Insulin-Like Growth Factor Binding Protein 5-A Probable Target of Kidney Renal Papillary Renal Cell Carcinoma.
Shuqiang WangQuan HongXiaodong GengKun ChiGuangyan CaiDi WuPublished in: BioMed research international (2019)
Kidney renal papillary renal cell carcinoma (KIRP) accounts for 10-15% of renal cell carcinoma (RCC). The need to find more therapeutic targets for KIRP is urgent because most targeted drugs have limited effects on advanced KIRP. Insulin-like growth factor (IGF) binding protein 5 (IGFBP5) is a secreted protein related to cell proliferation, cell adhesion, cell migration, the inflammatory response and fibrosis; these functions are independent of IGF. In our study, we determined the expression and functions of IGFBP5 with data from the database of The Cancer Genome Atlas (TCGA). We found that IGFBP5 is down regulated in KIRP kidney tissues compared to its expression in control tissues and that the expression of IGFBP5 is negatively related to patient survival. Bioinformatic analysis showed the probable processes and pathways involved in altered IGFBP5 expression, including blood vessel development, the cellular response to growth factor stimulus, the response to transforming growth factor β (TGF-β), and extracellular matrix organization. We proposed that VEGFA and TGF-β act as upstream regulatory factors of IGFBP5 and verified this in the Caki-2 cell line. Based on our results, we suggest that IGFBP5 might be a therapeutic target of KIRP.
Keyphrases
- binding protein
- renal cell carcinoma
- transforming growth factor
- poor prognosis
- growth factor
- cell migration
- extracellular matrix
- cell proliferation
- inflammatory response
- epithelial mesenchymal transition
- gene expression
- transcription factor
- cell adhesion
- long non coding rna
- squamous cell carcinoma
- emergency department
- machine learning
- drug delivery
- growth hormone
- electronic health record
- papillary thyroid
- protein protein
- genome wide
- young adults
- childhood cancer
- free survival