Carcinoma hepatocelular en Perú: una descripción molecular de un cuadro clínico atípico

• Autores: Contreras-Mancilla, J, Cerapio, JP, Ruiz, E, Fernández, R, Casavilca-Zambrano, S, Machicado, C, Fournié, JJ, Pineau, P, Bertani, S
• Formato: artículo
• Fecha de Publicación: 2024
• Institución: Instituto Nacional de Enfermedades Neoplásicas
• Repositorio: INEN-Institucional
• Lenguaje: inglés
• OAI Identifier: oai:repositorio.inen.sld.pe:20.500.14703/387
• Enlace del recurso: https: //doi.org/10.1016/j.rgmx.2023.01.003; https://hdl.handle.net/20.500.14703/387
• Nivel de acceso: acceso abierto
• Materia: DNA methylation; Hepatocellular carcinoma; Peru; Transcriptome; https://purl.org/pe-repo/ocde/ford#3.02.21

Introduction: Hepatocellular carcinoma (HCC) is the third most frequent cancer of digestive tract tumors in Peru, with a high mortality rate of 17.7 per 100,000 inhabitants. A significant number of HCC cases in Peru do not follow the classic clinical epidemiology of the disease described in other parts of the world. Those patients present with a distinct transcriptome profile and a singular tumor process, suggesting a particular type of hepatocarcinogenesis in a portion of the Peruvian population. Aim: Our aim was to understand the clinical and biologic involvement of the epigenetic profile (methylation) and gene expression (transcriptome) of HCC in Peruvian patients. Methods: HCC and liver transcriptome and DNA methylation profiles were evaluated in 74 Peruvian patients. Results: When grouped by age, there was greater DNA methylation in younger patients with HCC but no differences with respect to the transcriptomic profile. A high prevalence of the hepatitis B virus (HBV) (> 90%) was also observed in the younger patients with HCC. Enrichment analyses in both molecular profiles pinpointed PRC2 as an important molecular effector of that liver tumor process in Peruvian patients. Conclusion: HCC in Peruvian patients has a unique molecular profile, associated with the presence of HBV, as well as overall DNA hypermethylation related to undifferentiated liver cells or cellular reprogramming.