Department of Pathology, School of Medicine, University of Phayao, Thailand.
Unit of Excellence of Pharmacological Research on Medicinal Plants, University of Phayao, Thailand.
Asian Pac J Cancer Prev. 2024 May 1;25(5):1579-1587. doi: 10.31557/APJCP.2024.25.5.1579.
Gac aril contains high level of carotenoids. This carotenoid possesses several pharmacological properties including antioxidant, anti-inflammatory, and anti-tumor activities.
To investigate the anti-cancer activity of Gac aril extract on human colorectal cancer cells and its related mechanisms.
Colorectal cancer cell lines HCT116 and HT29 were treated with Gac aril extract and its effects on cytotoxicity and anti-proliferation were analyzed using the MTT/MTS and colony formation assay, respectively. Then, further related mechanisms responsible for anti-proliferation were investigated by cell death detection ELISA and Flow cytometry.
The results showed that treated cells became rounded up and there was a loss of contact with neighboring cells, leading to a reduction of cell viability. The cytotoxic effects were evaluated IC50 for HCT116 and HT29 cells were 2.16 mg/mL and 1.29 mg/mL, respectively but it not toxic to normal HEK293 at the same dose. Moreover, Gac aril extract significantly inhibits proliferative ability with increasing concentrations having a greater effect. Subsequently, the cellular mechanism responsible for suppressive proliferation was validated. It shows apoptosis induction and arrest of cell cycle.
Our findings demonstrated that Gac aril extract can induce apoptosis and arrest of cell cycle at S and G2/M phases in both HCT116 and HT29 colorectal cancer cells.
余甘果含有高水平的类胡萝卜素。这种类胡萝卜素具有多种药理特性,包括抗氧化、抗炎和抗肿瘤活性。
研究余甘果提取物对人结肠癌细胞的抗癌活性及其相关机制。
用余甘果提取物处理结肠癌细胞系 HCT116 和 HT29,分别用 MTT/MTS 和集落形成试验分析其对细胞毒性和抗增殖的影响。然后,通过细胞死亡检测 ELISA 和流式细胞术进一步研究与增殖抑制相关的机制。
结果表明,处理后的细胞变圆,与相邻细胞失去接触,导致细胞活力降低。对 HCT116 和 HT29 细胞的细胞毒性作用的 IC50 值分别为 2.16mg/mL 和 1.29mg/mL,但在相同剂量下对正常 HEK293 细胞没有毒性。此外,余甘果提取物显著抑制增殖能力,浓度增加的效果更大。随后,验证了抑制增殖的细胞机制。结果表明诱导细胞凋亡和细胞周期停滞在 S 和 G2/M 期。
我们的研究结果表明,余甘果提取物可以诱导 HCT116 和 HT29 结肠癌细胞凋亡和细胞周期停滞在 S 和 G2/M 期。