<i>SLC7A1</i>, <i>SGK1</i> and <i>HMGB2</i> are overexpressed in cervical cancer tissues and the miR‑23b‑3p/HMGB2 axis regulates cell migration and invasion

MicroRNA (miRNA/miR)‑124‑3p and miR‑23b‑3p are tumor suppressor miRNAs that are associated with advanced cervical cancer (CC), regulating proliferation, migration, invasion, apoptosis and metastasis; however, the identity and function of the various genes regulated by these miRNAs remain unknown. The present study predicted the specific and shared targets of miR‑124‑3p and miR‑23b‑3p, cellular processes and signaling pathways involving the predicted targets. <i>SLC7A1</i> was found among the shared targets, <i>SGK1</i> among the targets of miR‑124‑3p and <i>HMGB2</i> as a target of miR‑23b‑3p. <i>SLC7A1</i>, <i>SGK1</i> and <i>HMGB2</i> mRNA expression was markedly increased in patients with cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC) and levels of SGK1 and HMGB2 were associated with CC progression. <i>SLC7A1</i>, <i>SGK1</i> and <i>HMGB2</i> interact with proteins involved in cellular processes associated with cancer progression. Overexpression of miR‑124‑3p decreased mRNA of <i>SLC7A1</i> in C‑33A cells, and of SGK1 in both cell lines. Ectopic expression of miR‑23b‑3p decreased HMGB2 levels in C‑33A and CaSki, and reduced cell migration and invasion. <i>HMGB2</i> knockdown experiments revealed that HMGB2 modulates migration and invasion of CC cell lines. In conclusion, the results of the present study suggest that miR‑124‑3p and miR‑23b‑3p modulate processes associated with carcinogenesis and tumor progression through their individual and shared target mRNAs and that the miR‑23b‑3p/HMGB2 axis is among the mechanisms that modulate migration and invasion in CC.