Expression of β-arrestin1 in oral squamous cell carcinoma and its effect on cell proliferation, migration and invasion
Basic Medicine|更新时间:2025-07-25
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Expression of β-arrestin1 in oral squamous cell carcinoma and its effect on cell proliferation, migration and invasion
Journal of Army Medical UniversityVol. 47, Issue 14, Pages: 1632-1641(2025)
作者机构:
1.石河子大学医学院,新疆石河子
2.石河子大学第一附属医院口腔科,新疆石河子
作者简介:
DAI Haitao, E-mail: 48440045@qq.com
基金信息:
the Project of Science and Technology Plan of Xinjiang Production and Construction Corps(2024ZD067);the Scientific Research Project of the First Affiliated Hospital of Shihezi University(LC2023005);the Innovation Project of Resident and Postgraduate Students in the First Affiliated Hospital of Shihezi University(ZP2023083)
HAO X H,CHEN M,WU N,et al.Expression of β-arrestin1 in oral squamous cell carcinoma and its effect on cell proliferation, migration and invasion[J].J Army Med Univ,2025,47(14):1632-1641.DOI:10.16016/j.2097-0927.202504071.
HAO X H,CHEN M,WU N,et al.Expression of β-arrestin1 in oral squamous cell carcinoma and its effect on cell proliferation, migration and invasion[J].J Army Med Univ,2025,47(14):1632-1641.DOI:10.16016/j.2097-0927.202504071.DOI:
Expression of β-arrestin1 in oral squamous cell carcinoma and its effect on cell proliferation, migration and invasion
Objective To investigate the effect of β-arrestin1 (ARRB1) on cell proliferation
migration and invasion in oral squamous cell carcinoma (OSCC). Methods Based on The Cancer Genome Atlas (TCGA) database
the expression profiles of ARRB1 in OSCC were analyzed
and then Gene Set Enrichment Analysis (GSEA) was used to suggest the possible signaling pathways involved
and to explore its potential impact on the prognosis of OSCC patients. Immuinohistochemistry (IHC) was performed to detect the expression of ARRB1 in OSCC tumor tissues and adjacent tissues
and the correlation between ARRB1 expression and clinicopathological features was statistically analyzed. The expression profiles of ARRB1 in SCC-15
CAL-27 and HOK cell lines were verified by qPCR and Western blotting. The ARRB1 overexpression plasmid model was constructed
and its effects on the proliferation
migration and invasion of OSCC cells were analyzed by clone formation
EdU
scratch and Transwell assays. Results TCGA showed that the expression level of ARRB1 was significantly lower in head and neck squamous cell carcinoma (HNSC) and OSCC tissues than the corresponding normal tissues (
P
<
0.01). The expression of ARRB1 in OSCC tissues was correlated with tumor differentiation
lymph node metastasis and TNM stage (
P
<
0.05). The OSCC patients with high expression of ARRB1 had a lower survival rate than those with low expression (
P
<
0.01)
which was consistent with the results of bioinformatics analysis. The expression level of ARRB1 in SCC-15 and CAL-27 cells was lower than that of HOK cells (
P
<
0.01)
and its overexpression significantly inhibited cell proliferation (
P
<
0.05)
migra
tion (
P
<
0.01) and invasion (
P
<
0.01). Conclusion ARRB1 is lowly expressed in OSCC
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