TY - JOUR
T1 - Human hedgehog interacting protein expression and promoter methylation in medulloblastoma cell lines and primary tumor samples
AU - Shahi, Mehdi H.
AU - Afzal, Mohammad
AU - Sinha, Subrata
AU - Eberhart, Charles G.
AU - Rey, Juan A.
AU - Fan, Xing
AU - Castresana, Javier S.
N1 - Funding Information:
Acknowledgments M.H. Shahi was a fellow of Agencia Española de Cooperación Internacional, Madrid, Spain. J.S. Castresana expresses his gratitude to the Asociación Española de Pediatría, for the VIII Premio Nutribén de Investigación Pediátrica; the Sociedad Española de Hematología y Oncología Pediátricas; and the Fundación Mapfre Medicina, Madrid. This research was supported in part by grants from the Departmento de Salud del Gobierno de Navarra (9/07), Caja Navarra (08/13912), and Fundación Universitaria de Navarra, Pamplona; and Fondo de Investigación Sanitaria (PI081849), Madrid, Spain.
PY - 2011/6
Y1 - 2011/6
N2 - 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.
AB - 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.
KW - GLI1
KW - Human hedgehog interacting protein (HHIP)
KW - Medulloblastoma
KW - Melting curve analysis-methylation (MCA-Meth)
KW - Methylation
UR - http://www.scopus.com/inward/record.url?scp=79959814946&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=79959814946&partnerID=8YFLogxK
U2 - 10.1007/s11060-010-0401-8
DO - 10.1007/s11060-010-0401-8
M3 - Article
C2 - 20853133
AN - SCOPUS:79959814946
SN - 0167-594X
VL - 103
SP - 287
EP - 296
JO - Journal of neuro-oncology
JF - Journal of neuro-oncology
IS - 2
ER -