Qadir Abdul, Samad Danish Abdus, Asif Mahayrookh, Ali Muhammad Mujtaba, Zain Syeda
Department of Pharmacology, United Medical and Dental College, Karachi, Pakistan.
Department of Surgery, Fatima Jinnah Dental College, Karachi, Pakistan.
J Taibah Univ Med Sci. 2023 Mar 8;18(5):1011-1017. doi: 10.1016/j.jtumed.2023.02.016. eCollection 2023 Oct.
Angiogenesis plays an important role in various physiological and pathological conditions and is essential for tumor growth and metastasis. The aim of this study was to evaluate the effect of a combination of vandetanib and celecoxib on angiogenic tube formation and its effect on angiogenic genes (MMP-2 and MMP-9) using an model of human umbilical vein endothelial cells (HUVECs).
HUVECs were cultured and verified by flow cytometry. HUVECs were then treated with vandetanib, celecoxib, and the combination of both drugs. Then, we investigated cell viability and cell apoptosis by MTT assays and flow cytometry. The process of angiogenesis was analyzed by tube formation assays, and the effect on angiogenic genes was determined by RT-qPCR.
HUVECs were positive for CD144 and negative for CD14. Vandetanib, celecoxib, and their combination inhibited HUVEC viability in a dose-dependent manner (p < 0.001). The rate of apoptosis was 13.1%, 9%, and 23.7% (p < 0.001) when treated with vandetanib, celecoxib, or the combination of both drugs, respectively. Vandetanib inhibited tube formation by 43.7%, celecoxib by 21%, and their combination by 77.3% (p < 0.001), respectively. RT-qPCR revealed that both vandetanib and celecoxib reduced the expression levels of MMP-2 and MMP-9, and their combination resulted in an even greater extent of reduction in expression levels (p < 0.001).
Celecoxib enhanced the effect of vandetanib in inhibiting angiogenesis and the combination of these two drugs led to even greater extents of inhibition than vandetanib alone.
血管生成在各种生理和病理状况中发挥重要作用,对肿瘤生长和转移至关重要。本研究旨在使用人脐静脉内皮细胞(HUVECs)模型评估凡德他尼与塞来昔布联合用药对血管生成管形成的影响及其对血管生成基因(MMP - 2和MMP - 9)的作用。
培养HUVECs并通过流式细胞术进行验证。然后用凡德他尼、塞来昔布以及两种药物的联合制剂处理HUVECs。接着,通过MTT法和流式细胞术研究细胞活力和细胞凋亡。通过管形成试验分析血管生成过程,并通过RT - qPCR确定对血管生成基因的作用。
HUVECs对CD144呈阳性,对CD14呈阴性。凡德他尼、塞来昔布及其联合制剂以剂量依赖方式抑制HUVEC活力(p < 0.001)。分别用凡德他尼、塞来昔布或两种药物联合处理时,细胞凋亡率分别为13.1%、9%和23.7%(p < 0.001)。凡德他尼、塞来昔布及其联合制剂分别使管形成抑制43.7%、21%和77.3%(p < 0.001)。RT - qPCR显示凡德他尼和塞来昔布均降低MMP - 2和MMP - 9的表达水平,且两者联合导致表达水平降低幅度更大(p < 0.001)。
塞来昔布增强了凡德他尼抑制血管生成的作用,且这两种药物联合使用比单独使用凡德他尼导致更大程度的抑制。