Published online May 26, 2022. doi: 10.12998/wjcc.v10.i15.4737
Peer-review started: September 13, 2021
First decision: January 23, 2022
Revised: February 2, 2022
Accepted: April 2, 2022
Article in press: April 2, 2022
Published online: May 26, 2022
Processing time: 253 Days and 0.9 Hours
Metabolic reprogramming is a feature of tumour cells and is essential to support their rapid proliferation. Lipid metabolism reprogramming enables tumour cells to meet their needs for highly proliferative growth and is an important driving force for the development of hepatocellular carcinoma (HCC).
We explored the influence of different metabolic subtypes of HCC and analysed their significance in guiding prognosis and treatment based on the molecular mechanism of glycolysis and fatty acid oxidation (FAO).
To explore the influence of different metabolic subtypes of HCC and analyse their significance in guiding prognosis and treatment.
We utilised unsupervised consensus clustering to divide the Cancer Genome Atlas-liver hepatocellular carcinoma samples into four metabolic subgroups and compared single nucleotide polymorphism, copy number variation, tumour microenvironment, and Genomics of Drug Sensitivity in Cancer and Tumour Immune Dysfunction and Exclusion between different metabolites. In addition, we established a prognostic model based on glycolysis and FAO genes.
We established a prognostic model and found that the fatty acid oxidation group and the low-risk group had better efficacy and response to immune checkpoint blockade treatment and anti-tumour drugs.
There are obvious differences in genes, chromosomes, and clinical characteristics between metabolic subgroups.
The establishment of a prognostic model could predict patient prognosis and guide clinical treatment.
