Miettinen H, Kononen J, Haapasalo H, Helén P, Sallinen P, Harjuntausta T, Helin H, Alho H
Laboratory of Neurobiology, Medical School, University of Tampere, Finland.
Cancer Res. 1995 Jun 15;55(12):2691-5.
The expression of peripheral-type benzodiazepine receptor (PBR) and diazepam binding inhibitor (DBI) were studied in human astrocytic tumors using immunocytochemistry and in situ hybridization. Both PBR and DBI were prominently expressed in neoplastic cells, whereas in normal brain their amount was low or undetectable. Immunocytochemical double staining demonstrated that PBR and DBI were present in the same cells, suggesting that DBI may act in an autocrine manner in these cells. Analysis of 86 cases showed that PBR expression was statistically significantly associated with tumor malignancy grade (P = 0.004) and the proliferative index as determined by immunocytochemistry with the MIB-1 antibody (P = 0.004). Patients having tumors with high levels of PBR-immunoreactive cells had a shorter life expectancy than patients whose tumors showed lower PBR contents (P = 0.024). In conclusion, these results show that PBR expression is higher in neoplastic cells than in normal brain tissue. They also suggest that PBR immunocytochemistry might be useful in evaluating malignancy in brain tumors.
利用免疫细胞化学和原位杂交技术,对人星形细胞瘤中周边型苯二氮䓬受体(PBR)和地西泮结合抑制剂(DBI)的表达进行了研究。PBR和DBI在肿瘤细胞中均有显著表达,而在正常脑组织中其含量较低或无法检测到。免疫细胞化学双重染色显示PBR和DBI存在于同一细胞中,提示DBI可能在这些细胞中以自分泌方式发挥作用。对86例病例的分析表明,PBR表达与肿瘤恶性程度(P = 0.004)以及用MIB-1抗体通过免疫细胞化学测定的增殖指数(P = 0.004)在统计学上显著相关。PBR免疫反应性细胞水平高的肿瘤患者的预期寿命比肿瘤PBR含量低的患者短(P = 0.024)。总之,这些结果表明,肿瘤细胞中PBR的表达高于正常脑组织。它们还提示PBR免疫细胞化学可能有助于评估脑肿瘤的恶性程度。