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基于索拉非尼的联合分子靶向治疗肝细胞癌

Sorafenib-based combined molecule targeting in treatment of hepatocellular carcinoma.

作者信息

Gao Jian-Jun, Shi Zhen-Yan, Xia Ju-Feng, Inagaki Yoshinori, Tang Wei

机构信息

Jian-Jun Gao, Zhen-Yan Shi, Department of Pharmacology, School of Pharmaceutical Sciences, Qingdao University, Qingdao 266021, Shandong Province, China.

出版信息

World J Gastroenterol. 2015 Nov 14;21(42):12059-70. doi: 10.3748/wjg.v21.i42.12059.

Abstract

Sorafenib is the only and standard systematic chemotherapy drug for treatment of advanced hepatocellular carcinoma (HCC) at the current stage. Although sorafenib showed survival benefits in large randomized phase III studies, its clinical benefits remain modest and most often consist of temporary tumor stabilization, indicating that more effective first-line treatment regimens or second-line salvage therapies are required. The molecular pathogenesis of HCC is very complex, involving hyperactivated signal transduction pathways such as RAS/RAF/MEK/ERK and PI3K/AKT/mTOR and aberrant expression of molecules such as receptor tyrosine kinases and histone deacetylases. Simultaneous or sequential abrogation of these critical pathways or the functions of these key molecules involved in angiogenesis, proliferation, and apoptosis may yield major improvements in the management of HCC. In this review, we summarize the emerging sorafenib-based combined molecule targeting for HCC treatment and analyze the rationales of these combinations.

摘要

索拉非尼是现阶段治疗晚期肝细胞癌(HCC)唯一的标准系统化疗药物。尽管索拉非尼在大型随机III期研究中显示出对生存期有益,但它的临床获益仍然有限,且大多只是暂时稳定肿瘤,这表明需要更有效的一线治疗方案或二线挽救疗法。HCC的分子发病机制非常复杂,涉及RAS/RAF/MEK/ERK和PI3K/AKT/mTOR等过度激活的信号转导通路以及受体酪氨酸激酶和组蛋白脱乙酰酶等分子的异常表达。同时或序贯阻断这些关键通路或参与血管生成、增殖和凋亡的这些关键分子的功能,可能会在HCC的治疗管理方面取得重大进展。在本综述中,我们总结了新兴的以索拉非尼为基础的联合分子靶向治疗HCC的方法,并分析了这些联合治疗的理论依据。

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