4.7 Article

MicroRNA-196a is regulated by ER and is a prognostic biomarker in ER plus breast cancer

期刊

BRITISH JOURNAL OF CANCER
卷 120, 期 6, 页码 621-632

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/s41416-019-0395-8

关键词

-

类别

资金

  1. Cancer Research UK
  2. British Columbia Cancer Agency Branch
  3. National Breast Cancer Foundation [2012002037]
  4. National Health and Medical Research Council [AP1058421, AP1106907]
  5. University of Queensland
  6. Tenovus Cancer Care Charity
  7. Breast Cancer Now Fellowship
  8. Cardiff University
  9. National Institute of Heath [CA1130001]

向作者/读者索取更多资源

BACKGROUND: MicroRNAs are potent post-transcriptional regulators involved in all hallmarks of cancer. Mir-196a is transcribed from two loci and has been implicated in a wide range of developmental and pathogenic processes, with targets including Hox, Fox, Cdk inhibitors and annexins. Genetic variants and altered expression of MIR196A are associated with risk and progression of multiple cancers including breast cancer, however little is known about the regulation of the genes encoding this miRNA, nor the impact of variants therein. METHODS: Genomic data and chromatin interaction analysis were used to discover functional promoter and enhancer elements for MIR196A. Expression data were used to associate MIR196A with mechanisms of resistance, breast cancer subtypes and prognosis. RESULTS: Here we demonstrate that MIR196A displays complex and dynamic expression patterns, in part controlled by long-range transcriptional regulation between promoter and enhancer elements bound by ERa. Expression of this miRNA is significantly increased in drug-resistant models of hormone-receptor positive disease. The expression of MIR196A also proves to be a robust prognostic factor for patients with advanced and post-menopausal ER+ disease. CONCLUSION: This work sheds light on the normal and abnormal regulation of MIR196A and provides a novel stratification method for therapeutically resistant breast cancer.

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

4.7
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