TY - JOUR
T1 - Prognostic significance of the immunohistochemical index of survivin in glioma
T2 - A comparative study with the MIB-1 index
AU - Uematsu, Masaki
AU - Ohsawa, Ikuroh
AU - Aokage, Toshiyuki
AU - Nishimaki, Kiyomi
AU - Matsumoto, Kouji
AU - Takahashi, Hiroshi
AU - Asoh, Sadamitsu
AU - Teramoto, Akira
AU - Ohta, Shigeo
PY - 2005/5
Y1 - 2005/5
N2 - Objective: Survivin has been identified as a protein expressed in cancer cells and a member of the inhibitor-of-apoptosis protein family. Recent studies suggest that the expression of survivin increases during the G2/M phase of the cell cycle, and may be used in clinical prognosis. We examined whether survivin expression in human gliomas would be a correlative of prognosis. Methods: We prepared polyclonal anti-survivin serum to establish a survivin index for stained sections, using an immunohistochemical procedure, according to the method used for scoring MIB-1 index, and then stained 29 paraffin-embedded sections from surgical specimens of 29 patients who were classified into three grades of World Health Organization with the mean age of low grade astocytoma (grade II) being 34.7; anaplastic astrocytoma (grade III), 48.8; and glioblastoma multiform (grade IV), 58.4. Results: On staining with the anti-survivin antiserum, all specimens contained positive cells, but the survivin index was heterogeneous among grades. The mean percentage of immunoreactive cells in each specimen was 70.0 (SD 18.2) in grade II, 81.3 (16.5) in grade III, and 85.0 (13.6) in grade IV. Then we compared the survivin index to the MIB-1 index and found that in low-grade gliomas (grade II and III), the difference in survival times between the high and low survivin indexes was significant (P = 0.007), whereas that between the high and low MIB-1 indexes was not significant (P = 0.092). Conclusion: Survivin is more sensitive marker than MIB-1 for the evaluation of low-grade gliomas in that it helps to predict patient survival. Much larger glioma patient series are needed to validate the findings of our limited study.
AB - Objective: Survivin has been identified as a protein expressed in cancer cells and a member of the inhibitor-of-apoptosis protein family. Recent studies suggest that the expression of survivin increases during the G2/M phase of the cell cycle, and may be used in clinical prognosis. We examined whether survivin expression in human gliomas would be a correlative of prognosis. Methods: We prepared polyclonal anti-survivin serum to establish a survivin index for stained sections, using an immunohistochemical procedure, according to the method used for scoring MIB-1 index, and then stained 29 paraffin-embedded sections from surgical specimens of 29 patients who were classified into three grades of World Health Organization with the mean age of low grade astocytoma (grade II) being 34.7; anaplastic astrocytoma (grade III), 48.8; and glioblastoma multiform (grade IV), 58.4. Results: On staining with the anti-survivin antiserum, all specimens contained positive cells, but the survivin index was heterogeneous among grades. The mean percentage of immunoreactive cells in each specimen was 70.0 (SD 18.2) in grade II, 81.3 (16.5) in grade III, and 85.0 (13.6) in grade IV. Then we compared the survivin index to the MIB-1 index and found that in low-grade gliomas (grade II and III), the difference in survival times between the high and low survivin indexes was significant (P = 0.007), whereas that between the high and low MIB-1 indexes was not significant (P = 0.092). Conclusion: Survivin is more sensitive marker than MIB-1 for the evaluation of low-grade gliomas in that it helps to predict patient survival. Much larger glioma patient series are needed to validate the findings of our limited study.
KW - Glioma
KW - MIB-1 index
KW - Prognosis
KW - Survivin
KW - Tumor marker
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U2 - 10.1007/s11060-004-2353-3
DO - 10.1007/s11060-004-2353-3
M3 - Article
C2 - 15937645
AN - SCOPUS:20944436621
SN - 0167-594X
VL - 72
SP - 231
EP - 238
JO - Journal of neuro-oncology
JF - Journal of neuro-oncology
IS - 3
ER -