Gacche R N, Meshram R J, Shegokar H D, Gond D S, Kamble S S, Dhabadge V N, Utage B G, Patil K K, More R A
School of Life Sciences, Swami Ramanand Teerth Marathwada University, Nanded 431 606, MS, India.
School of Life Sciences, Swami Ramanand Teerth Marathwada University, Nanded 431 606, MS, India.
Arch Biochem Biophys. 2015 Jul;577-578:35-48. doi: 10.1016/j.abb.2015.04.009. Epub 2015 Apr 30.
Relationship between structural diversity and biological activities of flavonoids has remained an important discourse in the mainstream of flavonoid research. In the current study anti-angiogenic, cytotoxic, antioxidant and cyclooxygenase (COX) inhibitory activities of diverse class of flavonoids including hydroxyl and methoxy substituted flavones, flavonones and flavonols have been evaluated in the light of developing flavonoids as a potential scaffold for designing novel anti-antiangiogenic agents. We demonstrate anti-angiogenic potential of flavonoids using in vivo chorioallantoic membrane model (CAM) and further elaborate the possible structural reasoning behind observed anti-angiogenic effect using in silico methods. Additionally, we report antioxidant potential and kinetics of free radical scavenging activity using DPPH and SOR scavenging assays. Current study indicates that selected flavonoids possess considerable COX inhibition potential. Furthermore, we describe cytotoxicity of flavonoids against selected cancer cell lines using MTT cell viability assay. Structural analysis of in silico docking poses and predicted binding free energy values are not only in accordance with the experimental anti-angiogenic CAM values from this study but also are in agreement with the previously reported literature on crystallographic data concerning EGFR and VEGFR inhibition.
黄酮类化合物的结构多样性与生物活性之间的关系一直是黄酮类研究主流中的一个重要话题。在当前的研究中,鉴于将黄酮类化合物开发为设计新型抗血管生成剂的潜在支架,对包括羟基和甲氧基取代的黄酮、黄酮醇和黄酮醇在内的多种黄酮类化合物的抗血管生成、细胞毒性、抗氧化和环氧化酶(COX)抑制活性进行了评估。我们使用体内鸡胚绒毛尿囊膜模型(CAM)证明了黄酮类化合物的抗血管生成潜力,并使用计算机模拟方法进一步阐述了观察到的抗血管生成作用背后可能的结构原因。此外,我们使用DPPH和SOR清除试验报告了抗氧化潜力和自由基清除活性的动力学。当前的研究表明,所选的黄酮类化合物具有相当大的COX抑制潜力。此外,我们使用MTT细胞活力试验描述了黄酮类化合物对所选癌细胞系的细胞毒性。计算机模拟对接构象的结构分析和预测的结合自由能值不仅与本研究的实验性抗血管生成CAM值一致,而且与先前报道的关于EGFR和VEGFR抑制的晶体学数据的文献一致。