Anticancer effects of punicalagin and 5-fluorouracil on laryngeal squamous cell carcinoma: an in vitro study

Amany M. Taha, Eman Abd-Elshafy, Asmaa M. Khalifa, N. Dar-Odeh, Shadia Elsayed, Daniah S. Alharkan, Aishah Alhodhodi, Ahmed Saaduddin Sapri, Yassmeen SalahEldin Ragheb, G. Balbola
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Abstract

The purpose of this study was to assess the apoptotic effects of punicalagin alone and in combination with 5-fluorouracil (5-FU) on laryngeal squamous cell carcinoma (Hep-2) cell line. Hep-2 cells were cultured and divided into four groups: Group 1 received no therapy and served as control, Group 2 received 5-FU only, Group 3 received punicalagin only, and Group 4 received a combination of 5-FU and punicalagin. After 48 hours of incubation, cellular changes were examined under an inverted microscope. The methyl thiazolyl tetrazolium assay, caspase-3 gene level, and vascular endothelial growth factor (VEGF) level were assessed. The control group showed the highest mean value of cancer cell proliferation rate (1.595±0.58), followed by the punicalagin group (1.263±0.447), then the 5-FU group (0.827±0.256), while the combination group showed the lowest proliferation rate (0.253±0.111). The combination group showed the highest mean value of caspase-3 concentration (3.177±0.736), followed by the 5-FU group (1.830±0.646), and punicalagin group (0.741±0.302), while the control group showed the lowest mean value (0.359±0.117). Regarding VEGF levels, the control group had a statistically significant higher mean value, followed by the punicalagin and 5-FU groups, and finally, the combination group which showed the lowest value. Punicalagin exerts an anticancer effect through anti-proliferative action and induction of apoptosis on Hep-2 cell line. Combining punicalagin with 5-FU potentiates its anti-proliferative, apoptotic, and anti-angiogenic actions. It, further, helps in mitigating the putative side effects of 5-FU by reducing the dose required for its therapeutic effects.
潘尼卡星和 5-氟尿嘧啶对喉鳞状细胞癌的抗癌作用:体外研究
本研究的目的是评估孔雀石绿单独或与 5-氟尿嘧啶(5-FU)联合使用对喉鳞癌(Hep-2)细胞株的凋亡作用。Hep-2 细胞经培养后分为四组:第 1 组不接受治疗,作为对照组;第 2 组只接受 5-FU;第 3 组只接受 punicalagin;第 4 组接受 5-FU 和 punicalagin 混合治疗。培养 48 小时后,在倒置显微镜下观察细胞变化。评估甲基噻唑基四氮唑试验、Caspase-3 基因水平和血管内皮生长因子(VEGF)水平。结果显示,对照组的癌细胞增殖率平均值最高(1.595±0.58),其次是扑尔敏组(1.263±0.447),然后是 5-FU 组(0.827±0.256),而联合组的癌细胞增殖率最低(0.253±0.111)。Caspase-3浓度的平均值以联合组最高(3.177±0.736),其次是5-FU组(1.830±0.646)和punicalagin组(0.741±0.302),而对照组的平均值最低(0.359±0.117)。在血管内皮生长因子水平方面,对照组的平均值较高,具有显著的统计学意义,其次是Punicalagin组和5-FU组,最后是联合组,其平均值最低。Punicalagin 通过抗增殖作用和诱导 Hep-2 细胞凋亡发挥抗癌作用。将 Punicalagin 与 5-FU 结合使用可增强其抗增殖、凋亡和抗血管生成作用。此外,它还有助于减轻 5-FU 的副作用,降低其治疗效果所需的剂量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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