Dysregulation of miRNAs-COUP-TFII-FOXM1-CENPF axis contributes to the metastasis of prostate cancer.
Shih-Chieh LinChung-Yang KaoHui-Ju LeeChad J CreightonMichael M IttmannShaw-Jeng TsaiSophia Y TsaiMing-Jer TsaiPublished in: Nature communications (2016)
Although early detection and treatment of prostate cancer (PCa) improves outcomes, many patients still die of metastatic PCa. Here, we report that metastatic PCa exhibits reduced levels of the microRNAsmiR-101 and miR-27a. These micro-RNAs (miRNAs) negatively regulate cell invasion and inhibit the expression of FOXM1 and CENPF, two master regulators of metastasis in PCa. Interestingly, the repression of FOXM1 and CENPF by these miRNAs occurs through COUP-TFII, a member of the orphan nuclear receptors family. Loss of miR-101 positively correlates with the increase of COUP-TFII-FOXM1-CENPF activity in clinical PCa data sets, implicating clinical relevance of such regulation. Further studies show that COUP-TFII is a critical factor controlling metastatic gene networks to promote PCa metastasis. Most importantly, this miRNA-COUP-TFII-FOXM1-CENPF regulatory axis is also involved in the development of enzalutaminde resistance. Taken together, our findings highlight the contribution of specific miRNAs through the regulation of the COUP-TFII-FOXM1-CENPF cascade in PCa metastasis and drug resistance.
Keyphrases
- prostate cancer
- squamous cell carcinoma
- small cell lung cancer
- cell proliferation
- long non coding rna
- end stage renal disease
- radical prostatectomy
- poor prognosis
- newly diagnosed
- chronic kidney disease
- transcription factor
- ejection fraction
- long noncoding rna
- gene expression
- adipose tissue
- copy number
- peritoneal dialysis
- dna methylation
- electronic health record
- insulin resistance
- data analysis
- genome wide identification