TY - JOUR
T1 - Immunohistochemical analysis of SOX6 expression in human brain tumors
AU - Ueda, Ryo
AU - Yoshida, Kazunari
AU - Kawakami, Yutaka
AU - Kawase, Takeshi
AU - Toda, Masahiro
PY - 2004/12/1
Y1 - 2004/12/1
N2 - We previously demonstrated that the developmentally regulated gene, SOX6, is strongly expressed in glioma cells and in the fetal brain, but only faintly in the normal adult brain. Recent studies have indicated that brain tumor cells may share antigens, signaling systems, and behavior with neural stem/progenitor cells. To test the validity of this proposition, we analyzed the expression of SOX6 in various human central nervous system (CNS) tumors. Immunohistochemical analysis revealed that astrocytic and oligodendroglial tumors expressed SOX6; neuronal-glial cell tumors (central neurocytoma) and embryonal tumors (medulloblastoma), which arise from multipotential stem cell precursors, also showed a high intensity of SOX6 staining. In contrast, ependymal tumors (ependymoma and subependymoma), meningioma, and schwannoma, which are all well differentiated tumors, showed either no staining or only faint staining for SOX6. These results suggest that SOX6 may be expressed in bipotential or multipotential cells capable of neuronal and glial differentiation, but not in fully differentiated cells. SOX6 may be a useful marker for the diagnosis of tumors arising from immature bipotential cells that may differentiate into neuronal and glial cells.
AB - We previously demonstrated that the developmentally regulated gene, SOX6, is strongly expressed in glioma cells and in the fetal brain, but only faintly in the normal adult brain. Recent studies have indicated that brain tumor cells may share antigens, signaling systems, and behavior with neural stem/progenitor cells. To test the validity of this proposition, we analyzed the expression of SOX6 in various human central nervous system (CNS) tumors. Immunohistochemical analysis revealed that astrocytic and oligodendroglial tumors expressed SOX6; neuronal-glial cell tumors (central neurocytoma) and embryonal tumors (medulloblastoma), which arise from multipotential stem cell precursors, also showed a high intensity of SOX6 staining. In contrast, ependymal tumors (ependymoma and subependymoma), meningioma, and schwannoma, which are all well differentiated tumors, showed either no staining or only faint staining for SOX6. These results suggest that SOX6 may be expressed in bipotential or multipotential cells capable of neuronal and glial differentiation, but not in fully differentiated cells. SOX6 may be a useful marker for the diagnosis of tumors arising from immature bipotential cells that may differentiate into neuronal and glial cells.
KW - Brain tumor
KW - Neural stem/progenitor cell
KW - SOX6
KW - Undifferentiated cell
UR - http://www.scopus.com/inward/record.url?scp=13244249772&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=13244249772&partnerID=8YFLogxK
U2 - 10.1007/BF02482186
DO - 10.1007/BF02482186
M3 - Article
C2 - 15696972
AN - SCOPUS:13244249772
SN - 1433-7398
VL - 21
SP - 117
EP - 120
JO - Brain tumor pathology
JF - Brain tumor pathology
IS - 3
ER -