TY - JOUR
T1 - Protective role of 17β-estradiol on medulloblastoma development in Patched1 heterozygous mice
AU - Mancuso, Mariateresa
AU - Leonardi, Simona
AU - Ceccarelli, Manuela
AU - Pasquali, Emanuela
AU - Stefano, Ilaria De
AU - Prisco, Maria Grazia
AU - Rebessi, Simonetta
AU - Tanori, Mirella
AU - Scambia, Giovanni
AU - Majo, Vincenzo Di
AU - Pazzaglia, Simonetta
AU - Saran, Anna
AU - Gallo, Daniela
PY - 2010/12/15
Y1 - 2010/12/15
N2 - Medulloblastoma (MB) is the most common pediatric tumor of the CNS, representing ∼20% of all childhood CNS tumors. Although in recent years many molecular mechanisms that control MB development have been clarified, the effects of biological factors such as sex on this tumor remain to be explained. Epidemiological data, in fact, indicate a significant difference in the incidence of MB between the 2 sexes, with considerably higher susceptibility of males than females. Besides this different susceptibility, female sex is also a significant favorable prognostic factor in MB, with girls having a much better outcome. Despite these literature data, there has been little investigation into estrogen influence on MB development. In our study, we evaluated how hormone deficiency resulting from ovariectomy and hormone replacement influences the development of early and advanced MB stages in Patched1 heterozygous mice, a well-characterized mouse model of radiation-induced MB. Susceptibility to MB development was significantly increased in ovariectomized Ptch1+/- females and restored to levels observed in control mice after estrogen replacement. We next investigated the molecular mechanisms by which estrogen might influence tumor progression and show that ERβ, but not ERα, is involved in modulation of MB development by estrogens. Finally, our study shows that a functional interaction between estrogen-and IGF-I-mediated pathways may be responsible for the effects observed.
AB - Medulloblastoma (MB) is the most common pediatric tumor of the CNS, representing ∼20% of all childhood CNS tumors. Although in recent years many molecular mechanisms that control MB development have been clarified, the effects of biological factors such as sex on this tumor remain to be explained. Epidemiological data, in fact, indicate a significant difference in the incidence of MB between the 2 sexes, with considerably higher susceptibility of males than females. Besides this different susceptibility, female sex is also a significant favorable prognostic factor in MB, with girls having a much better outcome. Despite these literature data, there has been little investigation into estrogen influence on MB development. In our study, we evaluated how hormone deficiency resulting from ovariectomy and hormone replacement influences the development of early and advanced MB stages in Patched1 heterozygous mice, a well-characterized mouse model of radiation-induced MB. Susceptibility to MB development was significantly increased in ovariectomized Ptch1+/- females and restored to levels observed in control mice after estrogen replacement. We next investigated the molecular mechanisms by which estrogen might influence tumor progression and show that ERβ, but not ERα, is involved in modulation of MB development by estrogens. Finally, our study shows that a functional interaction between estrogen-and IGF-I-mediated pathways may be responsible for the effects observed.
KW - ERα
KW - ERβ
KW - IGF-I
KW - Ptch1
KW - Radiation
UR - http://www.scopus.com/inward/record.url?scp=78249281351&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=78249281351&partnerID=8YFLogxK
U2 - 10.1002/ijc.25293
DO - 10.1002/ijc.25293
M3 - Article
C2 - 21351254
AN - SCOPUS:78249281351
SN - 0020-7136
VL - 127
SP - 2749
EP - 2757
JO - International Journal of Cancer
JF - International Journal of Cancer
IS - 12
ER -