Tofigh Pouya, Mirghazanfari Seyed Mehdi, Hami Zahra, Nassireslami Ehsan, Ebrahimi Mohsen
Toxicology Research Center, AJA University of Medical Sciences, Tehran, Iran.
Department of Physiology, School of Medicine, AJA University of Medical Sciences, Tehran, Iran.
Rep Biochem Mol Biol. 2024 Jan;12(4):596-608. doi: 10.61186/rbmb.12.4.596.
The therapeutic potential of Quercus infectoria (QI) gall, including its anti-inflammatory, antioxidant, and anticancer properties, is well-known. However, its impact on lung, gastric, and esophageal cancer cells remain unclear. This study aims to explore the effects of QI gall aqueous extract on cell viability, apoptosis, and gene expression in A549, BGC823, and KYSE-30 cell lines.
A549, BGC823, and KYSE-30 cells were seeded in complete medium and incubated with different concentrations of QI gall extract for 24 hours. Cell viability was measured by an MTT [3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyl tetrazolium bromide] assay. The induction of apoptosis was assessed through flow cytometric analysis after the adding FITC-conjugated Annexin V (Annexin V-FITC) and propidium iodide (PI). The mRNA expression levels of , , and genes were determined using Real-time Quantitative Polymerase Chain Reaction analysis.
The MTT assay demonstrated that treatment with QI gall extract significantly reduced the number of viable cells in the A549, BGC823, and KYSE-30 cell lines at IC50 concentrations of 440.1, 437.1, and 465.2 mg/ml, respectively. Additionally, compared to untreated cell population, the percentages of early apoptosis, late apoptosis, and necrosis in the A549, BGC823, and KYSE-30 cells significantly increased following treatment with QI gall extract (P< 0.05). Also, the treatment with QI gall extract influenced the expression of , , and genes.
The present findings indicated that the gall extract of QI can inhibit the growth of A549, BGC823, and KYSE-30 cells by inducing apoptosis, which may be mediated via mitochondria-dependent pathway.
没食子(QI)五倍子的治疗潜力,包括其抗炎、抗氧化和抗癌特性,是众所周知的。然而,其对肺癌、胃癌和食管癌细胞的影响仍不清楚。本研究旨在探讨没食子五倍子水提取物对A549、BGC823和KYSE - 30细胞系细胞活力、凋亡和基因表达的影响。
将A549、BGC823和KYSE - 30细胞接种于完全培养基中,并用不同浓度的没食子五倍子提取物孵育24小时。通过MTT [3 -(4,5 - 二甲基噻唑 - 2 - 基)- 2,5 - 二苯基溴化四氮唑] 试验测量细胞活力。加入异硫氰酸荧光素(FITC)偶联的膜联蛋白V(膜联蛋白V - FITC)和碘化丙啶(PI)后,通过流式细胞术分析评估凋亡诱导情况。使用实时定量聚合酶链反应分析测定 、 、 和 基因的mRNA表达水平。
MTT试验表明,没食子五倍子提取物处理在IC50浓度分别为440.1、437.1和465.2 mg/ml时,显著降低了A549、BGC823和KYSE - 30细胞系中的活细胞数量。此外,与未处理的细胞群体相比,没食子五倍子提取物处理后,A549、BGC823和KYSE - 30细胞中的早期凋亡、晚期凋亡和坏死百分比显著增加(P < 0.05)。而且,没食子五倍子提取物处理影响了 、 、 和 基因的表达。
目前的研究结果表明,没食子五倍子的五倍子提取物可通过诱导凋亡抑制A549、BGC823和KYSE - 30细胞的生长,这可能通过线粒体依赖性途径介导。