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蛋白质基因产物(PGP)9.5在诊断性(神经)肿瘤学中的应用。一项免疫形态学研究。

Protein gene product (PGP) 9.5 in diagnostic (neuro-) oncology. An immunomorphological study.

作者信息

Ermisch B, Schwechheimer K

机构信息

Department of Neuropathology, University of Freiburg im Breisgau, Germany.

出版信息

Clin Neuropathol. 1995 May-Jun;14(3):130-6.

PMID:7671453
Abstract

Most likely identical to ubiquitin carboxyl-terminal hydrolase isozyme L1 (UCH-L1), protein gene product (PGP) 9.5 is one of the major constituents of cytoplasmic polypeptides in neurons. The antigen seems to be expressed almost exclusively in neuronal and neuroendocrine tissues and their neoplasms. PGP 9.5 is also present in undifferentiated embryonic neoplasms like primitive neuroectodermal tumors (PNETs). However, the significance of PGP 9.5 as a marker in diagnostic (neuro-) oncology has not been systematically evaluated yet. In the present study the sensitivity and specificity of the widely used antiserum against PGP 9.5 has been retrospectively examined on 290 formalin-fixed, paraffin-embedded tumors of the nervous system and small round blue cell tumors. The presence of the antigen in tumors of neuronal (24/24) and neuroendocrine (63/73) differentiation confirm PGP 9.5 as a sensitive marker of these tumor groups, particularly in the diagnosis of pituitary adenomas where the expression was neither related to the staining behavior of the tumors in the PAS-orange G-reaction nor to their degree of polypeptide- and glycoprotein hormone activity. The nearly constant immunostaining of medulloblastomas (18/19) and other PNETs (5/6) demonstrate the role of PGP 9.5 as an additional marker in the detection of these embryonic tumors as this peptide was not or only weakly found in glial (11/58), meningeal (5/29), and nerve sheath neoplasms (1/28). On the other hand, the significance in the differential diagnosis of small round blue cell tumors seems to be limited because of positive immunoreactions in neuroblastomas (7/7) and oat cell carcinomas of the lung (7/7) although rhabdomyosarcomas (1/6) and malignant Non-Hodgkin-lymphomas (0/13) react completely negative in our series.

摘要

蛋白基因产物(PGP)9.5极有可能与泛素羧基末端水解酶同工酶L1(UCH-L1)相同,是神经元细胞质多肽的主要成分之一。该抗原似乎几乎仅在神经元和神经内分泌组织及其肿瘤中表达。PGP 9.5也存在于未分化的胚胎肿瘤中,如原始神经外胚层肿瘤(PNETs)。然而,PGP 9.5作为诊断性(神经)肿瘤学标志物的意义尚未得到系统评估。在本研究中,对290例福尔马林固定、石蜡包埋的神经系统肿瘤和小圆形蓝细胞肿瘤,回顾性检测了广泛使用的抗PGP 9.5抗血清的敏感性和特异性。神经元分化肿瘤(24/24)和神经内分泌分化肿瘤(63/73)中抗原的存在证实PGP 9.5是这些肿瘤组的敏感标志物,特别是在垂体腺瘤的诊断中,其表达既与肿瘤在PAS-橙G反应中的染色行为无关,也与其多肽和糖蛋白激素活性程度无关。髓母细胞瘤(18/19)和其他PNETs(5/6)几乎恒定的免疫染色表明PGP 9.5作为这些胚胎肿瘤检测中的附加标志物的作用,因为在胶质细胞瘤(11/58)、脑膜瘤(5/29)和神经鞘瘤(1/28)中未发现或仅微弱发现该肽。另一方面,在小圆形蓝细胞肿瘤的鉴别诊断中的意义似乎有限,因为神经母细胞瘤(7/7)和肺燕麦细胞癌(7/7)中有阳性免疫反应,尽管横纹肌肉瘤(1/6)和恶性非霍奇金淋巴瘤(0/13)在我们的系列中反应完全阴性。

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