妇科肿瘤中新的膜相关胎盘组织蛋白(mp2a, B, C, D和E)的免疫组织化学和超微结构研究

Y Hirai, N Inaba, H Takamizawa, J T Chen, K Hasumi, K Masubuchi, H Bohn, H Suemizu, Y Osamura, K Watanabe
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引用次数: 0

摘要

应用亲和素-生物素免疫过氧化物酶技术和免疫电镜对不同妇科肿瘤和正常妇科组织中新的胎盘膜相关蛋白(mp2a、B、C、D、E)进行免疫组化研究。mp2a和mp2b对恶性肿瘤无特异性。mp2c存在于67-100%的卵巢癌、100%的良性皮样囊肿和77%的子宫内膜癌中。除宫颈腺癌外,MP2在妇科恶性肿瘤中几乎检测不到。尽管mp2e在妇科良性肿瘤中几乎检测不到,但该蛋白在卵巢癌、子宫鳞癌、宫颈内膜腺癌和子宫内膜腺癌中均存在。这些结果提示MP2蛋白作为妇科恶性肿瘤新标志物的临床应用前景。
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Immunohistochemical and ultrastructural investigation of new membrane-associated placental tissue proteins (MP2 A, B, C, D, and E) in gynecologic neoplasms.

New membrane-associated placental tissue proteins (MP2 A, B, C, D, and E) were investigated immunohistochemically by avidin-biotin immunoperoxidase technique and immunoelectron microscopy in various gynecologic neoplasms and normal gynecologic tissues. MP2 A and MP2 B were not specific for malignant tumors. MP2 C was present in 67-100% of ovarian carcinomas, 100% of benign dermoid cysts, and 77% of endometrial carcinomas. Except for endocervical adenocarcinomas, MP2 D was hardly detectable in gynecologic malignancies. Although MP2 E was hardly detectable in benign gynecologic tumors, this protein was present in ovarian carcinomas, uterine squamous carcinomas, endocervical adenocarcinomas, and endometrial adenocarcinomas. These results suggest a possible clinical application of these MP2 proteins as a new tumor marker for gynecologic malignancies.

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