Authors
Leticia Cardoso Valente, Julia Stocco da Silva, Luana Riechelmann-Casarin, Fernando Gomes Romeiro, Luís Fernando Barbisan, Guilherme Ribeiro Romualdo
Published in
Journal of biochemical and molecular toxicology. Volume 40. Issue 7. Pages e71017.
Abstract
Hepatocellular carcinoma (HCC) features a high mortality burden worldwide, highlighting the need for improved therapeutic strategies. Caffeine (CAF), a widely consumed bioactive compound, has been reported to exert chemopreventive effects in HCC, but its interaction with standard therapies remains poorly explored. We investigated whether CAF enhances the antitumor effects of sorafenib (SOR) chemotherapy in preclinical HCC models. C3H/HeJ mice were submitted to diethylnitrosamine (DEN)-induced hepatocarcinogenesis and treated with CAF (50 mg/kg), SOR (30 mg/kg), or their combination for 3 weeks. C3A+LX2 spheroids and transwell co-cultures were also exposed to CAF, SOR, or their combination at 1/5 or 1/10 of the half-maximal effective concentration. The combination of CAF and SOR produced a synergistic reduction in tumor spheroid viability, consistent with the transcriptomic alterations observed, and inhibited HCC cell colony formation. Nonetheless, treatments exerted comparable effects on reducing liver tumor volume and Afp expression in vivo. Although only CAF + SOR reduced serum ALT levels and uniquely downregulated HCC-related Ccl3, treatments showed differential and subtle transcriptomic impacts in DEN-induced hepatocarcinogenesis, with no promoting or additive effects when combined. In summary, while CAF potentiated SOR antitumoral activity in vitro, their combination did not lead to major effects in vivo, eliciting the need for further investigation.
PMID:
42455914
Bibliographic data and abstract were imported from PubMed on 16 Jul 2026.
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