Zheng W Q, Looi L M, Cheah P L
Department of Pathology, Changhai Hospital, Second Military Medical University, Shanghai, China.
Pathology. 2001 Aug;33(3):303-6.
The basement membrane (BM), of which laminin is a major glycoprotein component, is an important barrier to tumour cells which must be breeched before metastatic spread can occur. We have compared the pattern of laminin expression in a range of benign and malignant breast lesions to better understand the process of tumour progression. A total of 162 cases of breast samples, comprising 18 fibroadenomas, 22 cases of fibrocystic disease, 96 cases of invasive ductal carcinoma and 26 carcinomas with intraductal components, were evaluated for laminin expression by a standard immunoperoxidase method on formalin-fixed, paraffin-embedded histological sections, using a commercial antibody against human laminin. The pattern of laminin expression was charted as follows: Type I, > 70% of BM complete/continuous; Type II, > 70% of BM moderately disrupted; Type III, > 70% of BM completely disrupted. The Type I pattern was observed in all cases of fibroadenoma and fibrocystic diseases, and in 77% of intraductal carcinoma components. Various patterns of BM disruption were observed in invasive ductal carcinoma. Severity of BM disruption correlated with histological grade of the carcinomas (P < 0.001). Small-sized tumours, those without lymphatic invasion and lymph node-negative tumours showed more complete patterns of laminin expression. The current study suggests that tumour cells with high histological grade possess an enhanced capacity to disrupt the basement membrane, an important step in the metastatic process. The detection of BM disruption by immunohistochemical staining for laminin is technically easy and may be usefully applied for the differentiation of in situ and microinvasive carcinoma.
基底膜(BM)以层粘连蛋白作为主要糖蛋白成分,是肿瘤细胞的重要屏障,肿瘤细胞在发生转移扩散前必须突破该屏障。我们比较了一系列良性和恶性乳腺病变中层粘连蛋白的表达模式,以更好地了解肿瘤进展过程。通过标准免疫过氧化物酶方法,使用抗人层粘连蛋白的商业抗体,对162例乳腺样本进行层粘连蛋白表达评估,这些样本包括18例纤维腺瘤、22例纤维囊性疾病、96例浸润性导管癌和26例伴有导管内成分的癌,样本均为经福尔马林固定、石蜡包埋的组织学切片。层粘连蛋白的表达模式记录如下:I型,>70%的基底膜完整/连续;II型,>70%的基底膜中度破坏;III型,>70%的基底膜完全破坏。在所有纤维腺瘤和纤维囊性疾病病例以及77%的导管内癌成分中观察到I型模式。在浸润性导管癌中观察到基底膜破坏的各种模式。基底膜破坏的严重程度与癌的组织学分级相关(P<0.001)。小尺寸肿瘤、无淋巴浸润的肿瘤和淋巴结阴性肿瘤显示出更完整的层粘连蛋白表达模式。当前研究表明,具有高组织学分级的肿瘤细胞具有更强的破坏基底膜的能力,这是转移过程中的重要一步。通过层粘连蛋白免疫组织化学染色检测基底膜破坏在技术上很容易,并且可有效地用于原位癌和微浸润癌的鉴别。