Khalid H, Yasunaga A, Kishikawa M, Shibata S
Department of Neurosurgery, Nagasaki University School of Medicine, Japan.
Cancer. 1995 May 15;75(10):2571-8. doi: 10.1002/1097-0142(19950515)75:10<2571::aid-cncr2820751026>3.0.co;2-u.
Expression of the estrogen receptor-related antigen (ER-D5) has been reported in some normal and neoplastic tissues. The authors evaluated the expression of ER-D5 in 143 intracranial tumors of different histologic types.
Formalin fixed, paraffin embedded tumor sections were stained with the monoclonal D5 antibody by avidin-biotin complex immunohistochemistry.
Eighty-eight (62%) of the 143 brain tumors showed positive ER-D5 immunoreactivity. ER-D5 expression was observed in 9/30 low grade astrocytomas, in 6/13 anaplastic astrocytomas, in 16/27 glioblastomas, in 2/5 ependymomas, in 5/8 medulloblastomas, in 10/15 meningiomas, in 20/23 schwannomas, in 11/11 hemangioblastomas, in 9/9 germ cell tumors, in 0/2 oligodendrogliomas, and in 17/28 pediatric and childhood brain tumors. The mean percentage of ER-D5-positive cells varied in different tumor types, was lowest in the meningotheliomatous meningiomas, and was highest in the hemangioblastomas. ER-D5 immunoreactivity was also observed in the microvascular endothelial proliferations and in tumor blood vessels. ER-D5 expression in tumors was not related to the overall tumor grades, but a statistically significant higher percentage of ER-D5-positive cells was noted in the glioblastomas compared with the low grade astrocytomas (P < 0.05) and in the combined high grade tumors compared with the low grade tumors (P < 0.005) if vascular-origin tumor hemangioblastomas are considered a separate entity from other brain tumors.
The current study suggests that the ER-D5 antigen may participate in the growth of the intracranial tumors and tumor angiogenesis. ER-D5 in embryonal and germ cell brain tumors suggests that ER-D5 may be a developmentally regulated protein.
雌激素受体相关抗原(ER-D5)已在一些正常组织和肿瘤组织中被报道。作者评估了143例不同组织学类型的颅内肿瘤中ER-D5的表达情况。
用福尔马林固定、石蜡包埋的肿瘤切片,通过抗生物素蛋白-生物素复合物免疫组织化学法用单克隆D5抗体染色。
143例脑肿瘤中有88例(62%)显示ER-D5免疫反应阳性。在9/30例低级别星形细胞瘤、6/13例间变性星形细胞瘤、16/27例胶质母细胞瘤、2/5例室管膜瘤、5/8例髓母细胞瘤、10/15例脑膜瘤、20/23例神经鞘瘤、11/11例血管母细胞瘤、9/9例生殖细胞肿瘤、0/2例少突胶质细胞瘤以及17/28例儿童和小儿脑肿瘤中观察到ER-D5表达。ER-D5阳性细胞的平均百分比在不同肿瘤类型中有所不同,在脑膜皮型脑膜瘤中最低,在血管母细胞瘤中最高。在微血管内皮增生和肿瘤血管中也观察到ER-D5免疫反应性。肿瘤中的ER-D5表达与总体肿瘤分级无关,但如果将血管源性肿瘤血管母细胞瘤与其他脑肿瘤视为不同实体,则与低级别星形细胞瘤相比,胶质母细胞瘤中ER-D5阳性细胞的百分比具有统计学意义的更高(P < 0.05),与低级别肿瘤相比,在合并的高级别肿瘤中ER-D5阳性细胞的百分比也具有统计学意义的更高(P < 0.005)。
当前研究表明,ER-D5抗原可能参与颅内肿瘤的生长和肿瘤血管生成。胚胎性和生殖细胞脑肿瘤中的ER-D5表明ER-D5可能是一种受发育调节的蛋白。