He Mudan, Xie Guogang, Shen Fang, Li Xingjing
Department of Respiratory and Critical Care Medicine, Zhongshan Hospital Wusong Branch, Fudan University, Shanghai, 201900, China.
Department of Respiratory and Critical Care Medicine, Shanghai General Hospital, Shanghai JiaoTong University School of Medicine, Shanghai, 200080, China.
Heliyon. 2024 Mar 12;10(6):e27729. doi: 10.1016/j.heliyon.2024.e27729. eCollection 2024 Mar 30.
ANXA2 has been extensively documented in relation to cancer. Nevertheless, the involvement of ANXA2 in lung carcinoma remains uncertain.
Data from The Cancer Genome Atlas (TCGA) database was downloaded using open-access methods. The examination of publicly available data was conducted utilizing the R software. The mRNA level of specific molecules was detected using Real-time Quantitative PCR (qPCR). The protein level of specific molecules was detected using the Western blot assay. The cell proliferation ability of cancer cells was assessed using the CCK8 assay. The invasion and migration capability of cancer cells was assessed using the Transwell assay. Validation of exosomes extraction was conducted using electron microscopy and particle size analysis.
In this study, based on series experiments, we found that ANXA2 can promote the activation of neuroastrocytes cells CP-H122 through the exosome pathway. Also, we found that ANXA2 can be transmitted from A549 cells to CP-H122 through the exosomes pathway and further promote the activation of CP-H122. Activated CP-H122 cells further enhance the proliferation, invasion and metastasis of A549 cells. Meanwhile, we performed transcriptome sequencing to explore the downstream genes of ANXA2 to screen potential targets for follow-up studies. Analysis based on public data showed that ANXA2 was related to the worse survival performance and clinical features of lung cancer. Gene set enrichment analysis based on the Hallmark gene set indicated that the patient with high ANXA2 expression might have a higher activity of the apical surface, reactive oxygen species pathway, angiogenesis, TGF-β signaling, MYC target, but lower activity of pancreas-β cells. More important, our results showed that ANXA2 can affects immunotherapy response and reshape immune microenvironment of lung cancer.
This study demonstrates that ANXA2 activates CP-H122 cells, affects A549 cell behavior, and impacts lung cancer prognosis and immunotherapy response.
关于膜联蛋白A2(ANXA2)与癌症的关系已有大量文献记载。然而,ANXA2在肺癌中的作用仍不明确。
使用开放获取方法从癌症基因组图谱(TCGA)数据库下载数据。利用R软件对公开可用数据进行分析。采用实时定量聚合酶链反应(qPCR)检测特定分子的mRNA水平。使用蛋白质免疫印迹法检测特定分子的蛋白质水平。采用细胞计数试剂盒-8(CCK8)法评估癌细胞的增殖能力。采用Transwell法评估癌细胞的侵袭和迁移能力。通过电子显微镜和粒度分析对外泌体提取进行验证。
在本研究中,基于一系列实验,我们发现ANXA2可通过外泌体途径促进神经星形胶质细胞CP-H122的激活。此外,我们发现ANXA2可通过外泌体途径从A549细胞传递至CP-H122,并进一步促进CP-H122的激活。激活的CP-H122细胞进一步增强A549细胞的增殖、侵袭和转移能力。同时,我们进行了转录组测序以探索ANXA2的下游基因,从而筛选后续研究的潜在靶点。基于公开数据的分析表明,ANXA2与肺癌较差的生存表现和临床特征相关。基于标志性基因集的基因集富集分析表明,ANXA2高表达的患者可能具有更高的顶表面、活性氧途径、血管生成、转化生长因子-β信号传导、MYC靶点活性,但胰腺β细胞活性较低。更重要的是,我们的结果表明ANXA2可影响肺癌的免疫治疗反应并重塑免疫微环境。
本研究表明,ANXA2激活CP-H122细胞,影响A549细胞行为,并影响肺癌预后和免疫治疗反应。