Bièche I, Ruffet E, Zweibaum A, Vildé F, Lidereau R, Franc B
Laboratoire d'Oncogénétique, Centre René Huguenin, Hôpital Ambroise Paré, France.
Thyroid. 1997 Oct;7(5):725-31. doi: 10.1089/thy.1997.7.725.
MUC1 mucin is found in a variety of epithelial tissues and is overexpressed in several epithelial cancers. This molecule could modulate cellular adhesion and thereby influence tumor invasion and metastasis. Little is known of MUC1 gene expression in thyroid tissues. We investigated whether MUC1 mucin gene alteration and/or expression correlated with thyroid tumor progression by studying 21 fresh thyroid tissue specimens comprising 10 macrofollicular adenomas and 11 papillary carcinomas. Normal adjacent tissue from the same patients was also studied. To determine the integrity and expression of the MUC1 mucin gene, a complementary DNA (cDNA) probe was used for Southern blot analysis of DNA and Northern blot analysis of RNA. A detailed immunohistochemical analysis of MUC1 protein expression was performed with DF3 monoclonal antibody, and was compared with other tumor characteristics and clinical manifestations at diagnosis. Of the 14 tumors informative (heterozygous) with the pMUC10 polymorphic probe, 2 (14%) showed loss of heterozygosity (1 adenoma and 1 carcinoma). Overexpression of MUC1 RNA, compared with normal thyroid tissue, was observed in 6 of the 11 papillary carcinomas and in none of the 10 adenomas. Immunostaining of the corresponding formalin-fixed paraffin-embedded tissue sections detected MUC1 mucin protein at the apical domain of follicular cells. Most of the lining was thin in normal tissue and follicular adenomas, but the protein was more irregularly and less strongly expressed in adenomas. In carcinomas the epithelial mucin produced by the MUC1 gene was present irregularly as a thin and/or thick lining at the apical domain of tumor cells. In addition, 5 of the 6 samples with MUC1 mRNA overexpression showed intracytoplasmic staining. Moreover, intracytoplasmic MUC1 mucin staining was found in 75% of "high-risk" papillary thyroid carcinoma (PTC) (PTC with extrathyroid extension at initial diagnosis and/or lymph node involvement), and in only 28.5% of "low-risk" PTC (purely intrathyroidal carcinomas).
粘蛋白1(MUC1)存在于多种上皮组织中,在几种上皮癌中过度表达。该分子可调节细胞粘附,从而影响肿瘤侵袭和转移。关于甲状腺组织中MUC1基因的表达知之甚少。我们通过研究21份新鲜甲状腺组织标本(包括10例大滤泡性腺瘤和11例乳头状癌),调查MUC1粘蛋白基因改变和/或表达是否与甲状腺肿瘤进展相关。还研究了同一患者的正常相邻组织。为了确定MUC1粘蛋白基因的完整性和表达,使用互补DNA(cDNA)探针进行DNA的Southern印迹分析和RNA的Northern印迹分析。用DF3单克隆抗体对MUC1蛋白表达进行了详细的免疫组织化学分析,并与诊断时的其他肿瘤特征和临床表现进行了比较。在14个对pMUC10多态性探针有信息意义(杂合)的肿瘤中,2个(14%)显示杂合性缺失(1例腺瘤和1例癌)。与正常甲状腺组织相比,在11例乳头状癌中有6例观察到MUC1 RNA的过度表达,而10例腺瘤中均未观察到。对相应的福尔马林固定石蜡包埋组织切片进行免疫染色,在滤泡细胞的顶端区域检测到MUC1粘蛋白。在正常组织和滤泡性腺瘤中,大多数内衬较薄,但该蛋白在腺瘤中的表达更不规则且强度较低。在癌中,由MUC1基因产生的上皮粘蛋白不规则地以薄和/或厚的内衬形式存在于肿瘤细胞的顶端区域。此外,6例MUC1 mRNA过度表达的样本中有5例显示胞浆内染色。此外,在75%的“高危”甲状腺乳头状癌(PTC)(初诊时伴有甲状腺外侵犯和/或淋巴结受累的PTC)中发现胞浆内MUC1粘蛋白染色,而在仅28.5%的“低危”PTC(单纯甲状腺内癌)中发现。