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ABSTRACT: Objective
This study aimed to elucidate the role of miR-338-3p in cervical cancer, focusing on its regulatory effect on the WAPL (wings apart-like homolog) gene and the consequent influence on the behavior of cervical carcinoma cells.Materials and methods
Bioinformatic analysis identified a potential miR-338-3p binding site in the WAPL 3' untranslated region (3'UTR). This interaction was confirmed using a dual-luciferase reporter assay. The effects of miR-338-3p overexpression on the proliferation, apoptosis, cell cycle, and invasion of cervical cancer cells were subsequently evaluated.Results
WAPL transcript levels were elevated in cervical cancer tissues compared with normal controls (P < 0.05). The GV369/miR-338-3p construct was successfully generated, and qRT-PC
SUBMITTER: Li B
PROVIDER: S-EPMC12797562 | biostudies-literature | 2025 Dec
REPOSITORIES: biostudies-literature