WT1 expression distinguishes astrocytic tumor cells from normal and reactive astrocytes

被引:22
作者
Schittenhelm, Jens [1 ]
Mittelbronn, Michel [1 ]
Nguyen, Thai-Dung [1 ]
Meyermann, Richard [1 ]
Beschorner, Rudi [1 ]
机构
[1] Univ Tubingen Hosp, Inst Brain Res, Tubingen, Germany
关键词
astrocytoma; astrogliosis; neoplastic astrocytes; normal brain; WT1;
D O I
10.1111/j.1750-3639.2008.00127.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Particularly in small brain biopsies, it might be difficult to distinguish reactive astrogliosis from low-grade or infiltration zones of high-grade astrocytomas. So far no immunohistochemical marker allows a reliable distinction. Recently, the over-expression of Wilms' tumor gene product WT1 was reported in astrocytic tumor cells. However, no sufficient data on WT1 expression in normal or reactive astrocytes are available. Therefore, we investigated WT1 expression in paraffin-embedded brain sections from 28 controls, 48 cases with astrogliosis of various etiology and 219 astrocytomas [World Health Organization (WHO) grades I-IV] by immunohistochemistry. In normal brains and in astrogliosis, expression of WT1 was restricted to endothelial cells. In astrocytomas, WT1-positive tumor cells were found in pilocytic astrocytomas (66.7% of cases), diffuse astrocytomas (52.7%) WHO grade II (52.7%), anaplastic astrocytomas (83.4%) and glioblastomas (98.1%). Overall, the majority of all astrocytic neoplasms (84.5%) expressed WT1. Establishing a cut-off value of 0% immunoreactive tumor cells served to recognize neoplastic astrocytes with 100% specificity and 68% sensitivity and was associated with positive and negative predictive values of 1 and 0.68, respectively. Therefore, WT1 expression in astrocytes indicates a neoplastic origin and might represent an important diagnostic tool to differentiate reactive from neoplastic astrocytes by immunohistochemistry.
引用
收藏
页码:344 / 353
页数:10
相关论文
共 62 条
[1]  
Agapova OA, 2001, GLIA, V33, P205, DOI 10.1002/1098-1136(200103)33:3<205::AID-GLIA1019>3.0.CO
[2]  
2-D
[3]   Immunohistochemical detection of EGFRvIII in high malignancy grade astrocytomas and evaluation of prognostic significance [J].
Aldape, KD ;
Ballman, K ;
Furth, A ;
Buckner, JC ;
Giannini, C ;
Burger, PC ;
Scheithauer, BW ;
Jenkins, RB ;
James, CD .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2004, 63 (07) :700-707
[4]   THE EXPRESSION OF THE WILMS-TUMOR GENE, WT1, IN THE DEVELOPING MAMMALIAN EMBRYO [J].
ARMSTRONG, JF ;
PRITCHARDJONES, K ;
BICKMORE, WA ;
HASTIE, ND ;
BARD, JBL .
MECHANISMS OF DEVELOPMENT, 1993, 40 (1-2) :85-97
[5]   Expression and role of cadherins in astrocytic tumors. [J].
Asano K. ;
Kubo O. ;
Tajika Y. ;
Huang M.C. ;
Takakura K. ;
Ebina K. ;
Suzuki S. .
Brain Tumor Pathology, 1997, 14 (1) :27-33
[6]  
Aschner M, 2002, BRAIN PATHOL, V12, P475
[7]   Identification of a highly immunogenic HLA-A*01-binding T cell epitope of WT1 [J].
Asemissen, Anne Marie ;
Keilholz, Ulrich ;
Tenzer, Stefan ;
Mueller, Margret ;
Walter, Steffen ;
Stevanovic, Stefan ;
Schild, Hansjoerg ;
Letsch, Anne ;
Thiel, Eckhard ;
Rammensee, Hans-Georg ;
Scheibenbogen, Carmen .
CLINICAL CANCER RESEARCH, 2006, 12 (24) :7476-7482
[8]   Predominant expression of mutant EGFR (EGFRvIII) is rare in primary glioblastomas [J].
Biernat, W ;
Huang, H ;
Yokoo, H ;
Kleihues, P ;
Ohgaki, H .
BRAIN PATHOLOGY, 2004, 14 (02) :131-136
[9]   ISOLATION, CHARACTERIZATION, AND EXPRESSION OF THE MURINE WILMS-TUMOR GENE (WT1) DURING KIDNEY DEVELOPMENT [J].
BUCKLER, AJ ;
PELLETIER, J ;
HABER, DA ;
GLASER, T ;
HOUSMAN, DE .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (03) :1707-1712
[10]  
BURGER PC, 2002, SURG PATHOLOGY NERVO, P160