Mechanisms of endocrine resistance in breast cancer: an overview of the proposed roles of noncoding RNA

被引:147
|
作者
Hayes, Erin L. [1 ,2 ]
Lewis-Wambi, Joan S. [1 ,2 ]
机构
[1] Univ Kansas, Med Ctr, Dept Canc Biol, Kansas City, KS 66160 USA
[2] Univ Kansas, Med Ctr, Dept Physiol, Kansas City, KS 66160 USA
来源
BREAST CANCER RESEARCH | 2015年 / 17卷
基金
美国国家科学基金会;
关键词
ESTROGEN-RECEPTOR-ALPHA; ACTIVATED PROTEIN-KINASE; TAMOXIFEN RESISTANCE; AROMATASE INHIBITOR; GENE-EXPRESSION; ANTIESTROGEN RESISTANCE; SIGNALING PATHWAYS; TUMOR-SUPPRESSOR; DOWN-REGULATION; P-GLYCOPROTEIN;
D O I
10.1186/s13058-015-0542-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Endocrine therapies such as tamoxifen and aromatase inhibitors are the standard treatment options for estrogen receptor-positive breast cancer patients. However, resistance to these agents has become a major clinical obstacle. Potential mechanisms of resistance to endocrine therapies have been identified, often involving enhanced growth factor signaling and changes in the expression or action of the estrogen receptor, but few studies have addressed the role of noncoding RNA (ncRNA). Two important types of ncRNA include microRNA (miRNA) and long noncoding RNA (lncRNA). miRNAs are small RNA molecules that regulate gene expression via translational inhibition or degradation of mRNA transcripts, while lncRNAs are larger RNA molecules that have been shown to play a role in multiple cellular maintenance functions such as protein scaffolding, chromatin looping, and regulation of mRNA stability. Both miRNA and lncRNA have recently impacted the field of breast cancer research as important pieces in the mechanistic puzzle of the genes and pathways involved in breast cancer development and progression. This review serves as an overview of the roles of miRNA and lncRNA in breast cancer progression and the development of endocrine resistance. Ideally, future experiments in the field should include identification of ncRNAs that could be potential therapeutic targets in endocrine-resistant tumors, as well as ncRNA biomarkers that facilitate more tumor-specific treatment options for endocrine-resistant breast cancer patients.
引用
收藏
页数:13
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