Medical Oncology, National Center for Tumor Diseases (NCT), University of Heidelberg and German Cancer Research Center (DKFZ), Im Neuenheimer Feld 460, 69120 Heidelberg, Germany.
J Oncol. 2012;2012:281261. doi: 10.1155/2012/281261. Epub 2011 Aug 24.
Tumorigenesis is a complex multistep process involving not only genetic and epigenetic changes in the tumor cell but also selective supportive conditions of the deregulated tumor microenvironment. One key compartment of the microenvironment is the vascular niche. The role of angiogenesis in solid tumors but also in hematologic malignancies is now well established. Research on angiogenesis in general, and vascular endothelial growth factor in particular, is a major focus in biomedicine and has led to the clinical approval of several antiangiogenic agents including thalidomide, bevacizumab, sorafenib, sunitinib, pazopanib, temesirolimus, and everolimus. Indeed, antiangiogenic agents have significantly changed treatment strategies in solid tumors (colorectal cancer, renal cell carcinoma, and breast cancer) and multiple myeloma. Here we illustrate important aspects in the interrelationship between tumor cells and the microenvironment leading to tumor progression, with focus on angiogenesis, and summarize derived targeted therapies.
肿瘤发生是一个复杂的多步骤过程,不仅涉及肿瘤细胞中的遗传和表观遗传改变,还涉及失调的肿瘤微环境的选择性支持条件。微环境的一个关键部分是血管壁龛。血管生成在实体瘤中的作用,以及在血液恶性肿瘤中的作用,现在已经得到充分证实。关于血管生成的研究,特别是血管内皮生长因子的研究,是生物医学的一个主要重点,并导致了几种抗血管生成药物的临床批准,包括沙利度胺、贝伐珠单抗、索拉非尼、舒尼替尼、帕唑帕尼、替西罗莫司和依维莫司。事实上,抗血管生成药物已经显著改变了实体瘤(结直肠癌、肾细胞癌和乳腺癌)和多发性骨髓瘤的治疗策略。在这里,我们将说明导致肿瘤进展的肿瘤细胞与微环境之间相互关系的重要方面,重点是血管生成,并总结衍生的靶向治疗。