FOLLOWUS
1.Department of Endocrinology and Metabolism, the First Hospital of Lanzhou University, Lanzhou (730000), China
2.Evidence Based Medicine Center, School of Basic Medical Science of Lanzhou University, Lanzhou (730000), China
3.Department of Computational Physics, Institute of Modern Physics, Chinese Academy of Sciences, Lanzhou (730000), China
4.School of Nuclear Science and Technology, University of Chinese Academy of Sciences, Beijing (100049), China
Dr. TIAN Yun-ling, E-mail: yunlingtian7318@126.com
纸质出版日期:2022-05-01,
网络出版日期:2021-09-21,
录用日期:2021-04-09
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Yun-ling TIAN, Song-bo FU, Bo LI, 等. 扶正抗癌方调节非小细胞肺癌肿瘤微环境研究[J]. Chinese Journal of Integrative Medicine, 2022,28(5):425-433.
Yun-ling TIAN, Song-bo FU, Bo LI, et al. Mechanism of Fuzheng Kang'ai Formula Regulating Tumor Microenvironment in Non-Small Cell Lung Cancer[J]. Chinese Journal of Integrative Medicine, 2022,28(5):425-433.
Yun-ling TIAN, Song-bo FU, Bo LI, 等. 扶正抗癌方调节非小细胞肺癌肿瘤微环境研究[J]. Chinese Journal of Integrative Medicine, 2022,28(5):425-433. DOI: 10.1007/s11655-021-3451-1.
Yun-ling TIAN, Song-bo FU, Bo LI, et al. Mechanism of Fuzheng Kang'ai Formula Regulating Tumor Microenvironment in Non-Small Cell Lung Cancer[J]. Chinese Journal of Integrative Medicine, 2022,28(5):425-433. DOI: 10.1007/s11655-021-3451-1.
目的:
2
研究中医药方剂扶正抗癌在肿瘤微环境中的调节机制.
方法:
2
本研究使用CIBERSORTx软件工具通过转录组数据分析肿瘤微环境. 中医药系统药学和分析平台 (TCMSP) 用于得到中医药成分和目标靶点的相互作用网络. 并使用癌症基因组图谱工具 (TCGA) 分析非小细胞肺癌与癌旁组织之间的差异基因. 此外
具有预后指示功能的差异基因通过单变量和多变量的Cox回归进行分析
与预后具有显著相关性的基因作为核心靶点. 使用扶正抗癌方的核心靶点结合肺腺癌肿瘤微环境进行相关性分析. 蛋白质相互作用数据库用于预测核心靶点下游基因
这些靶点是药物发挥作用的直接反应. 定量聚合酶链式反应的生物实验用于A549
H1299和PC9细胞系验证表达量
对于药物直接作用靶点以及靶点下游基因进行表达量的验证.
结果:
2
肿瘤微环境结果显示
活化的肥大细胞与非小细胞肺癌患者的预后具有显著性的关联(
P
<
0.05)
活化的肥大细胞分数高的显示预后越差. 在扶正抗癌方的靶点中
CCNA2是一个重要的的靶点 (风险率 (HR) =1.41
P
<
0.05) . CCNA2不仅是一个非小细胞肺癌的具有差异表达的预后基因
同时也与活化的肥大细胞具有显著的正相关性. CCNA2的下游基因包括BCL1L2、ACTL6A和ITGAV三个下游靶点
并通过A549验证这三个下游基因在扶正抗癌方的影响下表达变化情况.
结论:
2
扶正抗癌能够直接结合在CCNA2上并且通过调节下游基因来抑制肿瘤生长. 并且和肿瘤生长的相关肿瘤微环境紧密的与CCNA2相关.
Objective:
2
To study the mechanism of Chinese herbal medicine Fuzheng Kang'ai Formula (FZKA) on tumor microenvironment (TME).
Methods:
2
CIBERSORTx was used for analysis of TME. Traditional Chinese Medicine Systems Pharmacology and Analysis Platform was applied to identify compounds-targets network and the Cancer Genome Atlas (TCGA) was employed to identify the differential expression genes (DEGs) between tumor and paracancerous tissues in lung adenocarcinoma (LUAD) from TCGA-LUAD. Additionally
DEGs with prognosis in LUAD was calculated by univariable and multivariate Cox regression. The core targets of FZKA were analyzed in lung adenocarcinoma TME. Protein-protein interaction database was employed to predict down-stream of target. Quantitative reverse transcription polymerase chain reaction was employed for biological experiment in A549
H1299 and PC9 cell lines.
Results:
2
The active and resting mast cells were significantly associated with prognosis of LUAD (
P
<
0.05). Of the targets
CCNA2 as an important target of FZKA (hazard ratio=1.41
95% confidential interval: 1.01–2.01
P
<
0.05) was a prognostic target and significantly associated with mast cells. CCNA2 was positively correlated with mast cell activation and negatively correlated with mast cell resting state. BCL1L2
ACTL6A and ITGAV were down-stream of CCNA2
which were validated by qRT-PCR in A549 cell.
Conclusion:
2
FZKA could directly bind to CCNA2 and inhibit tumor growth by regulating CCNA2 downstream genes and TME of NSCLC closely related to CCNA2.
network pharmacologyprognosistumor microenvironmentFuzheng Kang'ai FormulaChinese medicinelung adenocarcinoma
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