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Intestinal trefoil factor promotes invasion in non-tumorigenic Rat-2 fibroblast cell.

机译:肠三叶因子促进非致瘤大鼠2成纤维细胞的侵袭。

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Intestinal trefoil factor (TFF3) is essential in regulating cell migration and maintaining mucosal integrity in gastrointestinal tract. We previously showed that TFF3 was overexpressed in gastric carcinoma. Whether TFF3 possesses malignant potential is not fully elucidated. We sought to investigate the effects of inducting TFF3 expression in a non-malignant rat fibroblast cell line (Rat-2) on the cell proliferation, invasion and the genes regulating cell invasion. Invasiveness and proliferation of transfected Rat-2 cell line were assessed using in vitro invasion chamber assay and colorimetric MTS assay. Differential mRNA expressions of invasion-related genes, namely, metalloproteinases (MMP-9), tissue inhibitors of metalloproteinases (TIMP-1), beta-catenin and E-cadherin, were determined by quantitative real-time polymerase chain reaction (PCR). We showed that TFF3 did not inhibit the proliferation of Rat-2 cells. We also demonstrated that transfection of TFF3 significantly promoted invasion of Rat-2 cells by 1.4- to 2.2-folds. There was an upregulation of beta-catenin (13.1-23.0%) and MMP-9 (43.4-92.2%) mRNA expression levels, and downregulation of E-cadherin (25.6-33.8%) and TIMP-1 (31.5-37.8%) in TFF3-transfected cells compared to controls during 48-h incubation. Our results suggested that TFF3 possesses malignant potential through promotion of cell invasiveness and alteration of invasion-related genes.
机译:肠三叶因子(TFF3)在调节细胞迁移和维持胃肠道粘膜完整性中至关重要。我们以前表明,TFF3在胃癌中过表达。 TFF3是否具有恶性潜力尚未完全阐明。我们试图研究在非恶性大鼠成纤维细胞系(Rat-2)中诱导TFF3表达对细胞增殖,侵袭和调节细胞侵袭基因的影响。使用体外侵袭室测定法和比色MTS测定法评估转染的Rat-2细胞系的侵袭性和增殖。通过定量实时聚合酶链反应(PCR)测定入侵相关基因的差异mRNA表达,即金属蛋白酶(MMP-9),金属蛋白酶组织抑制剂(TIMP-1),β-连环蛋白和E-钙粘蛋白。我们表明,TFF3不会抑制Rat-2细胞的增殖。我们还证明了转染TFF3可以显着促进大鼠2细胞侵袭1.4到2.2倍。 β-catenin(13.1-23.0%)和MMP-9(43.4-92.2%)mRNA表达水平上调,E-cadherin(25.6-33.8%)和TIMP-1(31.5-37.8%)下调。在48小时的温育过程中,与对照相比,TFF3转染的细胞中的Bcl-2含量更高。我们的结果表明,TFF3通过促进细胞侵袭性和改变侵袭相关基因具有恶性潜能。

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