Oct4 activates IL-17A to orchestrate M2 macrophage polarization and cervical cancer metastasis

• Published in: Cancer Immunology, Immunotherapy Immunotherapy, 2024-03, Vol.73 (4), p.73-73, Article 73
• Main Authors: Bian, Zhuoqiong, Wu, Xiaoling, Chen, Qing, Gao, Qing, Xue, Xiang, Wang, Yidong
• Format: Article
• Language: English
• Subjects: Cancer Research; Cervical cancer; Female; Flow cytometry; Humans; Immunology; Inflammatory diseases; Interleukin-17 - metabolism; Invasiveness; Macrophages; Macrophages - metabolism; Medicine; Medicine & Public Health; Metastases; Metastasis; Oct-4 protein; Oncology; Phenotypes; Polarization; Tumors; Uterine Cervical Neoplasms - metabolism
• ISSN: 1432-0851; 0340-7004; 1432-0851
• DOI: 10.1007/s00262-023-03596-z

Background Cervical cancer is a common malignant tumor in the female. Interleukin (IL)-17A is a proinflammatory factor and exerts a vital function in inflammatory diseases and cancers. M2 macrophage has been confirmed to promote tumor development. Nevertheless, it is not yet known whether IL-17A facilitates cervical cancer development by inducing M2 macrophage polarization. Therefore, this study was conducted to investigate the regulatory effect of IL-17A on M2 macrophage polarization and the underlying mechanism in cervical cancer development. Methods RT-qPCR was utilized for testing IL-17A expression in cancer tissues and cells. Flow cytometry was applied to evaluate the M1 or M2 macrophage polarization. Cell proliferative, migratory, and invasive capabilities were measured through colony formation and transwell assays. ChIP and luciferase reporter assays were applied to determine the interaction between IL-17A and octamer-binding transcription factor 4 (OCT4). Results IL-17A expression and concentration were high in metastatic tissues and cells of cervical cancer. IL-17A was found to facilitate M2 macrophage polarization in cervical cancer. Furthermore, IL-17A facilitated the macrophage-mediated promotion of cervical cancer cell proliferative, migratory, and invasive capabilities. Mechanistic assays manifested that Oct4 binds to and transcriptionally activated IL-17A in cervical cancer cells. Furthermore, Oct4 promoted cervical cancer cell malignant phenotype and M2 macrophage polarization by activating the p38 pathway that, in turn, upregulated IL-17A. Additionally, in vivo experiments confirmed that Oct4 knockdown reduced tumor growth and metastasis. Conclusion Oct4 triggers IL-17A to facilitate the polarization of M2 macrophages, which promotes cervical cancer cell metastasis.