Welsh Sarah J, Fife Kate
Cambridge University Hospitals NHS Foundation Trust, Cambridge, CB2 0QQ, UK.
Future Oncol. 2015;11(8):1169-79. doi: 10.2217/fon.14.274.
The incidence and mortality from renal cell cancer (RCC) is increasing. RCC tumors are particularly vascular in nature as a result of disruption of the VHL gene and/or its upstream pathway leading to upregulation of the hypoxia-inducible factor transcription factor. The hypoxia-inducible factor pathway drives angiogenesis by upregulating VEGF and bFGF, amongst other proangiogenic downstream target genes. Therapies which target angiogenesis have been successful in treating metastatic RCC (mRCC) and the receptor tyrosine kinase inhibitor, pazopanib, is licensed for first line treatment of mRCC. This review details the past, current and future roles of pazopanib in the treatment of mRCC.
肾细胞癌(RCC)的发病率和死亡率正在上升。由于VHL基因和/或其上游通路的破坏导致缺氧诱导因子转录因子上调,RCC肿瘤本质上具有特别丰富的血管。缺氧诱导因子通路通过上调VEGF和bFGF以及其他促血管生成的下游靶基因来驱动血管生成。靶向血管生成的疗法已成功用于治疗转移性肾细胞癌(mRCC),受体酪氨酸激酶抑制剂帕唑帕尼已被批准用于mRCC的一线治疗。本综述详细介绍了帕唑帕尼在mRCC治疗中的过去、现在和未来作用。