Oriakhi Kelly, Erharuyi Osayemwenre, Orumwensodia Kissinger O, Essien Emmanuel E, Falodun Abiodun, Uadia Patrick O, Bernhard Frerich, Engel Nadja
Department of Medical Biochemistry, School of Basic Medical Sciences, College of Medical Sciences, University of Benin, Nigeria.
Department of Pharmaceutical Sciences, University of Kentucky, Lexington, USA.
Toxicol Rep. 2024 Nov 29;13:101833. doi: 10.1016/j.toxrep.2024.101833. eCollection 2024 Dec.
Squamous carcinoma of the head and neck is characterized by aberrant apoptosis that prolongs the proliferative capacity of the cells and by uncontrolled cell growth. This study aimed to examine the pro-apoptotic and antiproliferative effects of cassane diterpenoids on squamous carcinoma cells . The cytotoxicity of four (4) cassane diterpenoids {Six-cinnamoyl- 7-hydroxyvouacapen-5-ol(1), pulcherrimin A(2), C(3), and E(4)} isolated from C. pulcherrima was determined in squamous carcinoma cell lines (CAL33, FaDu, and Detroit 562) and in non tumorigenic fibroblast cells. The results showed that compounds 1 and 4 had the highest cytotoxic potential, significantly reducing cell viability in all squamous cell lines in a concentration dependent manner. Compounds 1 and 4 may inhibit the proliferation of CAL33 cells by reducing their ability to divide, decreasing PCNA expression, and suppressing migration. Additionally, treatment with compounds 1 and 4 led to an activation of Caspase 3 expression in FaDu cells. Molecular docking analysis revealed strong binding affinities of compounds 1 and 4 to the Caspase 3 receptor, with values of -8.5 and -8.8 kcal/mol, respectively. These results suggest that Pulcherrimin E and 6-cinnamoyl-7-hydroxylvouacapen-5-ol have potential antitumor effects based on their selective cytotoxic effect on squamous carcinoma cells in vitro.
头颈部鳞状细胞癌的特征在于异常凋亡,这种凋亡延长了细胞的增殖能力,并且细胞生长不受控制。本研究旨在研究决明二萜类化合物对鳞状癌细胞的促凋亡和抗增殖作用。从美丽决明中分离出的四种决明二萜类化合物{六肉桂酰基-7-羟基沃卡平-5-醇(1)、美丽决明素A(2)、C(3)和E(4)}的细胞毒性在鳞状癌细胞系(CAL33、FaDu和底特律562)和非致瘤性成纤维细胞中进行了测定。结果表明,化合物1和4具有最高的细胞毒性潜力,以浓度依赖性方式显著降低所有鳞状细胞系中的细胞活力。化合物1和4可能通过降低CAL33细胞的分裂能力、降低PCNA表达和抑制迁移来抑制其增殖。此外,用化合物1和4处理导致FaDu细胞中Caspase 3表达的激活。分子对接分析显示化合物1和4与Caspase 3受体具有很强的结合亲和力,其值分别为-8.5和-8.8 kcal/mol。这些结果表明,基于美丽决明素E和6-肉桂酰基-7-羟基沃卡平-5-醇在体外对鳞状癌细胞的选择性细胞毒性作用,它们具有潜在的抗肿瘤作用。