FBXO39 predicts poor prognosis and correlates with tumor progression in cervical squamous cell carcinoma

免疫组织化学 免疫印迹 癌变 单变量分析 癌症研究 污渍 癌症 伤口愈合 病理 生物 细胞迁移 医学 细胞 内科学 免疫学 多元分析 基因 生物化学 遗传学
作者
Yanru Yang,Yun Zhao,Guorui Sun,Sai‐Jie Zuo,Jia Chai,Tianqi Xu,Jin Liu,Lingfei Li,Junyang Song,Shoubin Qian,Yulin Kang,Fang Sui,Mingyang Li,Qingge Jia
出处
期刊:Pathology Research and Practice [Elsevier BV]
卷期号:238: 154090-154090 被引量:5
标识
DOI:10.1016/j.prp.2022.154090
摘要

Cancer/testis antigen (CTA) is a class of antigen molecules mainly expressed in the germinal epithelium of testis and some tumor tissues. FBXO39, also known as F-box protein 39, is a crucial CTA molecule. F-box protein 39 (FBXO39) is overexpressed in cervical squamous cell carcinomas (CESCs), however its function in cancer development and clinical significance are still unknown.We used paraffin-embedded tumor tissues from 124 patients and fresh-harvested and paired adjacent normal esophageal tissues from 15 CESC patients who underwent primary surgical resection in Xijing Hospital between 2015 and 2020. The expression level of FBXO39 was evaluated through immunohistochemistry, Western Blot and q-PCR. Prognostic and survival analyses were conducted using univariate/multivariate analysis and log-rank analysis with SPSS 23.0. CCK-8, wound-healing and Transwell assays were applied to demonstrate that FBXO39 promoted the proliferation, migration and invasion. Finally, we constructed a xenografts model of the C-33A cell lines to observe the effect of FBXO39 on tumorigenesis in vivo.Immunohistochemical results showed that FBXO39 was highly expressed in cancer tissues than in corresponding non-cancer tissues. Similarly, we proved this result at protein and mRNA level by Western-Blotting and q-PCR. Prognostic and OS analyses showed that the FBXO39 expression level was an individual prognostic factor in CESC patients. CCK-8, wound-healing and Transwell assays proved that the overexpression of FBXO39 in Si-Ha cells promoted the proliferation, migration and invasion of the cells. Knocking down FBXO39 in C-33A cells inhibited the proliferation, migration and invasion of cells. The experimental results of xenografts model in nude mice showed that the knockdown of FBXO39 in C-33A cells slowed down the growth of tumor.FBXO39 is a poor prognostic factor of cervical squamous cell carcinoma, which may provide a novel therapeutic target for CESC.
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