Open Access

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

  • Authors:
    • Gladys Wendy Valente‑Niño
    • Hilda Jiménez‑Wences
    • Manuel Joaquín Romero‑López
    • Judit Alarcón‑Millán
    • Miguel Ángel Mendoza‑Catalán
    • Oscar Peralta‑Zaragoza
    • Daniel Hernández‑Sotelo
    • Carlos Pérez‑Plasencia
    • Gloria Fernández‑Tilapa
  • View Affiliations

  • Published online on: June 20, 2025     https://doi.org/10.3892/mmr.2025.13600
  • Article Number: 235
  • Copyright: © Valente‑Niño et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

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Abstract

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. SLC7A1 was found among the shared targets, SGK1 among the targets of miR‑124‑3p and HMGB2 as a target of miR‑23b‑3p. SLC7A1, SGK1 and HMGB2 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. SLC7A1, SGK1 and HMGB2 interact with proteins involved in cellular processes associated with cancer progression. Overexpression of miR‑124‑3p decreased mRNA of SLC7A1 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. HMGB2 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.
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September-2025
Volume 32 Issue 3

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Online ISSN:1791-3004

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Spandidos Publications style
Valente‑Niño GW, Jiménez‑Wences H, Romero‑López MJ, Alarcón‑Millán J, Mendoza‑Catalán MÁ, Peralta‑Zaragoza O, Hernández‑Sotelo D, Pérez‑Plasencia C and Fernández‑Tilapa G: <em>SLC7A1</em>, <em>SGK1</em> and <em>HMGB2</em> are overexpressed in cervical cancer tissues and the miR‑23b‑3p/HMGB2 axis regulates cell migration and invasion. Mol Med Rep 32: 235, 2025.
APA
Valente‑Niño, G.W., Jiménez‑Wences, H., Romero‑López, M.J., Alarcón‑Millán, J., Mendoza‑Catalán, M.Á., Peralta‑Zaragoza, O. ... Fernández‑Tilapa, G. (2025). <em>SLC7A1</em>, <em>SGK1</em> and <em>HMGB2</em> are overexpressed in cervical cancer tissues and the miR‑23b‑3p/HMGB2 axis regulates cell migration and invasion. Molecular Medicine Reports, 32, 235. https://doi.org/10.3892/mmr.2025.13600
MLA
Valente‑Niño, G. W., Jiménez‑Wences, H., Romero‑López, M. J., Alarcón‑Millán, J., Mendoza‑Catalán, M. Á., Peralta‑Zaragoza, O., Hernández‑Sotelo, D., Pérez‑Plasencia, C., Fernández‑Tilapa, G."<em>SLC7A1</em>, <em>SGK1</em> and <em>HMGB2</em> are overexpressed in cervical cancer tissues and the miR‑23b‑3p/HMGB2 axis regulates cell migration and invasion". Molecular Medicine Reports 32.3 (2025): 235.
Chicago
Valente‑Niño, G. W., Jiménez‑Wences, H., Romero‑López, M. J., Alarcón‑Millán, J., Mendoza‑Catalán, M. Á., Peralta‑Zaragoza, O., Hernández‑Sotelo, D., Pérez‑Plasencia, C., Fernández‑Tilapa, G."<em>SLC7A1</em>, <em>SGK1</em> and <em>HMGB2</em> are overexpressed in cervical cancer tissues and the miR‑23b‑3p/HMGB2 axis regulates cell migration and invasion". Molecular Medicine Reports 32, no. 3 (2025): 235. https://doi.org/10.3892/mmr.2025.13600