Karamitopoulou E, Perentes E, Diamantis I
Sandoz Pharma Ltd., Department of Toxicology, Basel, Switzerland.
Acta Neuropathol. 1993;85(6):611-6. doi: 10.1007/BF00334670.
Formalin-fixed, paraffin-embedded surgical specimens from 137 primary central nervous system tumors, including 26 astrocytomas (21 fibrillary, 1 protoplasmic, 1 gemistocytic and 3 pilocytic), 26 anaplastic astrocytomas, 9 glioblastomas, 1 gliosarcoma, 8 oligodendrogliomas, 4 ependymomas, 1 anaplastic ependymoma, 2 subependymomas, 3 paragangliomas, and 57 meningiomas, were immunostained with the CM1 polyclonal (pAb) and the DO-7 monoclonal (mAb) antibodies against the p53 protein, using the streptavidin/peroxidase method. In addition, two series of 17 and 9 medulloblastomas were also immunostained with the above pAb and mAb, respectively. p53 protein expression was observed in 7 fibrillary astrocytomas, 17 anaplastic astrocytomas, 5 glioblastomas, 1 gliosarcoma, 1 oligodendroglioma, 1 anaplastic ependymoma, and 4 meningiomas with the CM1 pAb. An additional 10 cases (i.e., 3 anaplastic astrocytomas and 7 meningiomas) were found to be p53 protein positive with the DO-7 mAb. Of the medulloblastomas, 8 (of the 17) and 4 (of the 9) were found to express p53 protein with CM1 pAb and DO-7 mAb, respectively. Our results indicate that p53 protein is expressed in a number of central nervous system neoplasms, and suggest that in astrocytic tumors a possible association may exist between p53 protein expression and tumor progression through increasing histological grades of malignancy.
采用链霉抗生物素蛋白/过氧化物酶法,用抗p53蛋白的CM1多克隆抗体(pAb)和DO-7单克隆抗体(mAb)对137例原发性中枢神经系统肿瘤的福尔马林固定、石蜡包埋手术标本进行免疫染色,这些肿瘤包括26例星形细胞瘤(21例纤维型、1例原浆型、1例肥胖型和3例毛细胞型)、26例间变性星形细胞瘤、9例胶质母细胞瘤、1例胶质肉瘤、8例少突胶质细胞瘤、4例室管膜瘤、1例间变性室管膜瘤、2例室管膜下瘤、3例副神经节瘤和57例脑膜瘤。此外,两组分别为17例和9例的髓母细胞瘤也分别用上述pAb和mAb进行免疫染色。用CM1 pAb在7例纤维型星形细胞瘤、17例间变性星形细胞瘤、5例胶质母细胞瘤、1例胶质肉瘤、1例少突胶质细胞瘤、1例间变性室管膜瘤和4例脑膜瘤中观察到p53蛋白表达。另外10例(即3例间变性星形细胞瘤和7例脑膜瘤)用DO-7 mAb检测为p53蛋白阳性。在髓母细胞瘤中,分别有8例(17例中的)和4例(9例中的)用CM1 pAb和DO-7 mAb检测到表达p53蛋白。我们的结果表明p53蛋白在多种中枢神经系统肿瘤中表达,并提示在星形细胞肿瘤中,p53蛋白表达与肿瘤通过增加恶性组织学分级而进展之间可能存在关联。