SLC8A1-AS1 inhibits oral squamous cell carcinoma by regulating the miR-1305/ESRRG axis

Solute carrier family 8 member A1 antisense RNA 1 (SLC8A1-AS1) is a long non-coding RNA (lncRNA) that has been identified in recent years and is implicated in the progression of various cancers, including glioma and thyroid cancer. However, its role in oral squamous cell carcinoma (OSCC) remains poorly understood. The aim of this study is to investigate the function of SLC8A1-AS1 in OSCC and to explore its potential mechanisms of action. The TCGA database was utilized to analyze the expression and prognostic significance of SLC8A1-AS1 in OSCC. QRT-PCR was employed to measure the gene expression levels of SLC8A1-AS1 and its target genes. CCK-8, EdU staining, wound healing, and Transwell assays were conducted to assess the effects of SLC8A1-AS1 on OSCC cells. Dual-luciferase reporter gene and RNA pull-down assays were performed to verify the interactions between SLC8A1-AS1 and its target genes. Student’s t-test or one-way analysis of variance (ANOVA) was applied for data analysis in this study. SLC8A1-AS1 was found to be downregulated in OSCC tissues and cell lines. Overexpression of SLC8A1-AS1 inhbited the proliferation, migration, and invasion of OSCC cells. Bioinformatics analyses predicted that miR-1305 is a target of SLC8A1-AS1, while ESRRG is a target of miR-1305. Furthermore, the inhibitory effects of SLC8A1-AS1 on the proliferation, migration, and invasion of OSCC cells were reversed by the introduction of miR-1305 mimics. SLC8A1-AS1 inhibits the progression of OSCC by modulating the miR-1305/ESRRG axis.

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Publication Details

Journal
Discover Oncology
Published
2025-09-26
DOI
https://doi.org/10.1007/s12672-025-03586-w
Primary Topic
Cancer-related molecular mechanisms research
Type
article
Field-Weighted Citation Impact
0.00

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article

SLC8A1-AS1 inhibits oral squamous cell carcinoma by regulating the miR-1305/ESRRG axis

Feng Ding, Min Hu, Song Pan, Hongbao Xue
Discover Oncology
Cancer-related molecular mechanisms research
article

SLC8A1-AS1 inhibits oral squamous cell carcinoma by regulating the miR-1305/ESRRG axis

Feng Ding, Min Hu, Song Pan, Hongbao Xue
article en

Abstract

Solute carrier family 8 member A1 antisense RNA 1 (SLC8A1-AS1) is a long non-coding RNA (lncRNA) that has been identified in recent years and is implicated in the progression of various cancers, including glioma and thyroid cancer. However, its role in oral squamous cell carcinoma (OSCC) remains poorly understood. The aim of this study is to investigate the function of SLC8A1-AS1 in OSCC and to explore its potential mechanisms of action. The TCGA database was utilized to analyze the expression and prognostic significance of SLC8A1-AS1 in OSCC. QRT-PCR was employed to measure the gene expression levels of SLC8A1-AS1 and its target genes. CCK-8, EdU staining, wound healing, and Transwell assays were conducted to assess the effects of SLC8A1-AS1 on OSCC cells. Dual-luciferase reporter gene and RNA pull-down assays were performed to verify the interactions between SLC8A1-AS1 and its target genes. Student’s t-test or one-way analysis of variance (ANOVA) was applied for data analysis in this study. SLC8A1-AS1 was found to be downregulated in OSCC tissues and cell lines. Overexpression of SLC8A1-AS1 inhbited the proliferation, migration, and invasion of OSCC cells. Bioinformatics analyses predicted that miR-1305 is a target of SLC8A1-AS1, while ESRRG is a target of miR-1305. Furthermore, the inhibitory effects of SLC8A1-AS1 on the proliferation, migration, and invasion of OSCC cells were reversed by the introduction of miR-1305 mimics. SLC8A1-AS1 inhibits the progression of OSCC by modulating the miR-1305/ESRRG axis.

Discover OncologyVol. 16(1)
Bengbu Medical College (CN), The Second Affiliated Hospital of Bengbu Medical College (CN)
Division of Graduate Education
Openalex Percentile: Top 68%
Cancer-related molecular mechanisms research
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SLC8A1-AS1 inhibits oral squamous cell carcinoma by regulating the miR-1305/ESRRG axis — Feng Ding, Min Hu, et al. · Discover Oncology (2025) | TGRS Research Map | TGRS