蜂胶对PPP2R1A及癌细胞凋亡的影响

IF 3.4 Q2 BIOCHEMICAL RESEARCH METHODS
Biochemistry Research International Pub Date : 2025-01-15 eCollection Date: 2025-01-01 DOI:10.1155/bri/5538068
Burak Durmaz, Latife Merve Oktay Çelebi, Ayşe Çekin, Ayshan Ahadova, Nur Selvi Günel, Hatice Kalkan Yıldırım, Ali Mert Özgönül, Eser Yıldırım Sözmen
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引用次数: 0

摘要

最近,研究表明蛋白磷酸酶2A (PP2A)功能障碍在许多癌症类型中都很常见,并通过多种失活机制介导。虽然许多研究发现蜂胶提取物对各种类型的癌症具有抗肿瘤作用,但其作用机制尚不清楚。本研究以健康成纤维细胞WI-38为对照,研究蜂胶对SW-620(结直肠癌)、DU-145和PC-3(前列腺癌)和MCF-7(乳腺癌)细胞系PPP2R1A表达的影响及其与凋亡的关系。此外,我们旨在通过分析肿瘤坏死因子相关凋亡诱导配体(TRAIL)、APAF-1和caspase -3、-8和-9等凋亡标志物来研究蜂胶对细胞凋亡的影响。提取蜂胶样品,采用LC-MS/MS对其酚类化合物进行定量分析。采用实时细胞分析系统- xcelligence (RTCA-SP)设备和软件评估蜂胶样品的细胞活力和细胞毒性。测定蜂胶的IC50值(SW-620 298 μg/mL, DU-145 185.6 μg/mL, PC -3 250.7 μg/mL, MCF-7 292.9 μg/mL, WI-38 311.2 μg/mL)。随后,分析蜂胶对PPP2R1A表达和凋亡标志物(TRAIL、Apaf-1、caspase -3、-8和-9)的影响。当我们将健康细胞系与癌细胞细胞系进行比较时,在SW-620细胞系中,应用蜂胶后观察到caspase-3(3.62倍)和TRAIL(4.38倍)的增加具有统计学意义。此外,在PC-3细胞系中,caspase-8与健康细胞系相比增加了1.4倍,也具有统计学意义。我们的研究结果表明,蜂胶增加了癌细胞PPP2R1A水平和凋亡标志物。有研究表明,蜂胶处理引起的PPP2R1A水平升高可能激活了细胞凋亡途径。本研究首次证实了蜂胶对PPP2R1A水平的诱导作用,而PPP2R1A被认为是癌症治疗的新靶点。研究结果表明,蜂胶通过增加PPP2R1A水平,有望成为一种潜在的癌症治疗药物,PPP2R1A是癌症治疗的关键分子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of Propolis on PPP2R1A and Apoptosis in Cancer Cells.

Recently, it has been shown that protein phosphatase 2A (PP2A) dysfunction was common in many cancer types and was mediated by various inactivation mechanisms. Although many research studies observed antitumor effect of propolis extracts in various types of cancer, the mechanism of effect are still obscure. In this study, we investigated the effect of propolis on PPP2R1A expression and its relationship with apoptosis in the SW-620 (colorectal cancer), DU-145 and PC-3 (prostate cancer), and MCF-7 (breast cancer) cell lines, with WI-38 (healthy fibroblast) cells serving as the control. Moreover, we aimed to investigate the impact of propolis on apoptosis by analyzing apoptosis markers such as tumor necrosis factor-related apoptosis-inducing ligand (TRAIL), APAF-1, and caspases-3, -8, and -9. Propolis samples were extracted, and their phenolic compounds were quantified using LC-MS/MS. The RealTime Cell Analysis System-xCELLigence (RTCA-SP) device and software were employed to assess cell viability and cytotoxicity of the propolis samples. The IC50 values for propolis were determined (298 μg/mL for SW-620, 185.6 μg/mL for DU-145, 250.7 μg/mL for PC - 3, 292.9 μg/mL for MCF-7, and 311.2 μg/mL for WI-38). Subsequently, the effects of propolis on PPP2R1A expression and apoptosis markers (TRAIL, Apaf-1, and caspases-3, -8, and -9) were analyzed. When we compared the healthy cell lines to cancer cell lines, a statistically significant increase in caspase-3 (3.62-fold) and in TRAIL (4.38-fold) was observed in the SW-620 cell line after the application of propolis. In addition, in the PC-3 cell line, a 1.4-fold increase in caspase-8 was observed compared with the healthy cell line, which is also statistically significant. Our findings indicated that propolis increased the PPP2R1A levels and apoptosis markers in cancer cell lines. It has been suggested that high PPP2R1A levels induced by propolis treatment might activate the apoptosis pathway. In this study, the inducible effect of propolis on PPP2R1A levels, identified as a new target for cancer treatment, was demonstrated for the first time. The findings suggest that propolis holds promise as a potential cancer therapy by increasing PPP2R1A levels, a key molecule in cancer treatment.

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来源期刊
Biochemistry Research International
Biochemistry Research International BIOCHEMICAL RESEARCH METHODS-
CiteScore
6.30
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0.00%
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27
审稿时长
14 weeks
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