c-erbB-2 protein expression in astrocytic tumors of the brain

被引:4
作者
Reszec, Joanna [1 ]
Bernaczyk, Piotr S. [1 ]
Milewski, Robert [3 ]
Chyczewski, Lech [1 ]
Mariak, Zenon [2 ]
机构
[1] Med Univ Bialystok, Dept Med Pathomorphol, PL-15269 Bialystok, Poland
[2] Med Univ Bialystok, Dept Neurosurg, PL-15269 Bialystok, Poland
[3] Med Univ Bialystok, Dept Stat & Med Informat, PL-15269 Bialystok, Poland
来源
MEDICAL SCIENCE MONITOR | 2011年 / 17卷 / 08期
关键词
astrocytoma; glioblastoma; immunohistochemistry; c-erbB-2; GLIOBLASTOMA-MULTIFORME; GLIOMA; CELLS; IMMUNOHISTOCHEMISTRY; OVEREXPRESSION; RADIOTHERAPY; RECEPTORS; ABSENCE; GROWTH;
D O I
10.12659/MSM.881900
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Astrocytic tumors are the primary brain tumors, which often progress to glioblastoma, a highly malignant neoplasm of the central nervous system. There is much new data regarding to the formation and progression of these tumors; however, glioblastoma remains one of the most fatal neoplasms in humans. The aim of the study was to evaluate the role of c-erbB-2 protein expression in various groups of astrocytic tumors. Material/Methods: 65 cases of astrocytic tumors were divided into 3 groups: diffuse astrocytoma (group I; n=17 cases), anaplastic astrocytoma (group II; n=23 cases) and glioblastoma (group III; n=25 cases). C-erbB-2 protein expression was estimated semiquantitatively on immunohistochemically stained tissue sections using antibodies against c-erbB-2 protein. Statistical analysis was performed in all examined groups. Results: The c-erbB-2 protein expression was observed in 15 out of 17 cases (88.3%) in group I, 22 out of 25 cases (88%) cases in group II, and in 19 out of 23 cases (82.6%) in group III. There were no statistically significant differences between the examined groups. The strongest c-erbB-2 immunoexpression was observed in low grade astrocytomas (diffuse astrocytomas G2); in the glioblastoma group the c-erbB-2 protein expression was weak and 17.4% of cases were negative. Conclusions: C-erbB-2 protooncogene alteration is an early phenomenon in glial tumor development and progression.
引用
收藏
页码:BR216 / BR220
页数:5
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