Significance of Methylation of FBP1 Gene in Non-Small Cell Lung Cancer.
Yao DongSheng HuayingWan DanyingZhu ChihongJiang RuibinSun XiaojiangJianguo FengPublished in: BioMed research international (2018)
Because NSCLC has poor overall prognosis and is frequently diagnosed at later stage, we aimed to seek novel diagnosis biomarkers or therapy target of the disease in this study. Fructose-1,6-bisphosphatase 1 (FBP1) is a rate-limiting enzyme in gluconeogenesis, which was usually lost in NSCLC due to abnormal methylation in promoter DNA sequence. The clinical data indicated that the methylation rate in FBP1 gene promoter was negatively related to the overall survival of the NSCLC patients. DNA methylation transferase inhibitor 5-aza treatment could significantly increase both expression levels of mRNA and protein in A549 cell line. On the other hand, silence of FBP1 in H460 cell line by using specific siRNA against FBP1 dramatically improved the cell proliferation and cell migration according to the date of FACS and transwell assays. All these findings implied the important roles of FBP1 expression in lung cancer development and progression and the potential use of the methylation status detected in FBP1 promoter region as a novel predictor for prognosis and therapeutic target for NSCLC patients.
Keyphrases
- dna methylation
- genome wide
- small cell lung cancer
- end stage renal disease
- gene expression
- ejection fraction
- newly diagnosed
- cell proliferation
- poor prognosis
- advanced non small cell lung cancer
- chronic kidney disease
- cell migration
- prognostic factors
- peritoneal dialysis
- transcription factor
- binding protein
- high throughput
- risk assessment
- drug delivery
- single molecule
- long non coding rna
- big data
- deep learning
- cell free
- combination therapy
- genome wide identification
- free survival