Muraoka K, Nabeshima K, Kataoka H, Kishi J, Koono M
Department of Pathology, Miyazaki Medical College, Japan.
Urol Int. 1995;54(4):184-90. doi: 10.1159/000282721.
A new human carcinoma cell line, UMK-1, was established from primary urinary bladder carcinoma with histological diagnosis of transitional cell carcinoma grade 2, with squamous and adenocarcinomatous differentiation. These histologic features were maintained in the cultured cells and in xenografted tumors in nude mice. Ultrastructurally, the cultured cells were characterized by formation of glandular structure with well-formed junctional complexes and microvilli, intracytoplasmic lumina and tonofilament bundles. Upon continuous propagation in serum-free medium, UMK-1 cells secreted gelatinases and tissue inhibitor of metalloproteinase (TIMP)-1 into the conditioned medium. The gelatinolytic activities which were inhibited by EDTA, were composed of a major band at 95 kD and a minor band at 68 kD on gelatin zymography. The measurement of TIMP-1 in the conditioned medium was performed by the one-step sandwich enzyme immunoassay system. The production of gelatinases and TIMP-1 was observed during the late log phase of the cell growth and those productions showed similar kinetics. UMK-1 cells can be used to study the interaction of tumor cell-derived gelatinolytic proteinases and TIMP-1 in cancer invasion and metastasis.
一种新的人类癌细胞系UMK-1,是从原发性膀胱癌中建立的,其组织学诊断为2级移行细胞癌,伴有鳞状和腺癌分化。这些组织学特征在培养细胞和裸鼠异种移植瘤中得以保留。在超微结构上,培养细胞的特征是形成具有良好形成的连接复合体和微绒毛、胞质内管腔和张力丝束的腺结构。在无血清培养基中连续传代时,UMK-1细胞将明胶酶和金属蛋白酶组织抑制剂(TIMP)-1分泌到条件培养基中。在明胶酶谱上,被EDTA抑制的明胶水解活性由一条95 kD的主要条带和一条68 kD的次要条带组成。通过一步夹心酶免疫测定系统对条件培养基中的TIMP-1进行测定。在细胞生长的对数后期观察到明胶酶和TIMP-1的产生,并且这些产生表现出相似的动力学。UMK-1细胞可用于研究肿瘤细胞衍生的明胶水解蛋白酶与TIMP-1在癌症侵袭和转移中的相互作用。