...
首页> 外文期刊>Biomedicine & pharmacotherapy =: Biomedecine & pharmacotherapie >miR-101 represses lung cancer by inhibiting interaction of fibroblasts and cancer cells by down-regulating CXCL12
【24h】

miR-101 represses lung cancer by inhibiting interaction of fibroblasts and cancer cells by down-regulating CXCL12

机译:miR-101通过下调CXCL12抑制成纤维细胞与癌细胞的相互作用来抑制肺癌

获取原文
获取原文并翻译 | 示例

摘要

Cancer-associated fibroblasts (CAFs) are the main component of tumor stroma which support tumor progression. Here, we set out to determine the factors that may be involved in dramatic alteration of microRNAs (miRNAs) expression pattern in CAFs. miRNAs analyses identified differential expression of 15 microRNAs, with miR-101 being the most downregulated miRNA in CAFs which were different from the normal fibroblasts. We examined several putative miR-101 target genes identified by microarray analysis and demonstrated that miR-101 directly targets CXCL12, which play important roles in CAFs. Overexpression of miR-101 significantly impaired the ability of CAFs to stimulate tumor cell proliferation, sphere formation migration and invasion, and enhanced apoptosis. Further research showed that the cellular biological behavior was regulated by miR-101 targeting CXCL12. These findings provide new insights miR-101 down-regulation in CAFs could inhibit lung cancer proliferation and metastasis via targeting CXCL12. (C) 2015 Elsevier Masson SAS. All rights reserved.
机译:癌症相关成纤维细胞(CAF)是支持肿瘤进展的肿瘤基质的主要成分。在这里,我们着手确定可能与CAFs中microRNA(miRNA)表达模式急剧变化有关的因素。 miRNA分析确定了15种microRNA的差异表达,其中miR-101是CAF中表达最下调的miRNA,与正常的成纤维细胞不同。我们检查了通过微阵列分析鉴定的几种推定的miR-101靶基因,并证明miR-101直接靶向CXCL12,后者在CAF中起重要作用。 miR-101的过表达显着削弱了CAF刺激肿瘤细胞增殖,球形成迁移和侵袭的能力,并增强了细胞凋亡。进一步的研究表明,靶向CXCL12的miR-101调节细胞生物学行为。这些发现为CAF中miR-101的下调通过靶向CXCL12抑制肺癌的增殖和转移提供了新的见解。 (C)2015 Elsevier Masson SAS。版权所有。

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