de Roos M A J, van der Vegt B, Peterse J L, Patriarca C, de Vries J, de Bock G H, Wesseling J
Department of Surgical Oncology, University Medical Centre Groningen, University of Groningen, Groningen, The Netherlands.
Histopathology. 2007 Aug;51(2):227-38. doi: 10.1111/j.1365-2559.2007.02754.x.
To classify MUC1 according to five predefined expression patterns in ductal carcinoma in situ (DCIS) and related clinicopathological parameters, coexpression of other biological markers and prognosis.
With a manual tissue arrayer, 92% (n = 80) of the 87 DCIS samples were successfully targeted. Immunohistochemistry was carried out for MUC1, oestrogen receptor (ER), progesterone receptor (PR), Her2/Neu, p53 and cyclin D1. Entire membrane expression was related to Her2/neu negativity (P =0.042). Apical membrane expression was associated with low grade (P = 0.027), Her2/neu negativity (P = 0.014) and PR positivity (P = 0.005). Focal cytoplasmic expression was related to high grade (P = 0.006). Diffuse cytoplasmic expression was associated with high grade (P = 0.004), large tumour size (P = 0.046), Her2/neu positivity (P =0.042) and cyclin D1 positivity (P = 0.002). On the basis of these analyses the four patterns were reclassified as membranous or cytoplasmic expression. On multivariate analysis, cytoplasmic MUC1 expression (hazard ratio 8.5, 95% confidence interval 1.0, 73.0; P = 0.04) was the only independent predictor of local recurrence.
Four patterns of MUC1 expression are recognized in DCIS that suggest a relationship to functional differentiation and can be simplified into two types that are clinically relevant and could therefore be helpful in the distinction between different subgroups of DCIS.
根据导管原位癌(DCIS)中五种预先定义的表达模式、相关临床病理参数、其他生物标志物的共表达情况及预后对MUC1进行分类。
使用手动组织阵列仪,87个DCIS样本中有92%(n = 80)被成功定位。对MUC1、雌激素受体(ER)、孕激素受体(PR)、Her2/Neu、p53和细胞周期蛋白D1进行免疫组织化学检测。全膜表达与Her2/neu阴性相关(P = 0.042)。顶端膜表达与低级别相关(P = 0.027)、Her2/neu阴性相关(P = 0.014)及PR阳性相关(P = 0.005)。局灶性细胞质表达与高级别相关(P = 0.006)。弥漫性细胞质表达与高级别相关(P = 0.004)、肿瘤体积大相关(P = 0.046)、Her2/neu阳性相关(P = 0.042)及细胞周期蛋白D1阳性相关(P = 0.002)。基于这些分析,这四种模式被重新分类为膜性或细胞质表达。多因素分析显示,细胞质MUC1表达(风险比8.5,95%置信区间1.0,73.0;P = 0.04)是局部复发的唯一独立预测因素。
在DCIS中识别出四种MUC1表达模式,提示其与功能分化有关,可简化为两种具有临床相关性的类型,因此有助于区分DCIS的不同亚组。