Department of Pathology, Beth Israel Deaconess Medical Center and Harvard Medical School, The Center for Vascular Biology Research, 99 Brookline Ave, Boston, MA 02215, United States.
Semin Cancer Biol. 2022 Nov;86(Pt 2):126-135. doi: 10.1016/j.semcancer.2022.09.006. Epub 2022 Sep 30.
Considerable progress has been made in our understanding of the process of angiogenesis in the context of normal and tumor tissue over the last fifty years. Angiogenesis, like most physiological processes, is carefully controlled by dynamic and opposing effects of positive factors, such as vascular endothelial growth factor (VEGF), and negative factors, such as thrombospondin-1. In most cases, the progression of a small mass of cancerous cells to a life-threatening tumor depends upon the initiation of angiogenesis and involves the dysregulation of the angiogenic balance. Whereas our newfound appreciation for the role of angiogenesis in cancer has opened up new avenues for treatment, the success of these treatments, which have focused almost exclusively on antagonizing the VEGF pathway, has been limited to date. It is anticipated that this situation will improve as more therapeutics that target other pathways are developed, more strategies for combination therapies are advanced, more detailed stratification of patient populations occurs, and a better understanding of resistance to anti-angiogenic therapy is gained.
在过去的五十年中,我们对正常组织和肿瘤组织中血管生成过程的理解取得了很大的进展。血管生成,像大多数生理过程一样,受到正性因素(如血管内皮生长因子 [VEGF])和负性因素(如血栓调节蛋白-1)的动态和拮抗作用的精细调控。在大多数情况下,一小部分癌细胞发展为危及生命的肿瘤取决于血管生成的启动,并涉及血管生成平衡的失调。尽管我们对血管生成在癌症中的作用有了新的认识,为治疗开辟了新的途径,但到目前为止,这些治疗方法的成功(几乎完全集中在拮抗 VEGF 途径上)是有限的。随着针对其他途径的治疗方法的开发、联合治疗策略的推进、对患者人群的更详细分层以及对血管生成抑制治疗耐药性的更好理解,预计这种情况将会改善。