Department of Pharmacognosy, "Victor Babeș" University of Medicine and Pharmacy Timișoara, Romania, Eftimie Murgu Sq. No. 2, 300041 Timișoara, Romania.
Research Center for Pharmaco-Toxicological Evaluation, "Victor Babeș" University of Medicine and Pharmacy Timișoara, Romania, Eftimie Murgu Sq. No. 2, 300041 Timișoara, Romania.
Anal Cell Pathol (Amst). 2021 Jun 21;2021:5552664. doi: 10.1155/2021/5552664. eCollection 2021.
One of the most important class of natural compounds with successful preclinical results in the management of cancer is the flavonoids. Due to the plethora of biological activities, apigenin (4',5,7 trihydroxyflavone) is a main representant of the flavone subclass. Although the antiproliferative and antiangiogenic effects of apigenin were studied on a significant number of human and murine melanoma cell lines, in order to complete the data existing in the literature, the aim of this study is to evaluate the effect of apigenin on SK-MEL-24 human melanoma cell line as well as on tumor angiogenesis using the aforementioned cell line on the chorioallantoic membrane assay. Results have shown that in the range of tested doses, the phytocompound presents significant antiproliferative, cytotoxic, and antimigratory potential at 30 M, respectively, 60 M. Moreover, the phytocompound in both tested concentrations limited melanoma cell growth and migration and induced a reduced angiogenic reaction limiting melanoma cell development.
具有成功的临床前结果的最重要的一类天然化合物之一是类黄酮。由于具有丰富的生物活性,芹菜素(4',5,7-三羟基黄酮)是黄酮类化合物的主要代表。尽管已经在大量的人和鼠黑色素瘤细胞系上研究了芹菜素的抗增殖和抗血管生成作用,但为了完善文献中现有的数据,本研究旨在评估芹菜素对 SK-MEL-24 人黑色素瘤细胞系的作用,以及使用上述细胞系在鸡胚尿囊膜试验中对肿瘤血管生成的作用。结果表明,在测试剂量范围内,该植物化合物在 30μM 时分别表现出显著的抗增殖、细胞毒性和抗迁移潜力,在 60μM 时也表现出显著的抗增殖、细胞毒性和抗迁移潜力。此外,该植物化合物在两种测试浓度下均限制了黑色素瘤细胞的生长和迁移,并诱导了减少的血管生成反应,从而限制了黑色素瘤细胞的发展。