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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
代海涛,E-mail:48440045@qq.com
收稿日期:2025-04-18,
修回日期:2025-07-05,
纸质出版日期:2025-07-30
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郝小慧,陈敏,仵楠,等.β-arrestin1在口腔鳞状细胞癌中的表达及其对细胞增殖、迁移、侵袭的作用[J].陆军军医大学学报,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.
郝小慧,陈敏,仵楠,等.β-arrestin1在口腔鳞状细胞癌中的表达及其对细胞增殖、迁移、侵袭的作用[J].陆军军医大学学报,2025,47(14):1632-1641.DOI:10.16016/j.2097-0927.202504071. DOI:
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:
目的
2
探讨β-arrestin1(ARRB1)在口腔鳞状细胞癌(oral squamous cell carcinoma,OSCC)中对细胞增殖、迁移和侵袭的作用。
方法
2
基于TCGA数据库分析ARRB1在OSCC中的表达特征,并利用GSEA富集分析表明其可能涉及的信号通路,同时探讨其对OSCC患者预后的潜在影响。进一步通过免疫组化染色评估ARRB1在癌及癌旁组织中的表达差异,结合统计分析ARRB1与临床病理特征的相关性。利用qPCR和Western blot验证ARRB1在SCC-15、CAL-27及HOK中的表达特征。构建ARRB1过表达质粒模型,结合克隆形成、EdU、划痕、Transwell实验分析其对OSCC细胞增殖、迁移和侵袭的影响。
结果
2
TCGA分析显示,ARRB1在HNSC和OSCC组织中的表达水平显著低于正常组织(
P
<
0.01)。ARRB1在OSCC组织中的表达与肿瘤分化程度、淋巴结转移及TNM分期相关(
P
<
0.05)。高表达ARRB1的患者生存率较低表达组高(
HR
=0.50,
P
=0.041),这与生信分析结果一致。经实验验证,SCC-15、CAL-27中ARRB1表达水平低于HOK(
P
<
0.01),且ARRB1过表达显著抑制细胞增殖(
P
<
0.05)、迁移(
P
<
0.01)和侵袭(
P
<
0.01)。
结论
2
ARRB1在OSCC中低表达,过表达ARRB1抑制OSCC细胞增殖、迁移和侵袭,并与患者预后改善相关。
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
its overexpression inhibits the proliferation
migration and invasion of OSCC cells
and it is related to prognosis improvement.
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