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GNAI3 inhibits tumor cell migration and invasion and is post-transcriptionally regulated by miR-222 in hepatocellular carcinoma

机译:GNAI3抑制肿瘤细胞迁移和侵袭,并在肝细胞癌中受miR-222转录后调控

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摘要

Guanine nucleotide binding protein, alpha inhibiting activity polypeptide 3 (GNAI3) is involved in many biological processes. However, its biological function in hepatocellular carcinoma (HCC) remains unclear. An immunohistochemical staining analysis revealed that GNAI3 protein was down-regulated in HCC compared to non-cancerous liver. Furthermore, transwell assays indicated that GNAI3 inhibits HCC cell migration and invasion. Using software predictions and experimental screening, we found that miR-222 could directly bind to GNAI3 mRNA and decrease GNAI3 protein expression in HCC cells. Moreover, miR-222 was up-regulated in HCC and negatively correlated with GNAI3 protein expression. These results indicated that down-regulation of GNAI3 might be caused by up-regulation of miR-222 in HCC In conclusion, GNAI3 was down-regulated by miR-222 in HCC, and this deregulation promoted migration and invasion of HCC. These findings extended our insight into the complex molecular mechanisms underlying the invasion and metastasis of HCC and may provide new therapeutic targets. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
机译:鸟嘌呤核苷酸结合蛋白,α抑制活性多肽3(GNAI3)参与许多生物学过程。但是,其在肝细胞癌(HCC)中的生物学功能仍不清楚。免疫组织化学染色分析显示,与非癌性肝相比,肝癌中GNAI3蛋白被下调。此外,transwell分析表明GNAI3抑制HCC细胞迁移和侵袭。使用软件预测和实验筛选,我们发现miR-222可以直接结合GNAI3 mRNA,并降低HCC细胞中GNAI3蛋白的表达。此外,miR-222在肝癌中上调,与GNAI3蛋白表达呈负相关。这些结果表明,GNAI3的下调可能是由于肝癌中miR-222的上调所致。总之,GNAI3被miR-222在肝癌中的表达下调,这种去激活促进了肝癌的迁移和侵袭。这些发现扩展了我们对肝癌侵袭和转移的复杂分子机制的认识,并可能提供新的治疗靶点。 (C)2014 Elsevier Ireland Ltd.保留所有权利。

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