Haga A, Nagase H, Kito H, Sato T
Department of Public Health, Gifu Pharmaceutical University, Japan.
Cancer Biochem Biophys. 1997 Jun;15(4):275-84.
Invasive properties of tumor cells having acquired heavy metal resistance were investigated. We selected the cadmium-resistant (Cd-R) cells from human fibrosarcoma HT-1080 cells. Total metallothionein levels in cytosol of HT-1080 Cd-R cells were significantly higher than original lines, and were of a highly resistant potency to cytotoxicity of cisplatin, as well as heavy metals. The HT-1080 Cd-R cells showed higher invasiveness into recombinant basement membrane Matrigel. However, HT-1080 Cd-R cells were inferior in locomotion ability. Significant differences in adhesive ability to extracellular matrix proteins were not observed between HT-1080 and HT-1080 Cd-R cells. High invasiveness of HT-1080 Cd-R cells was caused by their extremely strong enzymatic activities. High level of 92kDa matrix metalloproteinase-9 (MMP-9) was recognized from the conditioned medium of HT-1080 Cd-R cells, whereas 72kDa MMP-2 was secreted equally from both cell lines. Our investigation suggests that drug resistance acquired through the mechanisms of cellular metal-tolerance may promote malignancy and tumor metastasis during cancer chemotherapy.
研究了获得重金属抗性的肿瘤细胞的侵袭特性。我们从人纤维肉瘤HT - 1080细胞中筛选出耐镉(Cd - R)细胞。HT - 1080 Cd - R细胞胞质溶胶中的总金属硫蛋白水平显著高于原始细胞系,并且对顺铂以及重金属的细胞毒性具有高度抗性。HT - 1080 Cd - R细胞对重组基底膜基质胶表现出更高的侵袭性。然而,HT - 1080 Cd - R细胞的运动能力较差。HT - 1080细胞和HT - 1080 Cd - R细胞在对细胞外基质蛋白的黏附能力上未观察到显著差异。HT - 1080 Cd - R细胞的高侵袭性是由其极强的酶活性引起的。从HT - 1080 Cd - R细胞的条件培养基中可检测到高水平的92kDa基质金属蛋白酶 - 9(MMP - 9),而两种细胞系分泌72kDa MMP - 2的水平相当。我们的研究表明,通过细胞金属耐受性机制获得的耐药性可能在癌症化疗期间促进恶性肿瘤和肿瘤转移。