Ueda M, Fujii H, Yoshizawa K, Terai Y, Kumagai K, Ueki K, Ueki M
Department of Obstetrics and Gynecology, Osaka Medical College, Takatsuki, Osaka, Japan.
Invasion Metastasis. 1998;18(4):176-83. doi: 10.1159/000024510.
Uterine cervical adenocarcinoma typically is an aggressive neoplasm with a propensity for early invasion and dissemination; however, the regulatory mechanism of invasive activity of cervical adenocarcinoma cells has not been fully understood. In this study, biological effects of epidermal growth factor (EGF) and transforming growth factor (TGF)-alpha on invasion and proteinase expression of human cervical adenocarcinoma OMC-4 cells were investigated. Tumor cell migration along a gradient of substratum-bound fibronectin and invasion into the reconstituted basement membrane were stimulated by 0.1-10 nM EGF and TGF-alpha in a concentration-dependent manner. Their effects on tumor cell migration were also confirmed by wound assay. The zymography of tumor-conditioned medium showed that the treatment of OMC-4 cells with EGF and TGF-alpha resulted in the increase of matrix metalloproteinase (MMP)-2 and urokinase-type plasminogen activator (uPA). Matrilysin (MMP-7), also secreted by OMC-4 cells, was not affected by these growth factors. These results suggest that EGF and TGF-alpha act as positive regulators on the invasion of cervical adenocarcinoma cells, which may be associated with their stimulatory effects on tumor cell motility and the induction of type IV collagenase and uPA secreted by tumor cells.
子宫颈腺癌通常是一种侵袭性肿瘤,易于早期侵袭和扩散;然而,宫颈腺癌细胞侵袭活性的调控机制尚未完全阐明。本研究探讨了表皮生长因子(EGF)和转化生长因子(TGF)-α对人宫颈腺癌OMC-4细胞侵袭及蛋白酶表达的生物学效应。0.1 - 10 nM的EGF和TGF-α以浓度依赖的方式刺激肿瘤细胞沿基质结合纤连蛋白梯度迁移并侵入重组基底膜。伤口实验也证实了它们对肿瘤细胞迁移的影响。肿瘤条件培养基的酶谱分析表明,用EGF和TGF-α处理OMC-4细胞导致基质金属蛋白酶(MMP)-2和尿激酶型纤溶酶原激活剂(uPA)增加。OMC-4细胞分泌的基质溶素(MMP-7)不受这些生长因子影响。这些结果表明,EGF和TGF-α作为宫颈腺癌细胞侵袭的正调节因子,这可能与其对肿瘤细胞运动性的刺激作用以及对肿瘤细胞分泌的IV型胶原酶和uPA的诱导有关。