Roberts Lewis R, Gores Gregory J
Division of Gastroenterology and Hepatology, Mayo Clinic College of Medicine, Rochester, Minnesota 55902, USA.
Semin Liver Dis. 2005;25(2):212-25. doi: 10.1055/s-2005-871200.
Hepatocellular carcinoma is often diagnosed at an advanced stage, when it is not amenable to curative therapies. There is no effective chemotherapy. Advances in cancer biology suggest that a limited number of pathways are responsible for initiating and maintaining dysregulated cell proliferation, which is the major cellular alteration responsible for the cancer phenotype. New treatments in development target several of these critical pathways, including agents targeting the receptor tyrosine kinase pathways, the Wnt/beta-catenin signaling pathway, the ubiquitin/proteasome degradation pathway, the epigenetic DNA methylation and histone deacetylation pathways, the PI3 kinase/AKT/mTOR pathway, angiogenic pathways, and telomerase. Several of these approaches hold significant promise for improving the long-term outcome of patients with advanced hepatocellular carcinoma. Because of the high prevalence of liver cirrhosis in hepatocellular carcinoma patients, these approaches must be coupled with new strategies for halting or reversing the progression of chronic liver disease.
肝细胞癌通常在晚期才被诊断出来,此时已无法进行根治性治疗。目前尚无有效的化疗方法。癌症生物学的进展表明,有限的几条信号通路负责启动和维持细胞增殖失调,而细胞增殖失调是导致癌症表型的主要细胞改变。正在研发的新疗法针对其中几条关键信号通路,包括靶向受体酪氨酸激酶通路、Wnt/β-连环蛋白信号通路、泛素/蛋白酶体降解通路、表观遗传DNA甲基化和组蛋白去乙酰化通路、PI3激酶/AKT/mTOR通路、血管生成通路以及端粒酶的药物。其中几种方法有望显著改善晚期肝细胞癌患者的长期预后。由于肝细胞癌患者中肝硬化的患病率很高,这些方法必须与阻止或逆转慢性肝病进展的新策略相结合。