Invasive properties of cadmium-resistant human fibrosarcoma HT-1080 cells.

Cancer biochemistry biophysics Pub Date : 1997-06-01
A Haga, H Nagase, H Kito, T Sato
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Abstract

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.

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抗镉人纤维肉瘤HT-1080细胞的侵袭性研究
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细胞中选择抗镉(Cd-R)细胞。HT-1080 Cd-R细胞胞浆中总金属硫蛋白水平显著高于原细胞系,对顺铂和重金属的细胞毒性具有较高的抗性。HT-1080 Cd-R细胞对重组基膜基质具有较高的侵袭性。而HT-1080 Cd-R细胞的运动能力较差。HT-1080和HT-1080 Cd-R细胞对细胞外基质蛋白的粘附能力无显著差异。HT-1080 Cd-R细胞的高侵袭性是由其极强的酶活性引起的。在HT-1080 Cd-R细胞的条件培养基中检测到高水平的92kDa基质金属蛋白酶-9 (MMP-9),而在两种细胞系中分泌的72kDa MMP-2相同。我们的研究表明,通过细胞金属耐受机制获得的耐药可能促进肿瘤化疗期间的恶性和肿瘤转移。
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