Li Tongtong, Shen Xuan, Zhang Tao, Ren Jiaheng, Wang Wang, Wang Didi, Zhang Pengxia
Key Laboratory of Microecology-Immune Regulatory Network and Related Diseases School of Basic Medicine, Jiamusi University, Jiamusi, Heilongjiang, China.
Department of Basic Medicine, Jiangsu Medical College, Yancheng, Jiangsu, China.
J Clin Transl Hepatol. 2025 Jun 28;13(6):469-483. doi: 10.14218/JCTH.2024.00369. Epub 2025 Apr 18.
Hepatocellular carcinoma (HCC) remains challenging to treat in advanced stages, primarily due to the development of resistance to sorafenib. There is an urgent need for novel therapeutic strategies to overcome this resistance. This study aimed to investigate the potential of oleanolic acid (OA), a natural hepatoprotective compound, in mitigating sorafenib resistance and elucidate its underlying molecular mechanisms.
Sorafenib-resistant Huh7 and HepG2 cell lines were established to mimic the resistant phenotype. The effects of OA on these cells were evaluated by assessing cell invasion, migration, and sensitivity to sorafenib. Gene expression analysis was conducted to identify molecular changes induced by OA treatment, with a focus on expression.
Oleanolic acid significantly inhibited the invasive and migratory capabilities of sorafenib-resistant Huh7 and HepG2 cells ( < 0.01). Furthermore, OA treatment downregulated expression and restored the cells' sensitivity to sorafenib.
Oleanolic acid shows promise as an adjunct therapy for overcoming sorafenib resistance in HCC. By reducing cell aggressiveness and restoring drug sensitivity, OA may enhance the therapeutic efficacy of current treatments for advanced HCC.
肝细胞癌(HCC)晚期治疗仍具有挑战性,主要原因是对索拉非尼产生耐药性。迫切需要新的治疗策略来克服这种耐药性。本研究旨在探讨天然保肝化合物齐墩果酸(OA)在减轻索拉非尼耐药性方面的潜力,并阐明其潜在的分子机制。
建立索拉非尼耐药的Huh7和HepG2细胞系以模拟耐药表型。通过评估细胞侵袭、迁移和对索拉非尼的敏感性来评价OA对这些细胞的作用。进行基因表达分析以鉴定OA处理诱导的分子变化,重点关注[此处原文缺失相关基因名称]表达。
齐墩果酸显著抑制索拉非尼耐药的Huh7和HepG2细胞的侵袭和迁移能力(<0.01)。此外,OA处理下调了[此处原文缺失相关基因名称]表达并恢复了细胞对索拉非尼的敏感性。
齐墩果酸有望作为克服HCC中索拉非尼耐药性的辅助治疗方法。通过降低细胞侵袭性和恢复药物敏感性,OA可能提高晚期HCC当前治疗的疗效。