Department of Hematology and Medical Oncology, Cleveland Clinic Taussig Cancer Institute, 9500 Euclid Avenue, Desk CA60, Cleveland, OH, 44195, USA.
Curr Oncol Rep. 2019 Jan 22;21(1):6. doi: 10.1007/s11912-019-0752-z.
In this review, the importance of the hypoxia inducible factor (HIF) pathway in tumorigenesis and cancer treatment outcomes will be discussed. The outcomes of phase II and III clinical trials of direct HIF inhibitors in the treatment of cancer will be reviewed.
The HIF signaling pathway is activated by tumor-induced hypoxia or by inactivating mutations of the VHL gene. HIF is a transcription factor which regulates the expression of genes involved in adjusting mechanisms to hypoxia such as angiogenesis or apoptosis as well as tumor growth, invasion, and metastasis. The HIF pathway has a key role in development of resistance to different treatment modalities and higher expression of the HIF molecule is associated with poor prognosis. Clinical studies of the HIF inhibitors in patients with advanced/refractory cancers suggest benefit and warrant further studies of the HIF inhibitors either as a single agent or in combination with other therapeutic agents.
在这篇综述中,将讨论缺氧诱导因子(HIF)通路在肿瘤发生和癌症治疗结果中的重要性。将回顾直接 HIF 抑制剂治疗癌症的 II 期和 III 期临床试验结果。
HIF 信号通路被肿瘤诱导的缺氧或 VHL 基因突变失活所激活。HIF 是一种转录因子,它调节参与缺氧适应机制的基因的表达,如血管生成或凋亡以及肿瘤生长、侵袭和转移。HIF 通路在对不同治疗方式的耐药性发展中起关键作用,HIF 分子的高表达与预后不良相关。在晚期/难治性癌症患者中进行的 HIF 抑制剂的临床研究表明了获益,这使得进一步研究 HIF 抑制剂作为单一药物或与其他治疗药物联合使用成为必要。