The Circadian Rhythm Gene Arntl2 Is a Metastasis Susceptibility Gene for Estrogen Receptor-Negative Breast Cancer.
Ngoc-Han HaJirong LongQiuyin CaiXiao Ou ShuKent W HunterPublished in: PLoS genetics (2016)
Breast cancer mortality is primarily due to metastasis rather than primary tumors, yet relatively little is understood regarding the etiology of metastatic breast cancer. Previously, using a mouse genetics approach, we demonstrated that inherited germline polymorphisms contribute to metastatic disease, and that these single nucleotide polymorphisms (SNPs) could be used to predict outcome in breast cancer patients. In this study, a backcross between a highly metastatic (FVB/NJ) and low metastatic (MOLF/EiJ) mouse strain identified Arntl2, a gene encoding a circadian rhythm transcription factor, as a metastasis susceptibility gene associated with progression, specifically in estrogen receptor-negative breast cancer patients. Integrated whole genome sequence analysis with DNase hypersensitivity sites reveals SNPs in the predicted promoter of Arntl2. Using CRISPR/Cas9-mediated substitution of the MOLF promoter, we demonstrate that the SNPs regulate Arntl2 transcription and affect metastatic burden. Finally, analysis of SNPs associated with ARNTL2 expression in human breast cancer patients revealed reproducible associations of ARNTL2 expression quantitative trait loci (eQTL) SNPs with disease-free survival, consistent with the mouse studies.
Keyphrases
- genome wide
- estrogen receptor
- dna methylation
- transcription factor
- copy number
- squamous cell carcinoma
- small cell lung cancer
- crispr cas
- genome wide identification
- poor prognosis
- free survival
- gene expression
- metastatic breast cancer
- endothelial cells
- cardiovascular disease
- type diabetes
- genome editing
- dna repair
- heart rate
- coronary artery disease
- mass spectrometry
- binding protein
- dna binding
- dna damage