Lin Zhexuan, Zhang Quanwei, Luo Wenhong
The Key Lab of Molecular Biology for High Cancer Incidence Coastal Chaoshan Area, Shantou University Medical College, Shantou 515041, Guangdong, China.
The Key Lab of Molecular Biology for High Cancer Incidence Coastal Chaoshan Area, Shantou University Medical College, Shantou 515041, Guangdong, China.
Eur J Pharmacol. 2016 Dec 15;793:76-81. doi: 10.1016/j.ejphar.2016.10.039. Epub 2016 Nov 11.
Angiogenesis has become an attractive target for cancer therapy since the US Food and Drug Administration (FDA) approved the first angiogenesis inhibitor (bevacizumab) for the treatment of metastatic colorectal cancer in 2004. In following years, a large number of angiogenesis inhibitors have been discovered and developed, ranging from monoclonal antibodies, endogenous peptides, to small organic molecules and microRNAs. Many of them are now entering the clinical trial, or achieving approval for clinical use. However, major limitations have been observed about angiogenesis inhibitors by continued clinical investigations, such as resistance, enhancing tumor hypoxia and reducing delivery of chemotherapeutic agents, which might be the main reason for poor improvement in overall survival after angiogenesis inhibitor administration in clinic. Therefore, optimal anti-angiogenic therapy strategies become critical. The present review summarizes recent researches in angiogenesis inhibitors, and proposes a perspective on future directions in this field.
自2004年美国食品药品监督管理局(FDA)批准首款血管生成抑制剂(贝伐单抗)用于治疗转移性结直肠癌以来,血管生成已成为癌症治疗中一个颇具吸引力的靶点。在随后的几年里,大量的血管生成抑制剂被发现和开发出来,从单克隆抗体、内源性肽到小分子有机化合物和微小RNA。它们中的许多目前正进入临床试验阶段,或已获批临床使用。然而,持续的临床研究发现血管生成抑制剂存在一些主要局限性,如耐药性、加剧肿瘤缺氧以及减少化疗药物的递送,这可能是临床上使用血管生成抑制剂后总体生存率改善不佳的主要原因。因此,最佳的抗血管生成治疗策略变得至关重要。本综述总结了血管生成抑制剂的最新研究,并对该领域的未来发展方向提出了展望。