C1R suppresses hepatocellular carcinoma cell aggressiveness through promoting HIF-1α degradation and modulating cuproptosis-related protein expression.
TL;DR
A model in which C1R reduces aggressive phenotypes of HCC cells partly through destabilizing HIF-1α and reshaping copper-responsive processes is supported, which supports a model in which C1R reduces aggressive phenotypes of HCC cells partly through destabilizing HIF-1α and reshaping copper-responsive processes.
Abstract
Background
Hepatocellular carcinoma (HCC) frequently develops in the setting of chronic hepatitis B virus (HBV) infection, yet the molecular events shared by HBV-related liver injury and malignant transformation remain incompletely characterized. Recent studies of cuproptosis indicate that copper overload can disturb mitochondrial metabolic programs in tumor cells. This rationale prompted us to examine copper-responsive alterations across chronic HBV-related liver injury and HCC.
Methods
TCGA-LIHC and GSE230397 datasets were analyzed to identify shared differentially expressed genes between HCC and chronic HBV infection. Functional enrichment, ssGSEA, WGCNA, and five machine-learning algorithms were used to screen cuproptosis-associated candidate genes. C1R expression, prognosis, immune infiltration, and immune checkpoint correlations were assessed. Experimental validation was then performed in HCC cell lines by manipulating C1R expression and assessing copper modulation, HIF-1α rescue, intracellular localization, protein expression, oxidative stress, cell motility, HIF-1α stability, proteasome inhibition, and ubiquitination.
Results
The integrated analysis identified 423 genes with concordant dysregulation in the HBV and HCC datasets. These genes were linked to metal ion response, oxidative stress, and copper-associated biological processes. Cuproptosis-related scores were lower in both HCC tissues and HBV-infected liver samples. Integrative WGCNA and machine-learning analyses identified C1R as the only shared cuproptosis associated candidate gene. C1R was downregulated in HCC and associated with survival, immune infiltration, and immune checkpoint molecules. Functionally, C1R overexpression increased FDX1, DLAT, and DLST expression, elevated ROS accumulation, and suppressed HCC cell migration and invasion, whereas C1R knockdown produced opposite effects. Copper chelation with TTM weakened the effects of C1R overexpression, whereas combined elesclomol and CuCl₂ treatment intensified the C1R-associated changes. C1R also lowered HIF-1α levels by the proteasome-sensitive process accompanied by increased HIF-1α ubiquitination. Restoring HIF-1α expression counteracted the effects of C1R on FDX1, DLAT, DLST, invasion, and migration.
Conclusions
C1R is a shared cuproptosis-associated regulator in HBV infection and HCC. The data support a model in which C1R reduces aggressive phenotypes of HCC cells partly through destabilizing HIF-1α and reshaping copper-responsive processes.