Zajc Irena, Sever Natasa, Bervar Ales, Lah Tamara T
Department of Genetic Toxicology and Cancer Biology, National Institute of Biology, Vecna pot 111, 1000 Ljubljana, Slovenia.
Cancer Lett. 2002 Dec 10;187(1-2):185-90. doi: 10.1016/s0304-3835(02)00452-4.
The in vitro invasiveness of human breast cancer cell lines was compared with their reported tumorigenicity in vivo, increasing from MCF7, MDA-MB468, MDA-MB231 to MDA-MB435 cells. The invasiveness roughly corresponded to the tumorigenicity of the cell lines. The levels of cathepsin L mRNA and protein correlated with the invasiveness of the cells. Stefin A protein decreased with the invasiveness and the reported tumorigenicity, whereas stefin B protein was significantly lower in all MDA-MB lines compared with the least invasive and tumorigenic MCF7 line. Our results suggest that the imbalance between cathepsin L and the stefins contributes to the development of a malignant cell phenotype.
将人乳腺癌细胞系的体外侵袭性与其在体内已报道的致瘤性进行比较,侵袭性从MCF7、MDA - MB468、MDA - MB231至MDA - MB435细胞逐渐增加。侵袭性大致与细胞系的致瘤性相对应。组织蛋白酶L的mRNA和蛋白质水平与细胞的侵袭性相关。丝抑蛋白A的蛋白质水平随侵袭性和已报道的致瘤性降低,而与侵袭性和致瘤性最低的MCF7细胞系相比,所有MDA - MB细胞系中的丝抑蛋白B蛋白质水平均显著较低。我们的结果表明,组织蛋白酶L和丝抑蛋白之间的失衡促成了恶性细胞表型的发展。