E2F4 may be a core transcription factor in the lncRNA‐TF regulatory network in cervical cancer

BACKGROUND: Cervical cancer is the most common gynecological cancer worldwide and is associated with high morbidity and mortality. Despite improvements in therapeutic strategies, the network regulation mechanism remains unclear and the treatment effect is not satisfactory. Therefore, there is a need to continue studying the mechanism of cervical cancer to explore effective gene targets and precise targeted therapy drugs. METHODS: First, three paired tissues (cancer tissues and noncancerous tissues) from patients with cervical squamous cell carcinoma were collected, grouped, and analyzed by microarray. Second, differentially expressed mRNAs (DEMs) and differentially expressed lncRNAs (DELs) (|fold change| ≥ 2 and p < 0.05) between the two groups were screened. For DEMs, functional annotation and pathway analysis were performed using DAVID. Functional prediction of DELs was then performed and their cis‐regulatory and trans‐regulatory networks were explored. RESULTS: Function prediction of DELs (both up‐regulated and down‐regulated) shows that the highest frequency Cellular Component (CC) item is cytosol, the highest frequency Molecular function (MF) item is mitotic cell cycle and the highest frequency Biological Process (BP) item is protein binding. Through cis‐regulation analysis of DELs, the cis‐regulatory relationship of 96 DELs was predicted. The lncRNA‐trans‐regulation network analysis suggested that E2F4 may be the core transcription factor in the lncRNA‐TF regulatory network in cervical cancer. CONCLUSIONS: The lncRNA‐TF regulatory network plays an important role in the occurrence and progression of cervical cancer, and E2F4 may be a critical transcription factor in the regulatory network.