Bonfil R D, Farías E, Ruggeri B
Laboratorio de la Fundación de Investigación del Cáncer (FUNDIC), Centro de Estudios Farmacológicos y Botánicos (CEFYBO-CONICET) Serrano 669, Buenos Aires, Argentina.
Acta Physiol Pharmacol Ther Latinoam. 1995;45(3):185-91.
Twelve immortalized human cell lines derived from primary or metastatic lesions from pancreatic carcinomas were studied with respect to their in vitro invasiveness and motility. Various levels of invasive capacity and chemotactic responses were found. Zymograms of cells conditioned media were carried out to determine the role of metalloproteinases in pancreatic cancer invasion. No correlations were found, however, between invasive capacity of pancreatic carcinoma cell lines and gelatinase secretion. Putative reasons for these findings are discussed.
对源自胰腺癌原发或转移病灶的12种永生化人类细胞系的体外侵袭性和运动性进行了研究。发现了不同水平的侵袭能力和趋化反应。对细胞条件培养基进行酶谱分析以确定金属蛋白酶在胰腺癌侵袭中的作用。然而,未发现胰腺癌细胞系的侵袭能力与明胶酶分泌之间存在相关性。讨论了这些发现的可能原因。