4.5 Article

miRNA-542-3p downregulation promotes trastuzumab resistance in breast cancer cells via AKT activation

期刊

ONCOLOGY REPORTS
卷 33, 期 3, 页码 1215-1220

出版社

SPANDIDOS PUBL LTD
DOI: 10.3892/or.2015.3713

关键词

miRNA-542-3p; trastuzumab; drug resistance; AKT

类别

资金

  1. National Science and Technology Support Program [2013BAI09B08]
  2. Tianjin Municipal Major Scientific and Technological Special Project for Significant Anticancer Development [12ZCDZSY15700]

向作者/读者索取更多资源

Trastuzumab (Herceptin) has been widely used in breast cancer treatment. However, the majority of cancers that initially respond to trastuzumab begin to progress again within 1 year. Despite the high resistance rate, the molecular mechanisms underlying this desease are not well understood. In the present study, microRNA (miRNA-542-3p modulated trastuzumab resistance in SKBR3 and MCF7/Her2 breast cancer cell lines. Trastuzumab induced miRNA-542-3p expression in SKBR3 and MCF7/Her2 cells. Furthermore, knockdown of miRNA-542-3p in the two cell lines resulted in decreased drug sensitivity to trastuzumab and cell apoptosis. The blockage of G1/S checkpoint by trastuzumab was rescued as well. miRNA-542-3p knockdown also activated the phosphatidylinositol 3-kinase (PI3K)-Akt pathway, while LY294002 reversed the effect of miRNA-542-3p knockdown. In summary, the results suggested that miRNA-542-3p downregulation may contribute to the trastuzumab resistance in breast cancer via, at least in part, the PI3K-akt pathway. Our findings provide new molecular mechanisms in trastuzumab resistance.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据