Natkunam Y, Warnke R A, Montgomery K, Falini B, van De Rijn M
Department of Pathology, Stanford University Medical Center, Stanford, California 94305, USA.
Mod Pathol. 2001 Jul;14(7):686-94. doi: 10.1038/modpathol.3880373.
The gene encoding MUM1 was characterized as a possible translocation partner in chromosomal abnormalities involving a significant number of multiple myelomas. The overexpression of the MUM1 protein as a result of translocation t(6;14) (p25;q32) identified MUM1 as a putative regulatory molecule involved in B-cell differentiation and tumorigenesis. The expression of MUM1 protein in multiple myelomas supports this hypothesis. In the current study, using tissue microarray technology, we have tested the expression of the MUM1 protein in 1335 human malignancies and normal tissues. Our data show that the MUM1 protein is expressed in a wide spectrum of hematolymphoid neoplasms and in malignant melanomas but is absent in other human tumors. In addition, in tissue microarrays as well as in conventional paraffin sections, MUM1 staining was found to lack specificity in detecting plasmacytic differentiation as compared with two markers, CD138/Syndecan and VS38, commonly used in paraffin immunohistochemistry for detection of plasma cells.
编码MUM1的基因被鉴定为可能是涉及大量多发性骨髓瘤的染色体异常中的易位伙伴。由于t(6;14)(p25;q32)易位导致MUM1蛋白过表达,这表明MUM1是一种参与B细胞分化和肿瘤发生的假定调节分子。MUM1蛋白在多发性骨髓瘤中的表达支持了这一假说。在本研究中,我们使用组织芯片技术检测了1335例人类恶性肿瘤和正常组织中MUM1蛋白的表达。我们的数据表明,MUM1蛋白在广泛的血液淋巴系统肿瘤和恶性黑色素瘤中表达,但在其他人类肿瘤中不存在。此外,与石蜡免疫组织化学中常用的两种检测浆细胞的标记物CD138/多配体蛋白聚糖和VS38相比,在组织芯片以及传统石蜡切片中,发现MUM1染色在检测浆细胞分化方面缺乏特异性。