小RNA
生物
乳腺癌
计算生物学
抑制器
基因表达调控
基因
上皮-间质转换
癌症
生物信息学
癌症研究
遗传学
转移
作者
Jaganathan Venkatesh,Marie‐Claire D. Wasson,Justin M. Brown,Wasundara Fernando,Paola Marcato
出处
期刊:Cancer Letters
[Elsevier BV]
日期:2021-04-16
卷期号:509: 81-88
被引量:120
标识
DOI:10.1016/j.canlet.2021.04.002
摘要
Therapeutic effectiveness in breast cancer can be limited by the underlying mechanisms of pathogenesis, including epithelial-mesenchymal transition (EMT), cancer stem cells (CSCs) and drug resistance. Long non-coding RNAs (lncRNAs) and microRNAs (miRNAs) are master regulators of gene expression and are functionally important mediators in these mechanisms of pathogenesis. Intricate crosstalks between these non-coding RNAs form complex regulatory networks of post-transcriptional gene regulation. Depending on the specific lncRNA/miRNA interaction, the lncRNA-miRNA axis can have tumor suppressor or oncogenic effects, thus defining the lncRNA-miRNA axis is important for determining targetability. Herein, we summarize the current literature describing lncRNA-miRNA interactions that are critical in the molecular mechanisms that regulate EMT, CSCs and drug resistance in breast cancer. Further, we review both the well-studied and potential novel mechanisms of lncRNA-miRNA interactions in breast cancer.
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