Pro-apoptotic and anti-proliferative activities of cassane diterpenoids on squamous carcinoma cells: An in vitro and in silico study.

Q1 Environmental Science Toxicology Reports Pub Date : 2024-11-29 eCollection Date: 2024-12-01 DOI:10.1016/j.toxrep.2024.101833
Kelly Oriakhi, Osayemwenre Erharuyi, Kissinger O Orumwensodia, Emmanuel E Essien, Abiodun Falodun, Patrick O Uadia, Frerich Bernhard, Nadja Engel
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Abstract

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 Caesalpinia pulcherrima cassane diterpenoids on squamous carcinoma cells in vitro. 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.

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cassane二萜对鳞状癌细胞的促凋亡和抗增殖活性:体外和硅细胞研究。
头颈部鳞状癌的特点是异常凋亡,延长细胞的增殖能力和不受控制的细胞生长。本研究旨在探讨山参二萜对鳞癌细胞的促凋亡和抗增殖作用。我们测定了从紫皮蕉中分离的4种cassane二萜{6 -cinnamoyl- 7- hydroxychaapen -5-ol(1)、pulcherrimin A(2)、C(3)和E(4)}在鳞状癌细胞系(CAL33、FaDu和Detroit 562)和非致瘤性成纤维细胞中的细胞毒性。结果表明,化合物1和4具有最高的细胞毒潜能,在所有鳞状细胞系中显著降低细胞活力,并呈浓度依赖性。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CAL33细胞的增殖。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受体的结合亲和力较强,分别为-8.5和-8.8 kcal/mol。这些结果表明,Pulcherrimin E和6-肉桂酰-7-羟基戊二烯-5-醇在体外对鳞状癌细胞具有选择性细胞毒作用,具有潜在的抗肿瘤作用。
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来源期刊
Toxicology Reports
Toxicology Reports Environmental Science-Health, Toxicology and Mutagenesis
CiteScore
7.60
自引率
0.00%
发文量
228
审稿时长
11 weeks
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