Moilanen M, Pirilä E, Grénman R, Sorsa T, Salo T
Department of Diagnostics and Oral Medicine, Institute of Dentistry, University of Oulu, Finland.
J Pathol. 2002 May;197(1):72-81. doi: 10.1002/path.1078.
MMP-8 (collagenase-2) is the most effective collagenase to initiate type I collagen degradation. Since initiation of lysis of the surrounding collagen matrix is an essential prerequisite for carcinoma cells to spread, this study investigated the expression of MMP-8 in squamous cell carcinoma (SCC) of the head and neck in vivo and in vitro. Most of the recently established head and neck carcinoma cell lines (22/25), corresponding tumour (5/7) and dermal (2/2) fibroblasts, commercial tongue carcinoma (HSC-3 and SCC-25), and transformed keratinocyte cell lines of the tongue (IHGK) and skin (HaCaT) expressed MMP-8 mRNA analysed by the PCR method. Western blotting revealed a latent 50 kD band in concentrated culture media of carcinoma cells and corresponding tumour and dermal fibroblasts. The expression of immunoreactive MMP-8 protein was reduced 30% by transforming growth factor beta-1 (TGF-beta1) at 1 ng/ml concentration and 60% at 10 ng/ml concentration, but up-regulated 2- and 2.5-fold after 10 nM and 100 nM phorbol 12-myristate 13 acetate (PMA), respectively. Immunohistological staining localized MMP-8 protein in a few malignant invading tumour cell islands, certain fibroblasts, polymorphonuclear neutrophils (PMNs), and plasma cells. In situ hybridization revealed a faint sporadic signal in carcinoma cells of all eight tissue sections analysed. It is concluded that tissue from head and neck carcinomas can express MMP-8 both in vivo and in vitro. Since the amount of MMP-8 in carcinoma and stromal cells is rather low, MMP-8 may have a potential role, with other collagenases, in the proteolysis of connective tissue associated with the spreading of invasive carcinoma.
基质金属蛋白酶-8(胶原酶-2)是启动I型胶原降解最有效的胶原酶。由于周围胶原基质溶解的启动是癌细胞扩散的必要前提,本研究在体内和体外研究了基质金属蛋白酶-8在头颈部鳞状细胞癌(SCC)中的表达。通过PCR方法分析,大多数最近建立的头颈部癌细胞系(22/25)、相应的肿瘤(5/7)和真皮(2/2)成纤维细胞、商品化舌癌细胞系(HSC-3和SCC-25)以及舌(IHGK)和皮肤(HaCaT)的转化角质形成细胞系均表达基质金属蛋白酶-8 mRNA。蛋白质印迹法显示癌细胞、相应肿瘤和真皮成纤维细胞的浓缩培养基中存在一条潜在的50 kD条带。1 ng/ml浓度的转化生长因子β-1(TGF-β1)可使免疫反应性基质金属蛋白酶-8蛋白的表达降低30%,10 ng/ml浓度时降低60%,但在10 nM和100 nM佛波酯12-肉豆蔻酸酯13-乙酸酯(PMA)作用后分别上调2倍和2.5倍。免疫组织化学染色将基质金属蛋白酶-8蛋白定位于少数恶性侵袭性肿瘤细胞岛、某些成纤维细胞、多形核中性粒细胞(PMN)和浆细胞中。原位杂交显示在所有分析的八个组织切片的癌细胞中均有微弱的散在信号。结论是头颈部癌组织在体内和体外均可表达基质金属蛋白酶-8。由于癌组织和基质细胞中基质金属蛋白酶-8的含量相当低,基质金属蛋白酶-8可能与其他胶原酶一起在与浸润性癌扩散相关的结缔组织蛋白水解中发挥潜在作用。