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叶绿醇对人非小细胞肺癌A549细胞的体外抗癌活性

In Vitro Anticancer Activity of Phytol on Human Non-Small Cell Lung Cancer A549 Cells.

作者信息

Yu Jie, Jin Feng, Tang Yingqi, Huang Yumin

机构信息

Department of Pulmonary and Critical Care Medicine, The Affiliated Hospital of Yangzhou University, Yangzhou University, Jiangsu, PR China.

Department of Pathology, Xinqiao Hospital, Army Medical University, Chongqing, China.

出版信息

Integr Cancer Ther. 2025 Jan-Dec;24:15347354251344592. doi: 10.1177/15347354251344592. Epub 2025 Jun 4.

Abstract

BACKGROUND

Non-small cell lung cancer (NSCLC) is the most common type of lung cancer. Many researchers have previously reported that natural compounds from plants or Chinese Traditional Herbs have a potential to treat NSCLC. But it has not been reported that phytol can treat NSCLC. In this research, we first exposed this effect on A549 cells and researched the mechanism.

METHODS

In order to evaluate whether phytol has a role in human NSCLC, a human non-tumoral bronchial epithelial cell line (NL20), adenocarcinomic human alveolar basal epithelial (A549) cell line, and NCI-H69 SCLC (H69) cell line were used for related experiments. After determining that phytol had no toxicity to NL20 cells, A549 cells, or H69 cells, the inhibitory effect of phytol on cancer cell related characteristics of cells were determined by luciferase assay, QRT-PCR, proliferation, invasion, and would healing cellular response experiments. Additionally, the quantification of apoptotic cells has been achieved through flow cytometry. Then, bioinformatics was used to establish a database to screen and speculate on phytol's corresponding targets in lung cancer. Finally, immunoblotting experiments were used to determine the specific pathways affected by phytol.

RESULTS

Treatment with phytol at concentrations ranging from 0 to 80 µM for 24 hours was not cytotoxic to the A549 cells and H69 cells. Phytol inhibited AP-1-mediated and NF-κB-mediated luciferase activity in a dose-dependent manner in A549 cells, but not H69 cells. Additionally, phytol significantly inhibited the levels of MMP9, IL-6, VEGFA, IL-8, and NFKBIA in A549 cells, but had no significant effects on H69 cells. Phytol induced significant dose-dependent growth inhibitory effects on A549 cells. A significant decrease in colony formation and migration was observed. Bioinformatic and immunoblotting analysis indicated that phytol inhibited proliferation and migration of A549 cells through the PI3K-Akt signaling pathway.

CONCLUSIONS

Phytol exhibits anticancer activity by inhibiting PI3K-Akt signaling pathway and may be applicable in the clinical prevention and treatment of lung cancer in the future.

摘要

背景

非小细胞肺癌(NSCLC)是最常见的肺癌类型。许多研究人员此前曾报道,来自植物或中药的天然化合物具有治疗NSCLC的潜力。但尚未有关于叶绿醇可治疗NSCLC的报道。在本研究中,我们首先揭示了其对A549细胞的这种作用并研究了其机制。

方法

为了评估叶绿醇在人类NSCLC中是否发挥作用,使用了一种人类非肿瘤性支气管上皮细胞系(NL20)、腺癌性人肺泡基底上皮(A549)细胞系和NCI-H69小细胞肺癌(H69)细胞系进行相关实验。在确定叶绿醇对NL20细胞、A549细胞或H69细胞无毒性后,通过荧光素酶测定、定量逆转录聚合酶链反应(QRT-PCR)、增殖、侵袭和伤口愈合细胞反应实验来确定叶绿醇对癌细胞相关细胞特性的抑制作用。此外,通过流式细胞术实现了凋亡细胞的定量分析。然后,利用生物信息学建立数据库以筛选和推测叶绿醇在肺癌中的相应靶点。最后,通过免疫印迹实验确定受叶绿醇影响的具体信号通路。

结果

用浓度范围为0至80μM的叶绿醇处理24小时对A549细胞和H69细胞无细胞毒性。叶绿醇在A549细胞中以剂量依赖性方式抑制AP-1介导和NF-κB介导的荧光素酶活性,但在H69细胞中无此作用。此外,叶绿醇显著抑制A549细胞中基质金属蛋白酶9(MMP9)、白细胞介素-6(IL-6)、血管内皮生长因子A(VEGFA)、白细胞介素-8(IL-8)和核因子κB抑制因子α(NFKBIA)的水平,但对H69细胞无显著影响。叶绿醇对A549细胞具有显著的剂量依赖性生长抑制作用。观察到集落形成和迁移显著减少。生物信息学和免疫印迹分析表明,叶绿醇通过PI3K-Akt信号通路抑制A549细胞的增殖和迁移。

结论

叶绿醇通过抑制PI3K-Akt信号通路表现出抗癌活性,未来可能适用于肺癌的临床防治。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a8/12141803/8fb542d596fd/10.1177_15347354251344592-fig2.jpg

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