Journal de protéomique et bioinformatique
Libre accès
ISSN: 0974-276X
ISSN: 0974-276X
Jitendra Kumar, Purnima Tyagi, Raghwendra Pratap Singh, Akhilesh k Saini, Deepti Sharma, Jaswinder Singh Maras, Vijay Kumar
Background: Chronic Hepatitis B (CHB) infection and the Hepatitis B virus X protein (HBx) are major risk factors associated with Hepato Cellular Carcinoma (HCC). In CHB infection, HBx induces mitochondrial dysfunction, exhaustion and impaired function in hepatocytes. Restoring hepatocyte health along with reduction in virus replication could be an ideal treatment for CHB. Thiourea derivatives are well known for their antiviral properties, though their effect on mitochondrial and/or hepatocyte health remains obscure. This study focuses on the repurposing of thiourea derivatives (DSA-00, DSA-02 and DSA-09) for hepatocyte replenishment.
Methods: HepG2.2.15 cells were treated with thiourea derivatives, alongside Entecavir (ETV). HBV DNA, RNAs and antigens, measured by qPCR, Quantitative Reverse Transcriptase Polymerase Chain Reaction (RT-qPCR) and Enzyme-Linked Immunosorbent Assay (ELISA), respectively. Followed by proteomic analysis by Weighted Protein Co-expression Network Analysis (WPCNA) and Fluorescence Activated Cell Sorting (FACS) used for the validation of results.
Results: The proteomics analysis showed both DSA-00 and ETV were enriched with proteins associated with antiviral responses. In addition, DSA-00 additionally showed an increase in proteins linked to mitochondrial response. Whereas DSA-02 exhibited associations with the innate immune system and citric acid cycle and DSA-09 displayed pathways similar to DSA-00 and ETV. The treated groups exhibited an enhanced bio-energetic and antiviral response as compared to the untreated group. FACS analysis revealed the restoration of exhausted hepatocytes by thiourea derivatives through targeting mitochondria.
Conclusion: Our findings suggest that thiourea derivatives hold potential as a novel therapeutic agent that seems to restore mitochondrial health along with an anti-viral response in CHB.