...
首页> 外文期刊>Cell death & disease. >miR-143-3p targeting of ITGA6 suppresses tumour growth and angiogenesis by downregulating PLGF expression via the PI3K / AKT pathway in gallbladder carcinoma
【24h】

miR-143-3p targeting of ITGA6 suppresses tumour growth and angiogenesis by downregulating PLGF expression via the PI3K / AKT pathway in gallbladder carcinoma

机译:靶向ITGA6的miR-143-3p可通过PI3K / AKT途径下调PLGF在胆囊癌中的表达来抑制肿瘤的生长和血管生成

获取原文
           

摘要

Gallbladder cancer (GBC) is the most common malignant tumour of the biliary track system. Angiogenesis plays a pivotal role in the development and progression of malignant tumours. miR-143-3p acts as a tumour suppressor in various cancers. Their role in GBC is however less well defined. Here we show that the expression levels of miR-143-3p were decreased in human GBC tissues compared with the non-tumour adjacent tissue (NAT) counterparts and were closely associated with overall survival. We discovered that miR-143-3p was a novel inhibitor of tumour growth and angiogenesis in vivo and in vitro. Our antibody array, ELISA and PLGF rescue analyses indicated that PLGF played an essential role in the antiangiogenic effect of miR-143-3p. Furthermore, we used miRNA target-prediction software and dual-luciferase assays to confirm that integrin α6 (ITGA6) acted as a direct target of miR-143-3p. Our ELISA and western blot analyses confirmed that the expression of PLGF was decreased via the ITGA6/PI3K/AKT pathway. In conclusion, miR-143-3p suppresses tumour angiogenesis and growth of GBC through the ITGA6/PI3K/AKT/PLGF pathways and may be a novel molecular therapeutic target for GBC.
机译:胆囊癌(GBC)是胆道系统最常见的恶性肿瘤。血管生成在恶性肿瘤的发生和发展中起关键作用。 miR-143-3p在各种癌症中起着抑癌作用。但是,它们在GBC中的作用尚不明确。在这里,我们显示与非肿瘤邻近组织(NAT)对应物相比,人GBC组织中miR-143-3p的表达水平有所降低,并且与总体存活率密切相关。我们发现miR-143-3p是体内和体外肿瘤生长和血管生成的新型抑制剂。我们的抗体阵列,ELISA和PLGF拯救分析表明PLGF在miR-143-3p的抗血管生成作用中起着至关重要的作用。此外,我们使用miRNA靶标预测软件和双荧光素酶测定法来确认整合素α6(ITGA6)是miR-143-3p的直接靶标。我们的ELISA和Western blot分析证实PLGF的表达通过ITGA6 / PI3K / AKT途径降低。总之,miR-143-3p通过ITGA6 / PI3K / AKT / PLGF途径抑制肿瘤血管生成和GBC的生长,可能是GBC的新型分子治疗靶标。

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