Al-Abd Ahmed M, Alamoudi Abdulmohsin J, Abdel-Naim Ashraf B, Neamatallah Thikryat A, Ashour Osama M
Pharmacology Department, Medical Division, National Research Centre, Dokki, Giza, Egypt.
Department of Pharmacology and Toxicology, Faculty of Pharmacy, King Abdulaziz University, Jeddah, Saudi Arabia.
J Adv Res. 2017 Nov;8(6):591-605. doi: 10.1016/j.jare.2017.06.006. Epub 2017 Jun 27.
Recent strategies for the treatment of cancer, other than just tumor cell killing have been under intensive development, such as anti-angiogenic therapeutic approach. Angiogenesis inhibition is an important strategy for the treatment of solid tumors, which basically depends on cutting off the blood supply to tumor micro-regions, resulting in pan-hypoxia and pan-necrosis within solid tumor tissues. The differential activation of angiogenesis between normal and tumor tissues makes this process an attractive strategic target for anti-tumor drug discovery. The principles of anti-angiogenic treatment for solid tumors were originally proposed in 1972, and ever since, it has become a putative target for therapies directed against solid tumors. In the early twenty first century, the FDA approved anti-angiogenic drugs, such as bevacizumab and sorafenib for the treatment of several solid tumors. Over the past two decades, researches have continued to improve the performance of anti-angiogenic drugs, describe their drug interaction potential, and uncover possible reasons for potential treatment resistance. Herein, we present an update to the pre-clinical and clinical situations of anti-angiogenic agents and discuss the most recent trends in this field.
除了单纯杀死肿瘤细胞外,近期针对癌症的治疗策略一直在深入研发中,比如抗血管生成治疗方法。血管生成抑制是实体瘤治疗的一项重要策略,其基本原理是切断肿瘤微区域的血液供应,导致实体瘤组织内广泛缺氧和坏死。正常组织与肿瘤组织之间血管生成的差异激活,使得这一过程成为抗肿瘤药物研发中一个有吸引力的战略靶点。实体瘤抗血管生成治疗的原理最初于1972年提出,从那时起,它就成为了针对实体瘤治疗的一个假定靶点。在21世纪初,美国食品药品监督管理局(FDA)批准了抗血管生成药物,如贝伐单抗和索拉非尼用于治疗多种实体瘤。在过去的二十年里,研究人员不断改进抗血管生成药物的性能,描述它们的药物相互作用潜力,并揭示潜在治疗耐药性的可能原因。在此,我们介绍抗血管生成药物临床前和临床情况的最新进展,并讨论该领域的最新趋势。