; PATHWAY; GROWTH; CANCER; DROSOPHILA; MUTATIONS; HEAD;
D O I
10.1007/s11060-010-0401-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Medulloblastoma is the most common pediatric brain tumor and its development is affected by genetic and epigenetic factors. In this study we found there is low or no expression of the hedgehog interacting protein (HHIP), a negative regulator of the sonic hedgehog pathway, in most medulloblastoma cell lines and primary samples explored. We proceeded to promoter methylation assays of this gene by MCA-Meth, and found that HHIP was hypermethylated in all medulloblastoma cell lines, but only in 2 out of 14 (14%) primary tumor samples. Methylation correlated with low or unexpressed HHIP in cell lines but not in primary tumor samples. These results suggest the possibility of epigenetic regulation of HHIP in medulloblastoma, similarly to gastric, hepatic and pancreatic cancer. However, HHIP seems to be not only under regulation of promoter methylation, but under other factors involved in the control of its low levels of expression in medulloblastoma.
引用
收藏
页码:287 / 296
页数:10
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