...
首页> 外文期刊>American Journal of Cancer Research >MicroRNA-506 suppresses invasiveness and metastasis of human hepatocellular carcinoma cells by targeting IL8
【24h】

MicroRNA-506 suppresses invasiveness and metastasis of human hepatocellular carcinoma cells by targeting IL8

机译:MicroRNA-506通过靶向IL8抑制人肝癌细胞的侵袭和转移

获取原文
           

摘要

MicroRNAs (miRNAs) have been reported to be involved in tumor metastasis. In this study, we investigated the function of miR-506 in the metastasis of human hepatocellular carcinoma (HCC). We found that miR-506 is significantly downregulated in the primary tissue of metastatic HCC and in highly metastatic HCC cell lines. Overexpression of miR-506 suppressed HCC cell migration, invasion, and metastasis both in vitro and in vivo. Furthermore, miR-506 was found to specifically target the 3’ untranslated region (3’-UTR) of interleukin 8 (IL8) mRNA. Spearman’s correlation analysis revealed that miR-506 expression inversely correlated with IL8 mRNA and protein expression in HCC tissue samples. IL8 treatment reversed miR-506-induced suppression of HCC cell migration and invasiveness. Thus, miR-506 acts as a tumor suppressor that may inhibit the migration, invasiveness, and metastasis of HCC cells by targeting IL8.
机译:据报道,MicroRNA(miRNA)参与肿瘤转移。在这项研究中,我们调查了miR-506在人类肝细胞癌(HCC)转移中的功能。我们发现,miR-506在转移性HCC的主要组织和高度转移性HCC细胞系中显着下调。在体外和体内,miR-506的过表达均抑制了HCC细胞的迁移,侵袭和转移。此外,发现miR-506特异性靶向白介素8(IL8)mRNA的3'非翻译区(3'-UTR)。 Spearman的相关分析表明,miR-506表达与HCC组织样本中的IL8 mRNA和蛋白质表达呈负相关。 IL8治疗逆转了miR-506诱导的HCC细胞迁移和侵袭性抑制。因此,miR-506充当肿瘤抑制因子,可通过靶向IL8抑制HCC细胞的迁移,侵袭和转移。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号