HPV16-miR-H1 promotes proliferation, migration, and glycolysis in head and neck squamous cell carcinoma cells via the PTEN/AKT pathway

Human papillomavirus type 16 (HPV16) is the most common type of infection in head and neck squamous cell carcinoma (HNSCC).The HPV16-encoded miRNA, HPV16-miR-H1, has been validated in cervical cancer tissues and cells, but its role in the pathogenesis of HNSCC remains unclear. The expression level of HPV16-miR-H1 in HNSCC cells was detected, and its mechanism of action was analyzed using bioinformatics tools and RNA sequencing. Overexpression and knockdown of HPV16-miR-H1 were performed to validate its regulatory effects on the PTEN/AKT axis and its impact on cell proliferation, migration, the cell cycle, and glycolysis. HPV16-miR-H1 was highly expressed in HPV16-positive HNSCC cells. Bioinformatics prediction and gene enrichment analysis indicated that HPV16-miR-H1 regulates PTEN transcription and the glycolysis process. Dual-luciferase reporter assays further confirmed that HPV16-miR-H1 targets the 3’-UTR region of PTEN. Functional experiments demonstrated that HPV16-miR-H1 affects HNSCC cell proliferation, migration, the cell cycle, and glycolysis. The expression of HPV16-miR-H1 in HNSCC cells was validated for the first time. Further studies revealed that it regulates the PTEN/AKT axis by targeting the 3’UTR region of PTEN, thereby enhancing the proliferation, migration, and glycolytic processes in HNSCC cells.

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Publication Details

Journal
Scientific Reports
Published
2025-12-22
DOI
https://doi.org/10.1038/s41598-025-31764-x
Citations
1
Primary Topic
MicroRNA in disease regulation
Type
article
Field-Weighted Citation Impact
0.94

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article

HPV16-miR-H1 promotes proliferation, migration, and glycolysis in head and neck squamous cell carcinoma cells via the PTEN/AKT pathway

Dezhuan Da, Yuxiu Ma, Shangdong Li, Qi Zhang et al.
1 citations
Scientific Reports
MicroRNA in disease regulation
0.94
article

HPV16-miR-H1 promotes proliferation, migration, and glycolysis in head and neck squamous cell carcinoma cells via the PTEN/AKT pathway

Dezhuan Da, Yuxiu Ma, Shangdong Li, Qi Zhang, XUHUI ZHAO, Shuang Liang, Chunyan Dang, Hongling Li, Ruilin Wang
article en
1 citations

Abstract

Human papillomavirus type 16 (HPV16) is the most common type of infection in head and neck squamous cell carcinoma (HNSCC).The HPV16-encoded miRNA, HPV16-miR-H1, has been validated in cervical cancer tissues and cells, but its role in the pathogenesis of HNSCC remains unclear. The expression level of HPV16-miR-H1 in HNSCC cells was detected, and its mechanism of action was analyzed using bioinformatics tools and RNA sequencing. Overexpression and knockdown of HPV16-miR-H1 were performed to validate its regulatory effects on the PTEN/AKT axis and its impact on cell proliferation, migration, the cell cycle, and glycolysis. HPV16-miR-H1 was highly expressed in HPV16-positive HNSCC cells. Bioinformatics prediction and gene enrichment analysis indicated that HPV16-miR-H1 regulates PTEN transcription and the glycolysis process. Dual-luciferase reporter assays further confirmed that HPV16-miR-H1 targets the 3’-UTR region of PTEN. Functional experiments demonstrated that HPV16-miR-H1 affects HNSCC cell proliferation, migration, the cell cycle, and glycolysis. The expression of HPV16-miR-H1 in HNSCC cells was validated for the first time. Further studies revealed that it regulates the PTEN/AKT axis by targeting the 3’UTR region of PTEN, thereby enhancing the proliferation, migration, and glycolytic processes in HNSCC cells.

Scientific ReportsVol. 15(1)
Gansu University of Traditional Chinese Medicine (CN), Gansu Provincial Hospital (CN)
Fudan University, Natural Science Foundation of Gansu Province, Science and Technology Department of Gansu Province
Openalex Percentile: Top 18%
MicroRNA in disease regulation
0.94
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HPV16-miR-H1 promotes proliferation, migration, and glycolysis in head and neck squamous cell carcinoma cells via the PTEN/AKT pathway — Dezhuan Da, Yuxiu Ma, et al. · Scientific Reports (2025) | TGRS Research Map | TGRS