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Inhibitory effects of c9t11-conjugated linoleic acid on invasion of human gastric carcinoma cell line SGC-7901

机译:c9t11共轭亚油酸对人胃癌细胞SGC-7901侵袭的抑制作用

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摘要

AIM: To investigate the effect of c9,t11-conjugated linoleic acid (c9,t11-CLA) on the invasion of human gastric carcinoma cell line and its possible mechanism of preventing metastasis.METHODS: Using reconstituted basement membrane invasion, chemotaxis, adhesion, PAGE substrate zymography and RT-PCR assays, we analyzed the abilities of invasion, direct migration, adhesion of intracellular matrix, as well as the activity of type IV collagenase and expression of tissue inhibitor of metalloproteinase (TIMP)-1 and TIMP-2 mRNA in SGC-7901 cells which were treated with gradually increased concentrations (25, 50, 100 and 200 μmol/L) of c9,t11-CLA for 24 h.RESULTS: At the concentrations of 200 μmol/L, 100 μmol/L and 50 μmol/L, c9,t11-CLA suppressed the invasion of SGC-7901 cells into the reconstituted basement membrane by 53.7%, 40.9% and 29.3%, respectively, in comparison with the negative control. Only in the 200 μmol/L c9,t11-CLA group, the chemotaxis of SGC-7901 cells was inhibited by 16.0% in comparision with the negative control. C9,t11-CLA also could inhibit the adhesion of SGC-7901 cells to laminin, fibronectin and Matrigel, increase the expression of TIMP-1 and TIMP-2 mRNA, and reduce type IV collagenase activities in the serum-free medium supernatant of SGC-7901 cells.CONCLUSION: c9,t11-CLA can inhibit the invasion of SGC-7901 cells at multiple procedures in tumor metastasis cascade, which may be associated with the induction of TIMP-1 and TIMP-2 mRNA expression.
机译:目的:探讨c9,t11-共轭亚油酸(c9,t11-CLA)对人胃癌细胞侵袭的影响及其可能的预防转移机制。方法:利用重组基膜侵袭,趋化性,黏附, PAGE底物酶谱和RT-PCR分析,我们分析了侵袭,直接迁移,细胞内基质粘附,IV型胶原酶活性以及组织金属蛋白酶(TIMP)-1和TIMP-2 mRNA表达的能力。在逐渐增加浓度(25、50、100和200μmol/ L)的c9,t11-CLA处理的SGC-7901细胞中处理24小时。结果:在200μmol/ L,100μmol/ L和与阴性对照相比,50μmol/ L,c9,t11-CLA分别抑制SGC-7901细胞侵入重组基底膜的侵袭率分别为53.7%,40.9%和29.3%。仅在200μmol/ L c9,t11-CLA组中,与阴性对照相比,SGC-7901细胞的趋化性被抑制了16.0%。 C9,t11-CLA还可以抑制SGC-7901细胞与层粘连蛋白,纤连蛋白和基质胶的粘附,增加TIMP-1和TIMP-2 mRNA的表达,并降低SGC无血清培养基上清液中的IV型胶原酶活性。结论:c9,t11-CLA可以在肿瘤转移级联的多个过程中抑制SGC-7901细胞的侵袭,这可能与诱导TIMP-1和TIMP-2 mRNA表达有关。

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