肝细胞癌
医学
转移
新生血管
血管生成
索拉非尼
血管性
癌症研究
肿瘤科
靶向治疗
舒尼替尼
内科学
病理
癌症
作者
Shinji Tanaka,Shigeki Arii
标识
DOI:10.1053/j.seminoncol.2012.05.005
摘要
In vivo tumor progression requires the supply of oxygen and nutrition by neovasculature. Hepatocellular carcinoma (HCC) is one of the typical tumors with neovascularization, and the dramatic alteration in the arterial vascularity may lead to acquisition of the potential for vascular invasiveness and metastasis. In 2008, phase III clinical trials revealed anti-angiogenic agent "sorafenib" as the first drug that demonstrated an improved overall survival in patients with advanced HCC. A new era of HCC treatment had arrived, but there has been limited further improvement in survival benefits. This review summarizes molecular targeted therapy with a focus on angiogenesis, growth signals, and mitotic abnormalities, as well as the promising concepts of "cancer stemness" and "synthetic lethality" for the strategy of targeted therapy.
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