Vascular endothelial growth factor A is a potential prognostic biomarker and correlates with immune cell infiltration in hepatocellular carcinoma.
Yuchen QiYinghui SongMengting CaiJianwen LiZhangtao YuYuhang LiJunkai HuangYu JiangChuang PengBo JiangSulai LiuPublished in: Journal of cellular and molecular medicine (2023)
Hepatocellular carcinoma (HCC) is the fourth leading cause of cancer-related deaths among cancer patients. Vascular endothelial growth factor A (VEGFA) is involved in regulating biological processes, such as angiogenesis and vascular permeability, and is very closely related to the pathogenesis of various tumours, especially vascular-rich, solid tumours. Clinical data of patients with HCC and other tumours were analysed through public databases, such as the TCGA database, Gene Expression Omnibus database, Human Protein Atlas database, STRING, Tumour Immune Estimation Resource and Kaplan-Meier Plotter. The tumour tissues and adjacent normal tissues of patients with HCC from Hunan Provincial People's Hospital were collected to verify the expression of VEGFA by immunohistochemistry, immunofluorescence, Western blotting and qPCR. VEGFA expression is elevated in multiple tumour types and correlates with the prognosis of tumour patients. VEGFA is involved in regulating the tumour microenvironment and immune cell function in tumour development. Inhibition of VEGFA reduces proliferation, invasion, and migration and promotes apoptosis in HCC cells. VEGFA is a potential predictive biomarker for the diagnosis and prognosis of HCC.
Keyphrases
- vascular endothelial growth factor
- endothelial cells
- gene expression
- poor prognosis
- adverse drug
- cell cycle arrest
- healthcare
- newly diagnosed
- end stage renal disease
- stem cells
- oxidative stress
- binding protein
- induced apoptosis
- ejection fraction
- mental health
- cell death
- chronic kidney disease
- emergency department
- south africa
- prognostic factors
- electronic health record
- cell proliferation
- induced pluripotent stem cells
- patient reported outcomes
- patient reported