School of Chemistry and Molecular Biosciences, University of Queensland, St Lucia, QLD, Australia.
ACRF Stem Cells and Cancer, The Walter and Eliza Hall Institute of Medical Research, Parkville, VIC, Australia.
Br J Cancer. 2019 Mar;120(6):621-632. doi: 10.1038/s41416-019-0395-8. Epub 2019 Feb 20.
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.
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.
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 ERα. 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.
This work sheds light on the normal and abnormal regulation of MIR196A and provides a novel stratification method for therapeutically resistant breast cancer.
MicroRNAs 是一种强有力的转录后调控因子,参与癌症的所有标志性特征。Mir-196a 由两个基因座转录,与广泛的发育和致病过程有关,其靶标包括 Hox、Fox、Cdk 抑制剂和膜联蛋白。MIR196A 的遗传变异和表达改变与多种癌症(包括乳腺癌)的风险和进展有关,然而,关于编码这种 miRNA 的基因的调控以及其中变体的影响知之甚少。
使用基因组数据和染色质相互作用分析来发现 MIR196A 的功能启动子和增强子元件。使用表达数据将 MIR196A 与耐药机制、乳腺癌亚型和预后相关联。
在这里,我们证明了 MIR196A 显示出复杂和动态的表达模式,部分受 ERα 结合的启动子和增强子元件之间的长距离转录调控控制。这种 miRNA 的表达在激素受体阳性疾病的耐药模型中显著增加。MIR196A 的表达也被证明是晚期和绝经后 ER+疾病患者的一个稳健的预后因素。
这项工作阐明了 MIR196A 的正常和异常调控,并为治疗耐药性乳腺癌提供了一种新的分层方法。