Unraveling the Molecular Mechanisms Involved in HCV-Induced Carcinogenesis.
Tania Guadalupe Heredia-TorresAna Rosa Rincón-SánchezSonia Amelia Lozano-SepúlvedaKame Alberto Galan-HuertaDaniel Arellanos-SotoMarisela García-HernándezAurora de Jesús Garza-JuarezAna María Guadalupe Rivas-EstillaPublished in: Viruses (2022)
Cancer induced by a viral infection is among the leading causes of cancer. Hepatitis C Virus (HCV) is a hepatotropic oncogenic positive-sense RNA virus that leads to chronic infection, exposing the liver to a continuous process of damage and regeneration and promoting hepatocarcinogenesis. The virus promotes the development of carcinogenesis through indirect and direct molecular mechanisms such as chronic inflammation, oxidative stress, steatosis, genetic alterations, epithelial-mesenchymal transition, proliferation, and apoptosis, among others. Recently, direct-acting antivirals (DAAs) showed sustained virologic response in 95% of cases. Nevertheless, patients treated with DAAs have reported an unexpected increase in the early incidence of Hepatocellular carcinoma (HCC). Studies suggest that HCV induces epigenetic regulation through non-coding RNAs, DNA methylation, and chromatin remodeling, which modify gene expressions and induce genomic instability related to HCC development that persists with the infection's clearance. The need for a better understanding of the molecular mechanisms associated with the development of carcinogenesis is evident. The aim of this review was to unravel the molecular pathways involved in the development of carcinogenesis before, during, and after the viral infection's resolution, and how these pathways were regulated by the virus, to find control points that can be used as potential therapeutic targets.
Keyphrases
- hepatitis c virus
- oxidative stress
- dna methylation
- epithelial mesenchymal transition
- genome wide
- human immunodeficiency virus
- diabetic rats
- papillary thyroid
- dna damage
- signaling pathway
- drug induced
- hiv infected
- risk factors
- squamous cell carcinoma
- ischemia reperfusion injury
- induced apoptosis
- high glucose
- cell proliferation
- squamous cell
- metabolic syndrome
- antiretroviral therapy
- risk assessment
- cell cycle arrest
- case control