BACKGROUND: Curcumin, a bioactive compound derived from Curcuma longa, has gained attention for its potential therapeutic effects in liver cancer. We reviewed current literature to evaluate the efficacy of curcumin in liver cancer models, such as anti-proliferative, pro-apoptotic, anti-inflammatory, or anti-metastatic roles. This systematic review focused on experimental methods, dosages, and underlying mechanisms. METHODS: A comprehensive literature search was conducted across PubMed, Web of Science, Embase, and Google Scholar until December 2024. Inclusion criteria were studies using in vivo or in vitro models to assess curcumin's effects on liver cancer, with comparisons to control groups. A total of 26 studies (8 in vivo, 14 in vitro, 4 combined) were included. Data on curcumin administration methods, dosages, and outcomes were extracted. Study quality was assessed using a six-item scale. Descriptive statistics were used for data analysis with SPSS (Version 22.0). RESULTS: From the initial 1048 studies retrieved, 27 met the inclusion criteria. In vivo studies were conducted on various animals strains (C3H/HeN mice, Wistar rats, B6C3F1 mice, BALB/c nude mice and C57BL/6 mice). Curcumin was administered via oral (8 studies), intraperitoneal (2 studies), intragastric (1 study) and intravenous (1 study) routes, with 8 studies incorporating a dose gradient. The majority of studies used chemically-induced models, including N-diethylnitrosamine (DEN) and nitrosodiethylamine (NDEA) models, as well as subcutaneous injections of liver cancer cell lines (HepG2, Bel7402). The included studies employed various techniques, including Western blotting, RT-PCR, flow cytometry, and migration assays. Curcumin significantly induced apoptosis in liver cancer cells, with 14 studies reporting dose-dependent increases in apoptosis markers such as caspase-3 and Bax expression. Anti-inflammatory effects were evident in 5 studies, with curcumin inhibiting NF-κB activation, a key pathway in liver cancer progression. Additionally, antioxidant and anti-angiogenic properties were observed, as curcumin reduced lipid peroxidation and decreased VEGF expression. Two studies highlighted curcumin's potential in suppressing metastasis, with dose-dependent inhibition of liver cancer cell migration and invasion. The quality of included studies varied, with 21 out of 27 studies employing random allocation and 8 using blinded outcome assessments. CONCLUSIONS: Curcumin demonstrates promising anti-cancer effects, including apoptosis induction, inflammation modulation, and metastasis inhibition. However, variability in study designs and lack of clinical trials necessitate standardized protocols and further clinical investigations to confirm its therapeutic potential in liver cancer treatment.