Kang Rui, Song Mengdi, Fang Zhou, Liu Kehai
Department of Biopharmaceutics, College of Food Science and Technology, Shanghai Ocean University, Shanghai, PR China.
J Drug Target. 2023 Feb;31(2):166-178. doi: 10.1080/1061186X.2022.2115047. Epub 2022 Aug 31.
Vasculogenic mimicry (VM) describes the phenomenon whereby fluid-conducting vessels are formed by highly invasive tumour cells, which supply blood to tumours during their early growth stages. Single antiangiogenic agents have limited inhibitory effects on VM, therefore, a multi-pathway anti-VM strategy is required. In this study, Apatinib (Apa) was coordinated with Cu to form a Cu-Apa copper complex. The latter was loaded into oligo-hyaluronic acid (HA) polymeric micelles (HA-Chol) and subsequently embedded in polysaccharide-based in situ hydrogels (APsGels) to generate Cu-Apa/HA-Chol@APsGels. In this system, Cu-Apa exerts the combined effects of Cu and Apa to inhibit VM; HA-Chol micelles achieve targeted drug delivery and enhance endocytosis efficiency; APsGels realise sustained release of the drugs to ensure an anti-VM effect. This system demonstrated improved VM inhibition with low cytotoxicity and high biocompatibility, wound healing, and transwell invasion in three-dimensional cell cultured VM. Moreover, this system significantly inhibited VM formation and melanoma growth in a mouse tumour transplantation model. This study provides an effective strategy for inhibiting VM.
血管生成拟态(VM)描述了一种现象,即由高侵袭性肿瘤细胞形成流体传导血管,这些血管在肿瘤早期生长阶段为其供血。单一抗血管生成药物对VM的抑制作用有限,因此,需要一种多途径抗VM策略。在本研究中,阿帕替尼(Apa)与铜配位形成铜-阿帕替尼铜络合物。将后者负载到寡聚透明质酸(HA)聚合物胶束(HA-Chol)中,随后嵌入多糖基原位水凝胶(APsGels)中,以生成铜-阿帕替尼/HA-Chol@APsGels。在该体系中,铜-阿帕替尼发挥铜和阿帕替尼的联合作用来抑制VM;HA-Chol胶束实现靶向药物递送并提高内吞效率;APsGels实现药物的持续释放以确保抗VM效果。该体系在三维细胞培养的VM中表现出增强的VM抑制作用,具有低细胞毒性和高生物相容性、促进伤口愈合以及抑制穿膜侵袭。此外,该体系在小鼠肿瘤移植模型中显著抑制VM形成和黑色素瘤生长。本研究为抑制VM提供了一种有效策略。