4.4 Article

Identification of hub genes associated with obesity-induced hepatocellular carcinoma risk based on integrated bioinformatics analysis

Journal

MEDICAL ONCOLOGY
Volume 38, Issue 6, Pages -

Publisher

HUMANA PRESS INC
DOI: 10.1007/s12032-021-01510-0

Keywords

Obesity; Hepatocellular carcinoma; Bioinformatics analysis; Differentially expressed genes; Hub genes

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This study identified key genes (IGF1, ACADL, CYP2C9, and G6PD) involved in important metabolic pathways whose mRNA and protein expression levels are significantly altered in both obese individuals and patients with HCC, suggesting their potential as significant targets for the prevention and treatment of HCC development in obese individuals.
Obesity, which has become one of the biggest public health problems of the twenty-first century, accompanies many chronic conditions, including cancer. On the other hand, liver cancer, which is known to be associated with obesity, is considered another serious threat to public health. However, the underlying drivers of the development of obesity-associated hepatocellular carcinoma (HCC) remain blurry. The current study attempted to identify the key genes and pathways in the obesity-induced development of HCC using integrated bioinformatics analyses. Obesity and HCC-associated gene expression datasets were downloaded from Gene Expression Omnibus (GEO) and analyzed to identify overlapping differentially expressed genes (DEGs) and hub genes. The prognostic potentials, survival analysis, and expression levels of hub genes were further assessed. Moreover, the correlation between hub genes and the immune cells infiltration was analyzed. The findings of this research revealed that both mRNA and protein expression levels of the four hub genes (IGF1, ACADL, CYP2C9, and G6PD) involved in many important metabolic pathways are remarkably altered in both obese individuals and patients with HCC. The results demonstrated that these dysregulated genes in both obesity and HCC may serve as considerable targets for the prevention and treatment of HCC development in obese individuals.

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