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Wnt信号通路调节肺癌干细胞的干性,其抑制剂对肺癌SPC-A1细胞具有抗癌作用。

Wnt signaling regulates the stemness of lung cancer stem cells and its inhibitors exert anticancer effect on lung cancer SPC-A1 cells.

作者信息

Zhang Xueyan, Lou Yuqing, Wang Huimin, Zheng Xiaoxuan, Dong Qianggang, Sun Jiayuan, Han Baohui

机构信息

Department of Pulmonary Medicine, Shanghai Chest Hospital, Shanghai Jiao Tong University, 241 West Huaihai Road, Shanghai, 200000, China.

出版信息

Med Oncol. 2015 Apr;32(4):95. doi: 10.1007/s12032-014-0462-1. Epub 2015 Mar 3.

Abstract

Wnt signaling plays an important role in regulating the activity of cancer stem cells (CSCs) in a variety of cancers. In this study, we explored the role of Wnt signaling in the lung cancer stem cells (LCSCs). LCSCs were obtained by sphere culture, for which human lung adenocarcinoma cell line SPC-A1 was treated with IGF, EGF and FGF-10. The stemness of LCSCs was confirmed by immunofluorescence, and pathway analysis was performed by functional genome screening and RT-PCR. The relationship between the identified signaling pathway and the expression of the stemness genes was explored by agonist/antagonist assay. Moreover, the effects of different signaling molecule inhibitors on sphere formation, cell viability and colony formation were also analyzed. The results showed that LCSCs were successfully generated as they expressed pluripotent stem cell markers Nanog and Oct 4, and lung distal epithelial markers CCSP and SP-C, by which the phenotype characterization of stem cells can be confirmed. The involvement of Wnt pathway in LCSCs was identified by functional genome screening and verified by RT-PCR. The expression of Wnt signaling components was closely related to the expression of the Nanog and Oct 4. Furthermore, targeting Wnt signaling pathway by using different signaling molecule inhibitors can exert anticancer effects. In conclusion, Wnt signaling pathway is involved in the stemness regulation of LCSCs and might be considered as a potential therapeutic target in lung adenocarcinoma.

摘要

Wnt信号通路在多种癌症中对癌症干细胞(CSCs)活性的调节起着重要作用。在本研究中,我们探究了Wnt信号通路在肺癌干细胞(LCSCs)中的作用。通过球体培养获得LCSCs,为此将人肺腺癌细胞系SPC-A1用胰岛素样生长因子(IGF)、表皮生长因子(EGF)和碱性成纤维细胞生长因子-10(FGF-10)进行处理。通过免疫荧光确认LCSCs的干性,并通过功能基因组筛选和逆转录聚合酶链反应(RT-PCR)进行通路分析。通过激动剂/拮抗剂试验探究已鉴定的信号通路与干性基因表达之间的关系。此外,还分析了不同信号分子抑制剂对球体形成、细胞活力和集落形成的影响。结果显示,成功生成了LCSCs,因为它们表达多能干细胞标志物Nanog和Oct 4,以及肺远端上皮标志物克拉拉细胞分泌蛋白(CCSP)和表面活性蛋白C(SP-C),据此可确认干细胞的表型特征。通过功能基因组筛选确定了Wnt通路在LCSCs中的参与,并通过RT-PCR进行了验证。Wnt信号成分的表达与Nanog和Oct 4的表达密切相关。此外,使用不同信号分子抑制剂靶向Wnt信号通路可发挥抗癌作用。总之,Wnt信号通路参与LCSCs的干性调节,可能被视为肺腺癌的一个潜在治疗靶点。

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