Rankin Erinn B, Giaccia Amato J
Division of Radiation and Cancer Biology, Department of Radiation Oncology, Stanford University Medical Center, Stanford, CA 94305-5152, USA. Department of Obstetrics and Gynecology, Stanford University Medical Center, Stanford, CA 94305-5152, USA.
Division of Radiation and Cancer Biology, Department of Radiation Oncology, Stanford University Medical Center, Stanford, CA 94305-5152, USA.
Science. 2016 Apr 8;352(6282):175-80. doi: 10.1126/science.aaf4405. Epub 2016 Apr 7.
Metastatic disease is the leading cause of cancer-related deaths and involves critical interactions between tumor cells and the microenvironment. Hypoxia is a potent microenvironmental factor promoting metastatic progression. Clinically, hypoxia and the expression of the hypoxia-inducible transcription factors HIF-1 and HIF-2 are associated with increased distant metastasis and poor survival in a variety of tumor types. Moreover, HIF signaling in malignant cells influences multiple steps within the metastatic cascade. Here we review research focused on elucidating the mechanisms by which the hypoxic tumor microenvironment promotes metastatic progression. These studies have identified potential biomarkers and therapeutic targets regulated by hypoxia that could be incorporated into strategies aimed at preventing and treating metastatic disease.
转移性疾病是癌症相关死亡的主要原因,涉及肿瘤细胞与微环境之间的关键相互作用。缺氧是促进转移进展的一种强大的微环境因素。在临床上,缺氧以及缺氧诱导转录因子HIF-1和HIF-2的表达与多种肿瘤类型中远处转移增加和生存率低相关。此外,恶性细胞中的HIF信号传导影响转移级联反应中的多个步骤。在此,我们综述了旨在阐明缺氧肿瘤微环境促进转移进展机制的研究。这些研究已经确定了受缺氧调节的潜在生物标志物和治疗靶点,可将其纳入旨在预防和治疗转移性疾病的策略中。